DIPLOMA IN MEDICAL WRITING AND REGULATORY AFFAIRS

Fineness institute of clinical research

Medical writing refers to the specialized form of writing that focuses on creating scientific and medical documents. It involves communicating complex medical and scientific information in a clear and concise manner, tailored to various audiences, including healthcare professionals, researchers, regulators, and the general public. s. Regulatory affairs refers to the field of expertise that deals with the regulations, policies, and processes related to the development, registration, and commercialization of pharmaceuticals, biologics, medical devices, and other healthcare products.

COURSE CONTENT

  • BASIC TERMINOLOGIES
  • INTRODUCTION TO CLINICAL RESEARCH
  • INTRODUCTION TO MEDICAL WRITING
  • SCIENTIFIC WRITING
  • ICH GUIDELINES
  • MEDICAL WRITING FOR CLINICAL TRIAL
  • MEDICAL WRITING IN POST MARKET PHASE
  • CAREER IN MEDICAL WRITING
  • INTRODUCTION TO REGULATORY AFFAIRS
  • DOCUMENTATION OF DRUG ,MEDICAL DEVICE, BIOLOGICS AND 
  • REGULATORY FILING IN US,EUROPE,INDIA, JAPAN, CANADA AND AUSTRALIA
  • ECTD SUBMISSION
  • INTELLECTUAL  PROPERTY RIGHTS
  • PRIVACY AND CONFIDENTIALITY
  • CAREER IN REGULATORY AFFAIRS
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ATTRACTIVE PRICE AT RS 11,000 FOR LIMITED TIME PERIOD ONLY

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