-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, V/iyFKZrSecVi8HmkVjVceOOVs9ZCjtRhadK7CVciFiM3AFqe44IchWoGO1P0wCS +Dmx8Chx4TZAYZjvEHGwjQ== 0001108017-06-000568.txt : 20060810 0001108017-06-000568.hdr.sgml : 20060810 20060810095220 ACCESSION NUMBER: 0001108017-06-000568 CONFORMED SUBMISSION TYPE: 10QSB PUBLIC DOCUMENT COUNT: 5 CONFORMED PERIOD OF REPORT: 20060630 FILED AS OF DATE: 20060810 DATE AS OF CHANGE: 20060810 FILER: COMPANY DATA: COMPANY CONFORMED NAME: Worldwide Biotech & Pharmaceutical CO CENTRAL INDEX KEY: 0000095302 STANDARD INDUSTRIAL CLASSIFICATION: WHOLESALE-GROCERIES & RELATED PRODUCTS [5140] IRS NUMBER: 590950777 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10QSB SEC ACT: 1934 Act SEC FILE NUMBER: 001-06914 FILM NUMBER: 061019691 BUSINESS ADDRESS: STREET 1: 110 SARASOTA QUAY CITY: SARASOTA STATE: FL ZIP: 34236 BUSINESS PHONE: 941-365-2521 MAIL ADDRESS: STREET 1: 110 SARASOTA QUAY CITY: SARASOTA STATE: FL ZIP: 34236 FORMER COMPANY: FORMER CONFORMED NAME: SUN CITY INDUSTRIES INC DATE OF NAME CHANGE: 19920703 FORMER COMPANY: FORMER CONFORMED NAME: SUN CITY DAIRY PRODUCTS INC DATE OF NAME CHANGE: 19690727 10QSB 1 wwbio10qsb.htm 10-QSB 10-QSB
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 


Form 10-QSB
 


[X] QUARTERLY REPORT UNDER SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF 1934: For the quarterly period ended June 30, 2006

[ ] TRANSITION REPORT UNDER SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF1934: For the transition period from______ to _______

01-06914
Commission File Number

Worldwide Biotech & Pharmaceutical Company
(Name of small business issuer in its charter)
 
Delaware
 
59-0950777
(State or other jurisdiction of Incorporation)
 
(IRS Employer Identification Number)
     
4 Fenghui South Road, 15th Floor, A10-11501     
Jie Zuo Mansion, Xi’an, Shaanxi,
P.R. China 710075  
 
  
86-29-88193339 
 (Address of principal executive offices)     (Issuer’s telephone number) 
 
Check whether the issuer (1) filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes [X] No [ ]

The number of shares outstanding of each of the Issuer’s classes of common equity, as of the latest practicable date: As of June 30, 2006, there were 40,357,502 shares of the common stock issued and outstanding.

Indicate by check mark whether the Registrant is a shell company (as defined in Rule 12b-2 of the Securities Exchange Act of 1934) (check one): Yes [  ]   No [X]
 
Transitional Small Business Disclosure Format (check one): Yes [   ]   No [X]
 
-1-

PART I - FINANCIAL INFORMATION

Item 1. Financial Statements

WORLDWIDE BIOTECH & PARMACEUTICAL COMPANY AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
June 30, 2006
(Unaudited)

ASSETS
     
       
CURRENT ASSETS:
     
    Cash
$
89,381
 
    Marketable securities
 
512,446
 
    Accounts receivable, net of allowance for doubtful accounts of
 
173,018
 
    Inventories
 
435,654
 
    Prepayments and other current assets
 
144,799
 
       
        Total Current Assets
 
1,355,298
 
       
PROPERTY AND EQUIPMENT - Net
 
4,724,565
 
       
LICENSES, net
 
457,750
 
       
LAND USE RIGHTS, net
 
1,394,471
 
       
        Total Assets
$
7,932,084
 
       
       
LIABILITIES AND STOCKHOLDERS' EQUITY
     
       
CURRENT LIABILITIES:
     
    Loans payable
$
1,484,182
 
    Mortgages payable
 
31,430
 
    Note payable - stockholder
 
425,303
 
    Accounts payable
 
894,325
 
    Due to related parties
 
2,032,658
 
    Other current liabilities
 
199,806
 
 
     
        Total Current Liabilities
 
5,067,704
 
       
MORTGAGES PAYABLE, less current portion
 
221,599
 
       
NOTE PAYABLE
 
1,250,891
 
       
MINORITY INTEREST
 
535,363
 
       
        Total Liabilities
 
7,075,557
 
       
STOCKHOLDERS' EQUITY:
     
    Common stock ($.001 par value; 90,000,000 shares authorized;
 
40,358
 
        40,357,502 shares issued and outstanding)
     
    Additional paid-in capital
 
10,799,993
 
    Accumulated deficit
 
(9,094,289
)
    Deferred compensation
 
(774,000
)
    Accumulated other comprehensive loss:
     
    Change in unrealized loss on marketable securities
 
(160,327
)
    Foreign currency translation gain
 
44,792
 
       
        Total Stockholders' Equity
 
856,527
 
       
        Total Liabilities and Stockholders' Equity
$
7,932,084
 

See notes to consolidated financial statements.

