MC Pharma

12/05/2026

10/05/2026

18/03/2026

We’re excited to announce that MC Pharma will be exhibiting at SAPHEX 2026!

Make sure to stop by Stand A15 and say hello.
See you soon!

26/12/2025

International Dossier Evaluation is the systematic, evidence-based appraisal of a Common Technical Document (CTD/eCTD) by national regulatory authorities (NRAs) to confirm the safety, efficacy and quality of a health product before approval. Harmonised guidelines from the ICH, EMA, FDA, WHO and SAHPRA increasingly promote work-sharing, reliance and electronic formats, allowing well-prepared dossiers to move faster across borders.

This article explains the principles, benefits and challenges of international dossier review and shows how MC Pharma’s regulatory team helps sponsors navigate each stage from technical gap analysis to post-approval life-cycle management.

Explore SAHPRA reliance pathways, AMA harmonisation and MC Pharma’s end-to-end regulatory services.

25/12/2025

Merry Christmas from MC Pharma!
Wishing you and your loved ones a joyful festive season filled with peace, happiness, and unforgettable moments.
Thank you for being part of our journey this year—we look forward to an amazing 2026 together!
Stay safe, stay blessed, and enjoy the magic of Christmas!