Post Graduate Diploma in Medical Writing
Medical Writing is one of those activities where, Changing market dynamics, expiring patents, and depleted product pipelines are all exerting pressure on pharmaceutical companies to outsource non-core activities in an effort to control costs and enhance drug-development cycle time. Medical Writing – an area that, although not at the core of pharmaceutical operations, has become increasingly critical as regulatory agencies have adopted more elaborate review measures that require substantial amounts of documentation.
Medical writing involves creating well-structured scientific documents that include clinical research documents, content for healthcare websites, health magazines, journals and news.
The Post Graduate Diploma in Medical Writing has been perfectly structured by expert faculties of JCL themselves and thus comprehensive coverage and understanding of the industry and its functional areas is promised. The Offline & Online live interactive course has its own advantages which are definite to benefit one to all participants. We targets to teach, train and polish aspirants in Medical Writing with clear understanding and complete knowledge of this industry and its working.
Eligibility: Post Graduate candidates in Life science/ Medical/ Pharma/ MBBS/ BDS/ BHS/ BUMS/ BAMS etc.
Duration: 3 Months
Placement: 100% placement assistance
Course Curriculum:
Module 1: Introduction to Medical Writing (Types and Requirements)
Module 2: Writer’s Role -Need or Basis of Medical Writing
Module 3: Tools Used for Medical Writing- Reference, Writing Style and Resources
Module 4: Medical Writing for Clinical Research Industry (Designing and Preparation of Protocols, ICDs, CRFs etc)
Module 5: Writing for Regulatory submissions and Drug Promotion Activities (IND, NDA, BLA, SNDA, ANDA)
Module 6: Dossier preparation in CTD Format, eCTD Submissions
Module 7: Scientific Writing (Manuscript, Abstract writing, review articles)
Module 8: Documents in Medico Marketing
Module 9: Achieving Flow and Cohesiveness
Module 10: Managing the Review Process (Quality Control Check/Proof Reading Concept)
Module 11: Judicial/ Copyright Issues in Medical Writing & Unethical Practice
Module 12: Ethics and Ethical Guidelines for Clinical Trials and Good Clinical Practice (GCP)
Module 13 -Clinical Trials -Latest updates: New Drugs and Clinical Trials Rules, 2019
Module 14: Industry Based Case Studies
Other benefits:
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- Digital Notes
- Industry Based Learning
- Faculty with 20+ years of Clinical research Industry Experience
- Live Interactive Sessions
- Limited Seats Batch
- 100% placement assistance
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