cGMP training on 21 CFR part 24 on FDA rules and regulations for combination products

Date : 12th May 2016 to 12th May 2016

Place : United States, New hyde park

Website :https://complianceglobal.us/product/700353/WalterBaker/export-risks-and-risk-mitigation-techniques/1

Contact Person:Compliance Global Inc.

Description:

cGMP training on 21 CFR part 24 on FDA rules and regulations for combination products

cGMP training on 21 CFR part 24 on FDA rules and regulations for combination products will be held in New hyde park,United States on date 2016-05-12

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Deadline for abstracts/proposals : 12th May 2016

Keynote Speakers : David R. Dills, is an independent Global Regulatory Affairs & Compliance Consultant and has an accomplished record with more than 26 years of experience in regulatory affairs, compliance and quality consultative services for early-stage/established Class I/II/III medical devices, IVD's, and bio/pharmaceutical manufacturers on the global landscape. Previously employed, with increasing responsibilities by device manufacturers and consultancies, including a globally recognized CRO, has wo

Conference Highlights :Overview: What is a combination product? What are some examples of combination products? How are combination products assigned for review? Where can I find guidance for how master files can be used in the submission of information relevant to my combination product? Determine which Center will review my combination or non-combination product? Why Should You Attend: These topics and more will be addressed during this Webinar, including FDA rules to codify the GMP requirements, current go

Venue :Compliance Global Inc., 2754 80th Avenue, New Hyde Park, NY 11040, United States

Check the event website for more details.