-2-


WORLDWIDE BIOTECH & PARMACEUTICAL COMPANY AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
(unaudited)

   
For The Three Months Ended
 
For The Six Months Ended
 
 
 
June 30,
 
June 30,
 
 
 
2006
 
2005
 
2006
 
2005
 
NET REVENUES
 
$
91,312
 
$
-
 
$
202,633
 
$
-
 
                           
COST OF GOODS SOLD
   
78,074
   
-
   
184,091
   
-
 
                           
GROSS PROFIT
   
13,238
   
-
   
18,542
   
-
 
                           
OPERATING EXPENSES:
                         
    Selling expenses
   
34,493
   
-
   
46,864
    -  
    Research and development
   
15,036
   
-
   
29,328
   
55,075
 
    Professional fees
   
21,312
   
38,607
   
101,749
   
67,468
 
    Stock-based compensation
   
249,500
   
1,216,106
   
599,000
   
2,475,628
 
    General and administrative
   
194,012
   
95,594
   
361,694
   
168,631
 
                           
        Total Operating Expenses
   
514,353
   
1,350,307
   
1,138,635
   
2,766,802
 
                           
LOSS FROM OPERATIONS
   
(501,115
)
 
(1,350,307
)
 
(1,120,093
)
 
(2,766,802
)
                           
OTHER INCOME (EXPENSE):
                         
    Interest income
   
43
   
-
   
117
   
2,809
 
    Interest expense
   
(62,429
)
 
(19,672
)
 
(141,918
)
 
(66,703
)
    Other income (exense)
   
(412
)
 
43,791
   
14,672
   
43,791
 
                           
        Total Other Income (Expense)
   
(62,798
)
 
24,119
   
(127,129
)
 
(20,103
)
                           
LOSS BEFORE MINORITY INTEREST
   
(563,913
)
 
(1,326,188
)
 
(1,247,222
)
 
(2,786,905
)
                           
MINORITY INTEREST
   
135,842
   
-
   
135,842
   
-
 
                           
NET LOSS
   
(428,071
)
 
(1,326,188
)
 
(1,111,380
)
 
(2,786,905
)
                           
OTHER COMPREHENSIVE INCOME
                         
    Change in unrealized loss on marketable securities
   
242,932
   
(90,560
)
 
277,419
   
(90,560
)
    Foreign currency translation gain
   
374
   
-
   
14,435
   
-
 
                           
COMPREHENSIVE LOSS
 
$
(184,765
)
$
(1,416,748
)
$
(819,526
)
$
(2,877,465
)
                           
NET LOSS PER COMMON SHARE - BASIC AND DILUTED:
                         
    Net loss per common share
 
$
(0.01
)
$
(0.04
)
$
(0.03
)
$
(0.08
)
                           
    Weighted Common Shares Outstanding - basic and diluted
   
40,357,502
   
37,859,300
   
40,283,979
   
36,565,389
 

See notes to consolidated financial statements.
-3-


WORLDWIDE BIOTECH AND PHARMACEUTICAL COMPANY AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
 

CASH FLOWS FROM OPERATING ACTIVITIES:
             
Net loss
 
$
(1,111,380
)
$
(2,786,905
)
Adjustments to reconcile net loss to net cash used in
             
operating activities: 
             
Depreciation and amortization 
   
192,820
   
46,567
 
Stock-based compensation 
   
599,000
   
2,475,628
 
Minority interest 
   
(135,842
)
 
-
 
Changes in assets and liabilities:
             
Accounts receivable 
   
(29,540
)
 
-
 
Inventories 
   
(75,042
)
 
-
 
Prepayments and other current assets 
   
8,927
   
(695,839
)
Accounts payable 
   
(85,631
)
 
44,230
 
Other current liabilities 
   
(10,863
)
 
30,165
 
               
NET CASH USED IN OPERATING ACTIVITIES
   
(647,551
)
 
(886,154
)
               
CASH FLOWS FROM INVESTING ACTIVITIES:
             
Cash used for business acquisitions
   
(425,303
)
 
