•  
  • Home
    • About Us
  • Clinical Trials
    • Pre-Clinical to Clinical Transition Consulting
    • Phase I-IV Project Management
    • Clinical Trials Services
    • Monitoring Services
    • Clinical Study Coordinators
    • Professional Consulting Services
  • Documentation
    • Medical Writing
    • Clinical Trial Documents Translation & QA
    • Additional Medical Language Services
    • Quality Assurance and Compliance
  • Our Clients
    • Medical Devices
    • Biotech
    • Pharmaceuticals
    • Start Up
    • Marketing Clinical Trials
  • Our Advantages
    • Our Advantages
    • Our Company Culture
    • ISO 9001:2008
  • Contact Us
  • Careers
  •  
 
 
Early-Phase Clinical Studies Worldwide
 
Phase II to IV Clinical Studies Management and Monitoring
 
Talk to Us Now!
Our online representatives will be happy to assist you
 

Medical Writing

TransCom's Medical Writing services aim at providing our clients with the best-in-class professionals to meet their goals and objectives.

Our Medical Writers are highly experienced and deeply involved in the Medical Device, Biotechnology and Pharmaceutical industries.

All our Medical Writers sign a project-specific confidentiality agreement.

Our Medical Writing services include: 

Regulatory writing:

  • Investigator Brochure review and/or writing
  • Clinical study protocol and Protocol Summary review and/or writing
  • Interim and Final Clinical study reports
  • Patient Informed Consent (PIC and Patient Information Sheet (PIS)
  • SAE Reports

Educational writing:

  • Sales literature
  • Data presentations
  • Medical journal articles
  • Medical education programs

 

Preparation of Multi-Language Regulatory Documents for Clinical Studies Worldwide
 
Patient Reported Outcome (PRO) Neuropsychological Validation for Clinical Studies
 
Our Clients
Leading CROs, pharmaceutical, medical device and biotech companies

 
Contact Us
 
   Privacy       Terms & Conditions       Disclaimer     

© Copyright 2010 TransCom Global Ltd. All rights reserved.