Dublin, Nov. 14, 2025 (GLOBE NEWSWIRE) -- The "The Common Technical Document (CTD) Submission in the MENA Region Training Course (Nov 28, 2025)" training has been added to ResearchAndMarkets.com's ...

Drug approval is the goal of the long process of drug development. Once preclinical and clinical trial data have been collected, a New Drug Application must be submitted to the regulatory authority ...

Dublin, Feb. 24, 2025 (GLOBE NEWSWIRE) -- The "The Common Technical Document Training Course" conference has been added to ResearchAndMarkets.com's offering. This interactive two-day course will ...

This interactive two-day course will provide you with a clear and comprehensive understanding of the regulatory and technical requirements for CMC management of your full and generic application in ...

(MENAFN- GlobeNewsWire - Nasdaq) Opportunity exists to enhance understanding of technical and regulatory CTD requirements for generic submissions in MENA, addressing complexities, and learning from US ...