Dublin, May 19, 2025 (GLOBE NEWSWIRE) -- The "Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Training Course" training has been added to ...

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 ...

(MENAFN- GlobeNewsWire - Nasdaq) Join this comprehensive two-day course to master CMC management for full and generic applications. Enhance your skills in CTD compilation, Module 3 submission, and ...

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 ...

Small and Medium Pharmaceutical Industry Centre (SMPIC) NIPER-SAS Nagar is organising a one-day interactive session for all manufacturers, regulators and suppliers of pharma industry on ‘Common ...

This 3-day workshop will highlight the benefits of the ICH (1) Common Technical Document (CTD) for manufacturers and regulators. Harmonisation of regulatory requirements and high quality of a ...

Regulators at Health Canada have announced the finalization of guidance intended to assist sponsors in preparing electronic common technical documents (eCTDs) to submit their pharmaceutical dossiers ...

(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 ...