Megapharm has an in-house Regulatory Department carrying out all registration procedures for new chemical entities, renewals, pharmacovigilance, cold chain management etc.
Our Regulatory Department operates according to our strict Standard Operational Procedure (SOP) to comply with local and global regulatory procedures and standards.
Megapharm has successfully submitted more than 100 Marketing Authorization Applications in different segments including New Chemical entities, biological products, medical devices, and food for special medicinal purposes (FSMP).
Our Regulatory Department covers the following aspects:
- New product submission for Marketing Authorization (MA)
- Renewals, updates, and variations
- Quality system – GMP Approved
- Batch Release – Q.P.
- Medical Nutrition Regulatory Affairs
September 19, 2023