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Technology Transfer and Validation for Medical Devices and Pharmaceuticals: The Link between Development, Validation and Commercial Production
The parallel requirements for medical devices and pharmaceuticals are incorporated into this comprehensive webinar that delineates the foundation for technology transfer and validation, encompassing regulatory requirements and voluntary guidance.
Why Should You Attend:
This webinar will discuss the concepts of technology transfer and validation as they relate to the commercial production of medical devices and pharmaceuticals. Research and development (R&D) activities are not regulated; however, the outputs from R&D serve as the launching pad for the manufacturing processes.
Who Will Benefit:
This webinar will be of interest to professionals in early or middle phase in their careers in research and development, product development, manufacturing or validation in the pharmaceutical or medical device industries. Professionals interested in a refresher course on the concepts of technology transfer and validation will also benefit. Participants will include:
Carlos A. Rodriguez-Garcia, PhD, ASQ CSSGB, CBA, is president of BioMed Pharma Consulting, LLC, an independent consulting firm providing services in quality management systems to the pharmaceutical and medical device industries. Mr. Rodriguez-Garcia has over 18 years of experience in the regulated industry, the vast majority in quality management, encompassing a wide scope of products and processes in medical devices and pharmaceuticals: plastics, parenterals and aseptic processes.
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.
If the Technology Transfer and Validation for Medical Devices and Pharmaceuticals: The Link between Development, Validation and Commercial Production is important to your business, act now and make the appropriate connections. See the contact information below.
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