RAPS

MHRA Sets No-Deal Brexit Process for Pharma Submissions

Pharmaceutical companies and clinical trial sponsors were directed to follow new guidelines for regulatory submissions that would have to be directly submitted to the UK’s Medicines and Health ...
RAPS

Euro Roundup: MHRA shares guidance on planning approval submissions and seeking support

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has shared guidance on accessing pre-submission advice and support, as well as on providing information about future submissions for ...
Yahoo Finance

Process Validation with Qualification Course: Aligning FDA, EU GMP, MHRA and WHO Standards Across Lifecycle Stages from Design to Continued Verification (ONLINE EVENT: June 3rd ...

Dublin, April 15, 2026 (GLOBE NEWSWIRE)-- The "Process Validation with Qualification (June 3rd - June 4th, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensure your ...
Nasdaq

Athenex Announces UK MHRA Validation of the Marketing Authorization Application for Oral Paclitaxel and Encequidar for Review

BUFFALO, N.Y., Nov. 29, 2021 (GLOBE NEWSWIRE) -- Athenex, Inc., (NASDAQ: ATNX), a global biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies for ...
Mena FN

Process Validation With Qualification Course: Aligning FDA, EU GMP, MHRA And WHO Standards Across Lifecycle Stages From Design To Continued Verification (ONLINE EVENT: June 3Rd ...

(MENAFN- GlobeNewsWire - Nasdaq) Main opportunities include integrating process validation with modern, science-based approaches, utilizing risk-based strategies like QbD, DOE, and PAT, and adhering ...