Course: PG Diploma in Drug Regulatory Affairs
My learning experience in IPM was excellent. Most of the professionals were subject matter expertise. IPM along with knowledge of regulatory affairs, imparts knowledge related to quality control, clinical, intellectual property, quality assurance and manufacturing in API as well as formulation. This helps the candidate to expand their vision in all different branches of Pharmaceutical industry. Also, there are regular updates on regulatory front in pharmaceutical industry to candidate. Thus, they take every initiative to keep their candidate acquainted with upcoming news in regulatory field regarding guidelines.
The notes provided by them are easy to understand and grasp. If any new topic apart from notes is presented in during lectures and candidate is interested in it, they make sure to forward to them.
It is my great pleasure to say something about Ms. Anagha Maharao using this platform. She is thorough with her technical and administrative expertise in regulatory field. Also, one of her specialty is that she never leaves room for the doubts. Which we find in her classroom sessions where she make candidate completely comfortable with subject by taking revision of previous lecture in next lecture before going ahead with any new topic.