Common Technical Document News Today

Join us for the WHO's Week of Quality for IVDs training program. Register your interest to participate in this valuable training program. IVD manufacturers and regulatory authorities (Ministry of Health, National Regulatory Authorities) in all WHO regions are welcome to attend.

Join us for the WHO's Week of Quality for IVDs training program. Register your interest to participate in this valuable training program. IVD manufacturers and regulatory authorities (Ministry of Health, National Regulatory Authorities) in all WHO regions are welcome to attend.

Dublin, May 22, 2023 (GLOBE NEWSWIRE) -- The "The FDA (Food and Drug Administration) Drug Approval Process Training Course" conference has been added to ...

/PRNewswire/ -- The "The FDA (Food and Drug Administration) Drug Approval Process Training Course" conference has been added to ResearchAndMarkets.coms...

The European Union (EU) has just published its proposals to revise its general pharmaceutical legislation. One of the objectives of the revision is to reduce the regulatory burden on...

/PRNewswire/ -- The "EU (European Union) Pharmaceutical Regulations & Strategy Training Course" conference has been added to ResearchAndMarkets.coms offering....

/PRNewswire/ -- The "Development of Combination Products: Critical Interactions Training Course" conference has been added to ResearchAndMarkets.coms offering....

The "Development of Combination Products: Critical Interactions Training Course" conference has been added to ResearchAndMarkets.com's offering. Drug/device and device/drug combination products are

How to apply for marketing authorisation via this new procedure.

/PRNewswire/ -- The "Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Training Course" conference has been added...