P.G.Program in Medical WritingXcellon Institute
Price on request
- Post Graduate Diploma
This course is designed for individuals who write or review documentation in relevance with Clinical trials and regulatory submissions. Upon completion of the course the individual will be able to have an understanding of what Medical writing encompasses, how to write documents as per the regulatory requirements, write an abstract, manuscript, therapeutic product leaflet. The course will also highlight presentation of Clinical data in an effective and scientific manner.
It covers important aspects of drug development process, medical terminology, Basics of pharmacy, fundamentals of clinical research, clinical pharmacology and therapeutics, epidemiologic principles necessary for designing clinical research studies, Regulatory guidelines and ethics in clinical research, biostatistics, documentation, clinical trial management, Safety monitoring, financial aspects of clinical research, regulatory inspection and basics of medical writing.