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Wrong David Vincent?

David W. Vincent

Chief Executive Officer

Validation Technologies , Inc.

HQ Phone:  (800) 930-9222

Direct Phone: (858) ***-****direct phone

Email: d***@***.org

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I agree to the Terms of Service and Privacy Policy. I understand that I will receive a subscription to ZoomInfo Community Edition at no charge in exchange for downloading and installing the ZoomInfo Contact Contributor utility which, among other features, involves sharing my business contacts as well as headers and signature blocks from emails that I receive.

Validation Technologies , Inc.

10815 RANCHO BERNARDO RD

San Diego, California,92127

United States

Company Description

Validation Technologies, Inc. ™ is a leader in the field of Validation Technology services. Our business principal is based on the establishment of long-term relationships with our customers achieved by consistently providing "Value Added" benefit and maintain... more.

Find other employees at this company (99)

Background Information

Employment History

General Manager

VTI Pharmaceutical Technologies Shenzhen Co. Ltd.


Web References(56 Total References)


Leadership | Validation Technologies Incorporated

validation.org [cached]

DAVID W. VINCENT has over thirty-one (31) years' experience in the health care industry specializing in the Biotechnology and pharmaceutical industries.
He has over (20) twenty years dedicated to the field of commissioning and qualification (CQ). He has degrees both in industry microbiology and mechanical engineering technology. He has hands on experience in many areas of Regulatory Affairs, Quality Assurance and Commission/Qualification, Engineering including; regulatory submission preparation, Design Review, Construction Qualification, Project Management, Utility and Process FAT/SAT Commission Plans, and Equipment Qualification implementation. He is especially strong in the areas of Process Development and Validation as well as developing and implementing Environmental Monitoring Programs. Mr. Vincent has spent the last twenty-five (25) years providing validation and quality consultant services to various national and international companies. During this time, he has provided both project management and project execution for numerous national and international clients both national and international. He is responsible for managing and supporting many different product launches. He has written many articles and technical guides on various topics such as Risk Management, Cleaning Validation (Technical Guide), Biological Facility Validation (Technical Guide), Utility System Commissioning and Qualification, etc. He teaches at San Diego State University (SDSU) for their Masters of Regulatory Affairs Degree program in the Field of Validation Technology RA-776.


www.validationworkshop.com

Dr. David W. Vincent
Global Regulatory Consultant Validation Technologies, Inc Dr. Vincent has over thirty-one (32) years' experience in the life science industry specializing in the Pharmaceutical, Biotechnology, and Biopharmaceutical and Medical Device industries. He has spent the last twenty (20) years providing validation and quality consultant services to various companies. He has over (27) twenty-seven years dedicated to the field of commissioning and qualification. He has expertise in many areas of Regulatory Affairs, Quality Assurance and Validation Engineering including; regulatory submission preparation, Design Review, Construction Qualification, Project Management, Utility and Process Equipment Qualification implementation. During this time, Mr. Vincent has provided both project management and project execution for numerous clients national and international. He is responsible for managing and supporting many different product launches and licensing. He is also responsible for implementing and maintaining VTI's Internal Quality Programs, ISO certification and corporate training. Achievements Dr, Vincent is responsible for supporting the regulatory submission and licensing (FDA, EU, WHO) of many facilities both nationally and internationally. He has written many articles and presented national and international on the topics of validation and quality systems. In 2006 because of his year's service in the life science industry he was awarded the businessman of the year for the state of California and the recognition of outstanding meritorious services by the NRCC He is also the co-founder and CEO for Validation Technologies, Inc. USA, VTI Global Regulatory Consultants and VTI Pharmaceutical Technology (Shenzhen) Co. Ltd.


www.validationworkshop.com

Dr. Vincent has over thirty-one (32) years’ experience in the life science industry specializing in the Pharmaceutical, Biotechnology, and Biopharmaceutical and Medical Device industries.
He has spent the last twenty (20) years providing validation and quality consultant services to various companies. He has over (27) twenty-seven years dedicated to the field of commissioning and qualification. He has expertise in many areas of Regulatory Affairs, Quality Assurance and Validation Engineering including; regulatory submission preparation, Design Review, Construction Qualification, Project Management, Utility and Process Equipment Qualification implementation. + Know More Dr. David W. Vincent Global Regulatory Consultant Validation Technologies, Inc TOP REASONS TO ATTEND


Active Product Ingredient: Safety, Transportation, & the United States Economic Gain

www.yourhealthybeing.com [cached]

They are more concerned with their compliance with the FDA to increase their capital gain and supply their own domestic markets. ( David Vincent, CEO/Chairman, Validation Technologies)
The Food and Drug Administration work extremely hard to make sure these overseas manufacturers achieve regulatory compliance. The FDA threatens to stop the production and force recalls. The Food and Drug Administration has enforced many guidelines and principals for these manufacture to meet. The guidelines are established by the FDA are the "Process validation: General Principles and Practices". The compliances of these documents allow manufacturers to produce drugs efficiently and safe, and help these manufacturers cohere to the FDA regulations and requirements. ( David Vincent, CEO/Chairman, Validation Technologies) Furthermore, records of manufacturing must be kept to trace the API batch of origin and to be open for audits. ( David Vincent, CEO/Chairman, Validation Technologies) The Food and Drug Administration reports that only 7 percent of foreign Active Product Ingredient manufactures are inspected, compared to the 97 percent of the United States Active Product Ingredients distributer. ( David Vincent, CEO/Chairman, Validation Technologies) The Food and Drug Administration uses a risk-based approach, meaning inspection are developed and monitored once the drug is on the market, only thirty were inspected in 2007. David Vincent, CEO/Chairman, Validation Technologies


ipacanada.com

David W. Vincent
CEO, Validation Technologies


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