Dublin, June 27, 2024 (GLOBE NEWSWIRE) -- The "eCTD Submissions - Fundamentals and Process" training has been added to ResearchAndMarkets.com's offering. eCTD Submissions, or electronic Common ...
Dublin, May 19, 2025 (GLOBE NEWSWIRE) -- The "Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Training Course" training has been added to ...
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 ...
(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 ...
With an approaching deadline of 1 January 2019, Health Canada is requesting industry input on establishing mandatory requirements for submitting drug master files (DMFs) using the electronic common ...
(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 ...
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 ...
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 ...
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