Tag : InPerson

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2-Day In-Person Seminar: Medical Device Single Audit Program Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Newsemia
Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite...
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Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs): One and a Half day In-Person Seminar – ResearchAndMarkets.com

Newsemia
DUBLIN–(BUSINESS WIRE)–The “Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs): One and a Half day In-Person Seminar” conference has been added to ResearchAndMarkets.com’s offering....

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