-
 
Cash received from business acquisitions
   
13,784
   
-
 
Purchase of property and equipment
   
(14,382
)
 
(230,797
)
               
NET CASH USED IN INVESTING ACTIVITIES
   
(425,901
)
 
(230,797
)
               
CASH FLOWS FROM FINANCING ACTIVITIES:
             
Proceeds from loan payable
   
600,428
   
-
 
Payments on loan payable
   
(625,446
)
 
(60,911
)
Proceeds from note payable - stockholder
   
425,303
   
-
 
Payments on mortgages payable
   
(17,501
)
 
(13,563
)
Proceeds from stockholders/officers
   
685,544
   
363,507
 
               
NET CASH PROVIDED BY FINANCING ACTIVITIES
   
1,068,328
   
289,033
 
               
EFFECT OF EXCHANGE RATE CHANGES ON CASH
   
(65
)
 
-
 
               
NET DECREASE IN CASH
   
(5,189
)
 
(827,918
)
               
CASH at beginning of period
   
94,570
   
1,047,675
 
               
CASH at end of period
 
$
89,381
 
$
219,757
 
               
SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION:
             
 Interest paid
 
$
139,407
 
$
66,703
 

See notes to consolidated financial statements.
-4-

WORLDWIDE BIOTECH & PHARMACEUTICAL COMPANY AND SUBSIDIARIES
NOTES TO FINANCIAL STATEMENTS
June 30, 2006
(UNAUDITED)

NOTE 1 - BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of Presentation

The accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles for interim financial information and with the instructions to Form 10-QSB and Item 310(b) of Regulation S-B. Accordingly, the financial statements do not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. In the opinion of management, all adjustments considered necessary for a fair presentation have been included and such adjustments are of a normal recurring nature. These consolidated financial statements should be read in conjunction with the financial statements for the year ended December 31, 2005 and notes thereto contained in the Report on Form 10-KSB of Worldwide Biotech & Pharmaceutical Company (the “Company” or “Worldwide”) as filed with the Securities and Exchange Commission (the “Commission”). The results of operations for the six months ended June 30, 2006 are not necessarily indicative of the results for the full fiscal year ending December 31, 2006.

The consolidated statements include all the accounts of Worldwide Biotech & Pharmaceutical Company and its wholly-owned and majority-owned subsidiaries. All significant intercompany balances and transactions have been eliminated.

The Company

Worldwide Biotech & Pharmaceutical Company was incorporated in Delaware in 1961. In the forth quarter of 2005, the Company commenced revenue producing operations.

On January 19, 2006, Worldwide by and through its wholly owned subsidiary, Yangling Daiying Biological Engineering Co., Ltd. (“Daiying”), entered into a Reorganization Agreement with Hunan Hua Yang Pharmaceutical Co. Ltd. (“Hua Yang”) and its shareholders.

Pursuant to this agreement, the Company issued 482,800 shares of its common stock to the shareholders of Hua Yang to acquire 51%.
-5-

Also on January 19, 2006, Daiying entered into a Reorganization Agreement with Hunan Ze An Pharmaceutical Co. Ltd. (“Ze An”) and its shareholders. Daiying paid Reminbi (“RMB”) 3,400,000 (Equivalent to US $425,303 at June 30, 2006) and 217,600 shares of common stock of Worldwide for 65% of Ze An.

Revenue recognition

The Company follows the guidance of the Securities and Exchange Commission’s Staff Accounting Bulletin 104 for revenue recognition.  In general, the Company records revenue when persuasive evidence of an arrangement exists, services have been rendered or product delivery has occurred, the sales price to the customer is fixed or determinable, and the likelihood of collection is reasonably assured. Persuasive evidence of an arrangement is demonstrated via purchase order from the distributor, our customer; product delivery is evidenced by the warehouse shipping log as well as signed bill of lading from the trucking company and no product return is allowed except defective or damaged products;; the sales price to the customer is fixed upon acceptance of purchase order; and there are no separate sales rebates, discounts, or volume incentives. The Company manufactures and distributes traditional Chinese medicine, including drink tablets, synthetic medicine, antibiotics, biotech medicine and biotech reagents; wholesale Class II medical devices, Class III medical devices, including but not limited to, medical sewing materials and bond, medical high molecular materials and products, and disposable sterile medical devices. The majority of the Company's revenue derives from sales contracts with distributors.. The Company sells certain products to certain customers on consignment. The Company records revenue for consignment transactions when the consignee sells the product to the end user.
-6-

NOTE 2 - ACQUISITIONS

Operations of the acquired companies have been included in the Company’s operations from the date of the acquisitions.

