Medical Writing for Essential Clinical Trial Documents
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Medical Writing for Essential Clinical Trial Documents

Medical Writing for Essential Clinical Trial Documents


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International Edition


About the Book

The book covers training on scientific writing of essential clinical trial documents which includes Protocol, Standard Operation Procedures, Informed Consent Document, Case Report Forms, Data Validation Plan, Clinical Study Report, Publication etc.
About the Author: With the accomplishment of PhD and Masters in Pharmacy, Dr T C George has been engaged in clinical trial operations for more than 12 years. He has been a part of more than 100 clinical trials on various positions. He started his career as Clinical Trial Coordinator and then appraised to as Clinical Trial Monitor in a short span of time. For a long time he worked as a freelancer for various Sponsor and CROs as a Clinical Trial Monitor. Presently he is working as Project Manager and working on various therapeutic areas of clinical studies. He has won several awards and recognition for his work and dedication. To uplift the clinical research community, he has participated in various domestic and international forums & discussion to share his experience and knowledge.


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Product Details
  • ISBN-13: 9781511451437
  • Publisher: Createspace Independent Publishing Platform
  • Publisher Imprint: Createspace Independent Publishing Platform
  • Height: 254 mm
  • No of Pages: 128
  • Series Title: English
  • Sub Title: A training manual to learn & create clinical trial documents
  • Width: 178 mm
  • ISBN-10: 1511451432
  • Publisher Date: 25 Mar 2015
  • Binding: Paperback
  • Language: English
  • Returnable: N
  • Spine Width: 7 mm
  • Weight: 286 gr


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