Pharmaceutical Classroom Training

"Knowledge transfer is a basic mechanism of learning "

  • Overview of Worldwide Regulatory Bodies
  • Registration Procedure for USFDA, EMA and RoW
  • Organization of CTD

Regulatory systems of USFDA, Europe, Health Canada, UK-MHRA, MCC, TGA, MHLW, Indian CDSCO, DCGI, RoW etc.



The following topics are essential for many departments in the industry –

  • How to improve Technical writing/Review skills?
  • What are the International Document Standards?
  • Basics of CMC(Chemistry, Mfg, Control)
  • How to write PDR as per ICH-Q-8?

We cover many such practical topics that find utility in industry channels and day-to-day working environment of the corporate offices. These courses will equip both students and professionals with practical knowledge and enrich them with technical expertise that will help them be more productive and resourceful in their respective roles and responsibilities.