Pro Forma Results
The following unaudited pro forma financial information presents the combined results of operations of the Company, Hua Yang and Ze An for the three months and six months ended June 30, 2005, as if the acquisitions had occurred on January 1, 2005. The unaudited pro forma financial information is not intended to represent or be indicative of the Company’s consolidated results of operations that would have been reported had the acquisitions been completed on January 1, 2005 and should not be taken as indicative of the Company’s future consolidated results of operations. The unaudited pro forma financial information for the six months ended June 30, 2006 is not presented because the results would be immaterially different that what is currently reported.
 
   
For The Three Months Ended June 30, 2005
 
For The Six Months Ended June 30, 2005
 
           
Revenues
 
$
102,689
 
$
214,146
 
               
Net loss
 
$
(1,416,925
)
$
(2,904,903
)
               
Basic loss per share
 
$
(0.04
)
$
(0.08
)
 
             
               

NOTE 3 - INVENTORIES

Inventories at June 30, 2006, consisted of the following:

Raw materials  
 
$
144,752
 
Work in progress  
   
40,282
 
Finished goods  
   
250,620
 
   
$
435,654
 

-7-

NOTE 4 - LOANS PAYABLE

At June 30, 2006, loans payable consisted of the following:

       
Loan payable, unsecured, payable to a financial institution, guaranteed by an independent third party, with interest at 7.254% per annum payable monthly, with principal due October 26, 2006.
 
$
875,624
 
         
Loans payable, to certain employees, with interest at 14.4% per annum. Such amounts are due on demand.
   
8,130
 
         
Loan payable, unsecured, payable to a financial institution, with interest at 7.02% per annum payable monthly, with principal due May 21, 2007 and collateralized by substantially all of Ze An’s equipment, buildings and land use rights.
   
600,428
 
         
Total
 
$
1,484,182
 

NOTE 5 - RELATED PARTY TRANSACTIONS

Due to related parties

The Chief Executive Officer and a shareholder, from time to time, provided advances to the Company for operating expenses. These advances are short-term in nature and non-interest bearing, payable upon request. The amount due to these related parties at June 30, 2006 was $2,032,658.
-8-

Item 2. Management’s Discussion and Analysis or Plan of Operation

The following analysis of the Company’s results of operations and financial condition should be read in conjunction with the financial statements of Worldwide Biotech & Pharmaceutical Company for the year ended December 31, 2005 and notes thereto contained in Report on Form 10-KSB of Worldwide Biotech & Pharmaceutical Company as filed with the Securities and Exchange Commission.

This report on Form 10-QSB contains certain forward-looking statements including, among others, anticipated trends in our financial condition and results of operations and our business strategy. These forward-looking statements are based largely on our current expectations and are subject to a number of risks and uncertainties. Actual results could differ materially from these forward-looking statements. Important factors to consider in evaluating such forward-looking statements include (i) changes in external factors or in our internal budgeting process which might impact trends in our results of operations; (ii) unanticipated working capital or other cash requirements; (iii) changes in our business strategy or an inability to execute our strategy due to unanticipated changes in the industries in which we operate; and (iv) various competitive market factors that may prevent us from competing successfully in the marketplace.

Critical Accounting Policies

A summary of significant accounting policies is included in Note 1 to the audited financial statements included in Form 10-KSB as filed with the Securities and Exchange Commission for the year ended December 31, 2005. Management believes that the application of these policies on a consistent basis enables us to provide useful and reliable financial information about the company's operating results and financial condition.

The discussion and analysis of our financial condition and results of operations are based upon our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of these consolidated financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an on-going basis, we evaluate our estimates based on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.

 
-9-

Results of Operations

The Company is a high-tech biopharmaceutical company that specializes in the development and potential marketing of viruses/viral vectors, bio-medicines, external diagnostic reagents, prophylactic vaccines for humans, and oral dosage forms of traditional Chinese medicine. The principal products include Hepatitis C virus produced in vitro, ELISA kits for HCV antibody detection, Rapid Test (Colloid Gold Method), Oral dosage forms of traditional Chinese medicine healthcare products and medical devices distributed for other companies.

The Company established its drug-screening assay based on its in vitro cell culture system, and initiated drug screening for anti-HCV therapeutics and commenced revenue producing operations through its majority owned subsidiary, Shaanxi Daiying Medicine Distribution Co., Ltd. (“Shaanxi”) in the fourth quarter of 2005.

Shaanxi distributes traditional Chinese medicine including drink tablets, synthetic medicine, antibiotics, biotech medicine and biotech reagents, wholesale Class II medical devices, Class III medical devices, including but not limited to, medical sewing materials and bond, medical high molecular materials and products, and disposable sterile medical devices.

The Company obtained SFDA approvals for three of its oral traditional Chinese medicines, including a liver-care medicine, an anti-cold medicine and a cough-suppressant prior to year end of 2005. The production and sales for these products commenced during the first quarter of 2006.

The Company through Daiying acquired Hunan Hua Yang Pharmaceutical Co., Ltd. (Hua Yang) and Hunan Ze An Pharmaceutical Co., Ltd. (Ze An) on January 19, 2006. Hua Yang currently holds 23 medicines with National Drug Production Licenses and 5 nutrient supplements with National Food Production Licenses. Daiying controls 51% of the total shares of Hua Yang. Ze An currently holds 5 product lines, 10 medicines with National Drug Production Licenses and 1 nutrient supplement with a National Food Production License. Daiying controls 65% of the total shares of Ze An.

In 2005, the Company entered into a sole distribution agreement with TARAMEDIC.CORPORATION.BHD, a Malaysian company, to distribute its Tara KLamp® Disposable Circumcision Device. TARAMEDIC owns patents both in Malaysia and China. The Company obtained the regulation approval for this product from Chinese SFDA on January 26, 2006 and sales have commenced.

The following analysis shows the selected unaudited consolidated statement of operations data of the Company for the six month period ended June 30, 2006 and June 30, 2005. The data should be read in conjunction with the unaudited consolidated financial statements of the Company for the six month period ended June 30, 2006 and June 30, 2005 and related notes thereto. 

 
-10-

Results of operations for the six months ended June 30, 2006 as compared to the six months ended June 30, 2005

Revenues

For the six months ended June 30, 2006, our revenues were $202,633 as compared to $0 for the six months ended June 30 2005, an increase of $202,633. We attribute this increase in net revenues to the Company’s establishment of its drug-screening assay (based on its in vitro cell culture system), and initiated drug screening for anti-HCV therapeutics, to an increased marketing effort, to the gradual acceptance of Shaanxi distribution network and to revenues generated from Hua Yang and Ze An, majority owned subsidiaries the Company acquired on January 19, 2006. The Company was a development stage company prior to June 30, 2005.

Cost of Sales and Gross Profit

For the six months ended June 30, 2006, cost of sales amounted to $184,091 as compared to cost of sales of $0 for the six months ended June 31, 2005. Gross profit for the six months ended June 30, 2006 was $18,542 or 9.2% of revenues, as compared to $0 for the six months ended June 30, 2005.

Operating Expenses

For the six months ended June 30, 2006, total operating expenses were $1,138,635 as compared to $2,766,802 for the six months ended June 30, 2005, a decrease of $1,628,167, or approximately 58.8%.

Included in this decrease was:

 
·
For the six months ended June 30, 2006, we incurred selling expense of $46,864 compared to $0 for the six months ended June 30, 2005. The increase was due to an increased marketing effort of Shaanxi and selling activities from Hua Yang and Ze An, majority owned subsidiaries the Company acquired on January 19, 2006.
 
·
For the six months ended June 30, 2006, we incurred research and development expense of $29,328 compared to $55,075 for the six months ended June 30, 2005, a decrease of $25,747 or (46.7%). The decrease was due to regulatory approval of certain major products of the Company.
 
·
For the six months ended June 30, 2006, we incurred professional fees of $101,749 as compared to $67,468 for the six months ended June 30, 2005, an increase of $34,281, or 50.8%. The increase was due to an increase in amounts paid to various consultants and professionals related to our patents, related legal matters and business acquisitions.
 
·
Stock-based compensation expense decreased to $599,000 for the six months ended June 30, 2006 from $2,475,628 for the six months ended June 30, 2005. The decrease in stock-based compensation expense was attributable to the reduction of amortization of deferred compensation.

 
-11-

 
·
For the six months ended June 30, 2006, general and administrative expenses were $361,694 as compared to $168,631 for the six months ended June 30, 2005, an increase of $193,063, or approximately 114.5%. In the 2006 period, we incurred additional marketing fees, travel-related expenses and other administrative expenses due to the acquisition of two pharmaceutical companies, Ze An and Hua Yang.

For the six months ended June 30, 2006, interest expense was $141,918 as compared to $66,703 for the six months ended June 30, 2005 and was related to an increase in borrowings. For the six months ended June 30, 2006, other income was $14,672 as compared to $43,791 for the six months ended June 30, 2005.

As a result of these factors, The Company reported a net loss of $1,111,380 or $0.03 per share for the six months ended June 30, 2006, as compared to a net loss of $2,786,905 or $0.08 per share for the same period in 2005.

Results of Operations for the three months ended June 30, 2006 compared to the three months ended June 30, 2005

Revenues

For the three months ended June 30, 2006, our revenues were $91,312 as compared to $0 for the three months ended June 30 2005, an increase of $91,312. We attribute this increase in net revenues to the Company’s establishment of its drug-screening assay (based on its in vitro cell culture system), and initiated drug screening for anti-HCV therapeutics, to an increased marketing effort, to the gradual acceptance of Shaanxi distribution network and to revenues generated from Hua Yang and Ze An, majority owned subsidiaries the Company acquired on January 19, 2006. The Company was a development stage company prior to June 30, 2005.

Cost of Sales and Gross Profit

For the three months ended June 30, 2006, cost of sales amounted to $78,074 as compared to cost of sales of $0 for the three months ended June 30, 2005. Gross profit for the three months ended June 30, 2006 was $13,238, or 14.5% of revenues, as compared to $0 for the three months ended June 30, 2005.
 
-12-

Operating Expenses

For the three months ended June 30, 2006, total operating expenses were $514,353 as compared to $1,350,307 for the three months ended June 30, 2005, a decrease of $835,954, or approximately 61.9%.

Included in this decrease was:

 
·
For the three months ended June 30, 2006, we incurred selling expense of $34,493 compared to $0 for the three months ended June 30, 2005. The increase was due to an increased marketing effort of Shaanxi and selling activities from Hua Yang and Ze An, majority owned subsidiaries the Company acquired on January 19, 2006.
 
·
For the three months ended June 30, 2006, we incurred research and development expense of $15,036 compared to $0 for the three months ended June 30, 2005, an increase of $15,036.
 
·
For the three months ended June 30, 2006, we incurred professional fees of $21,312 as compared to $38,607 for the three months ended June 30, 2005, a decrease of $17,295, or 44.8%. The decrease was due to a decrease in amounts paid to various consultants and professionals related to our patents and related legal matters.
 
·
Stock-based compensation expense decreased to $249,500 for the three months ended June 30, 2006 from $1,216,106 for the three months ended June 30, 2005. The decrease in stock-based compensation expense was attributable to the reduction of amortization of deferred compensation.
 
·
For the three months ended June 30, 2006, general and administrative expenses were $194,012 as compared to $95,594 for the three months ended June 30, 2005, an increase of $98,418, or approximately 103.0%. In the second quarter of 2006, we incurred additional marketing fees, travel-related expenses and other administrative expenses compared to the same period in the prior year due to the acquisition of two pharmaceutical companies, Ze An and Hua Yang.

For the three months ended June 30, 2006, interest expense was $62,429 as compared to $19,672 for the three months ended June 30, 2005 and was related to an increase in borrowings. For the three months ended June 30, 2006, other income was ($412) as compared to $43,791 for the three months ended June 30, 2005.

As a result of these factors, The Company reported a net loss of $428,071 or $0.01 per share for the three months ended June 30, 2006, as compared to a net loss of $1,326,188 or $0.04 per share for the same period in 2005.

-13-

LIQUIDITY AND CAPITAL RESOURCES
 

At June 30, 2006, we had cash of $89,381.

Net cash used in operating activities for the six months ended June 30, 2006 was $647,551 as compared to net cash used in operating activities of $886,154 for the six months ended June 30, 2005. For the six months ended June 30, 2006, we used cash to fund our loss of $1,111,380 and to fund accounts receivable of $29,540, inventories of $75,042, accounts payable and accrued expenses of $70,631, and other current liabilities of $25,863, increased by minority interests portion of non-majority owned subsidiaries losses, offset by non-cash items such as depreciation and amortization of $192,820, stock-based compensation of $599,000 and decreases in prepayments and other current assets of $8,927. For the six months ended June 30, 2005, we used cash to fund our loss of $2,786,095 and to fund prepayments and other current assets of $695,839. Offsetting these cash outflows were increases in accounts payable of $44,230, non-cash items such as depreciation and amortization of $46,567 and stock-based compensation of $2,475,628, and increases in other current liabilities of $30,165.

Net cash used in investing activities for the six months ended June 30, 2006 was $425,901 as compared to net cash used in investing activities for the six months ended June 30, 2005 of $230,797. For the six months ended June 30, 2006, we used cash of $425,303 for business acquisitions, received cash of $13,784 from business acquisitions, and used cash for capital expenditures of $14,382. For the six months ended June, 2005, we used cash for capital expenditures of $230,797.
Net cash provided by financing activities for the six months ended June 30, 2006 was $1,068,328 as compared to net cash provided by financing activities for the six months ended June 30, 2005 of $289,033. For the six months ended June 30, 2006, the Company received net proceeds of $600,428 from the proceeds of a loan, $425,303 from a stockholder in the form of note payable and $685,544 from stockholders/officers; these were offset by the repayment of mortgages payable of $17,501 and payments on loans payable of $625,446. For the six months ended June 30, 2005, the Company received $363,507 from stockholders/officers, offset by the repayment of mortgages payable of $13,563 and loan payable of $60,911.
 
The Company currently has no material commitments for capital expenditures.
 
We are not aware of any known trends, events or uncertainties that have, or are reasonably likely to have, material impact on the Company’s short-term or long-term liquidity. We have no source of liquidity from operations at the present time. However, we might pursue increasing liquidity through the registration of various shares of stock on a registration statement to be filed with the Securities & Exchange Commission. We are in need of additional funds to meet various anticipated capital expenditures which include research and development for a drug-screening system for anti-HCV drugs and HCV vaccines, production of products for release into the market, mergers of companies that would align the Company’s business plans, and various funds to market our technology and products to create interest in the market place


-14-

There are a number of trends, ventures, and uncertainties that are reasonably expected to have a material impact on the net revenues or income from operations. We will be unable to pursue continued research, development, production, and marketing of our product line in the event the Company is unable to raise sufficient funds to meet these expenses. There is no assurance that we will be able to raise sufficient funds to meet these goals. Further, we are not fully protected in all of our intellectual property rights and failure to do so may allow others to infringe upon the patent.

Currently, the Peoples Republic of China (“PRC”) is in a period of growth and is constantly promoting business development in order to bring more business into China. Additionally, a Chinese corporation can be owned by a United States corporation, however, the laws and regulations of China are subject to change and in the event said change occurs, it may affect the ability of Company to operate in the Peoples Republic of China.

The Company’s future success depends on the continued services of its executive management currently in place. The loss of any of their services could be detrimental to the Company and could have an adverse affect on business development. Future success is also dependent on the ability to identify, hire, train, or retain other qualified employees. Competition for these individuals is intense and increasing.

Going Concern

The report from our independent registered public accounting firm on our audited financial statements at December 31, 2005 contains an explanatory paragraph regarding doubt as to our ability to continue as a going concern. While a significant portion of our net loss for fiscal 2005 is non-cash, we do not presently generate sufficient revenue to fund our operations. The Company's limited financial resources have prevented it from aggressively advertising or developing its product to achieve consumer recognition. In order to sustain our current operations and satisfy our current obligations, as well as to increase sales of our products and services, we will require funds for working capital. The consolidated financial statements do not include any adjustments that might be necessary if the Company is unable to continue as a going concern. Management believes that the actions presently being taken to further implement its business plan and generate revenues provide the opportunity for the Company to continue as a going concern.
 
Off Balance Sheet Arrangements
 
The Company has no off balance sheet arrangements for the period ending June 30, 2006.

-15-

Impact of Recently Issued Accounting Pronouncements

Management does not believe that any other recently issued, but not yet effective accounting pronouncements, if adopted, would have a material effect on the accompanying consolidated financial statements.

Item 3. Controls and Procedures

Our Chief Executive Officer and Chief Financial Officer (collectively, the "Certifying Officers") are responsible for establishing and maintaining disclosure controls and procedures for the Company. Based upon such officers' evaluation of these controls and procedures as of a date as of the end of the period covered by this Quarterly Report, and subject to the limitations noted hereinafter, the Certifying Officers have concluded that our disclosure controls and procedures are effective to ensure that information required to be disclosed by us in this Quarterly Report is accumulated and communicated to management, including our principal executive officers as appropriate, to allow timely decisions regarding required disclosure.

The Certifying Officers have also indicated that there were no significant changes in our internal controls or other factors that could significantly affect such controls subsequent to the date of their evaluation, and there were no corrective actions required with regard to significant deficiencies and material weaknesses.

Our management, including each of the Certifying Officers, does not expect that our disclosure controls or our internal controls will prevent all potential errors and fraud. A control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. In addition, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within a company have been detected. These inherent limitations include the realities that judgments in decision-making can be faulty, and that breakdowns can occur because of simple error or mistake. Additionally, controls can be circumvented by the individual acts of some persons, by collusion of two or more people or by management override of the control. The design of any systems of controls also is based in part upon certain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions. Over time, control may become inadequate because of changes in conditions, or the degree of compliance with the policies or procedures may deteriorate. Because of these inherent limitations in a cost-effective control system, misstatements due to error or fraud may occur and not be detected.
 
-16-

PART II

Item 1. Legal Proceedings


The Company hereby incorporates the disclosures contained in the Form 10-QSB filed for the quarter ended March 31, 2006.
 
 
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

None

Item 3. Defaults upon Senior Securities

None

Item 4. Submission of Matters to a Vote of Security Holders

None

Item 5. Other Information

None
 
-17-

Item 6. Exhibits

The exhibits included in this report are indicated below.

 
-18-

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
     
 
Worldwide Biotech & Pharmaceutical Company
 
 
 
 
 
 
Date:August 1, 2006 By:   /s/ Wenxia Guo
 
Wenxia Guo
 
Chief Executive Officer, Director
(Principal Executive Officer)
     
   
 
 
 
 
 
 
Date:August 1, 2006 By:   /s/ Peiyi Tian
 

Peiyi Tian
VP, Treasurer, CFO, Director
(Principal Financial and Accounting Officer)
     
   
 
 
 
 
 
 
Date:August 1, 2006 By:   /s/ JianJun Liu
 
JianJun Liu
 
Director
     
   
 
 
 
 
 
 
Date:August 1, 2006 By:   /s/ Huimin Zhang
 
Huimin Zhang
 
Director


-19-

 
EX-31.1 2 ex311.htm CERTIFICATION Certification
Exhibit 31.1

 
Rule 13a - 14(a)/15d-14(a) Certification of the Chief Executive Officer 

I, Wenxia Guo, certify that:

1. I have reviewed this Form 10-QSB of Worldwide Biotech & Pharmaceutical Company;

2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the small business issuer as of, and for, the periods presented in this report;

4. The small business issuer’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the small business issuer and have:

(a) designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the small business issuer, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b) evaluated the effectiveness of the small business issuer’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(c) disclosed in this report any change in the small business issuer’s internal control over financial reporting that occurred during the small business issuer’s most recent fiscal quarter (the small business issuer’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the small business issuer’s internal control over financial reporting; and

5. The small business issuer’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the small business issuer’s auditors and the audit committee of the small business issuer’s board of directors (or persons performing the equivalent functions):

(a) all significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the small business issuer’s ability to record, process, summarize and report financial information; and

(b) any fraud, whether or not material, that involves management or other employees who have a significant role in the small business issuer’s internal control over financial reporting.

Date: August 1, 2006

/s/ Wenxia Guo
Wenxia Guo
Chief Executive Officer
 


EX-31.2 3 ex312.htm CERTIFICATION Certification

Exhibit 31.2

 Rule 13a - 14(a)/15d-14(a) Certification of the Chief Financial Officer 

I, Peiyi Tian, certify that:

1. I have reviewed this Form 10-QSB of Worldwide Biotech & Pharmaceutical Company;

2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the small business issuer as of, and for, the periods presented in this report;

4. The small business issuer’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the small business issuer and have:

(a) designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the small business issuer, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b) evaluated the effectiveness of the small business issuer’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(c) disclosed in this report any change in the small business issuer’s internal control over financial reporting that occurred during the small business issuer’s most recent fiscal quarter (the small business issuer’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the small business issuer’s internal control over financial reporting; and

5. The small business issuer’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the small business issuer’s auditors and the audit committee of the small business issuer’s board of directors (or persons performing the equivalent functions):

(a) all significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the small business issuer’s ability to record, process, summarize and report financial information; and

(b) any fraud, whether or not material, that involves management or other employees who have a significant role in the small business issuer’s internal control over financial reporting.

Date: August 1, 2006

/s/ Peiyi Tian
Peiyi Tian
Principal Accounting Officer

 
EX-32.1 4 ex321.htm CERTIFICATION Certification
Exhibit 32.1


CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002


In connection with the Form 10-QSB of Worldwide Biotech & Pharmaceutical Company (the “Company”) on Form 10-QSB for the quarter ending June 30, 2006, as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Wenxia Guo, Chief Executive Officer of the Company, certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that, to the best of my knowledge and belief:

 
(1)
the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and

 
(2)
the information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.




/s/ Wenxia Guo
Wenxia Guo
Chief Executive Officer
August 1, 2006

A signed original of this written statement required by Section 906, or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.

EX-32.2 5 ex322.htm CERTIFICATION Certification

Exhibit 32.2


CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002


In connection with the Form 10-QSB of Worldwide Biotech & Pharmaceutical Company (the “Company”) on Form 10-QSB for the quarter ending June 30, 2006, as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Peiyi Tian , Principal Accounting Officer of the Company, certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that, to the best of my knowledge and belief:

 
(1)
the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and

 
(2)
the information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.




/s/ Peiyi Tian
Peiyi Tian
Principal Accounting Officer
August 1, 2006

A signed original of this written statement required by Section 906, or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.
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