Precise Clinical Trial Documentation

It takes specific expertise, training, and experience to craft the documents that support your clinical trials. Our team of technical medical writers brings flexibility, competency, and consistency to your writing and publishing projects. Not only do we meet your deadlines, but we provide high-quality deliverables in a cost-effective approach.

Services

  • Study protocol writing
  • Clinical trial application writing
  • Clinical study reports writing
  • IMPD writing
  • CER reports
  • Management and writing of region-specific Module 1 documents
  • Scientific manuscripts
  • Support pharmacovigilance in the preparation of RMPs, DSURs, PBRERs, and annual safety reports
  • Writing of Modules 2.5 and 2.7, ISS, ISE, and response documents
  • Publication Management

See how our medical writing team helps you create succinct, compliant documentation.

Get In Touch

Learn how our expert regulatory consultants can help you take your program to the clinic.

Hyderabad, India

403,Vasista Apurva, Green Valley
Road no:3, Banjara Hills
Hyderabad-500034
Phone:- +91 9642288880

Mumbai, India

603, Synergy Business Park, Sahakar Wadi, Off, Aarey Rd, Hanuman Tekdi, Goregaon East, Mumbai-400063 Phone:- +91 9642288880

Newyork, USA

276 Fifth Avenue, Suite 704
Newyork, NY, 10001.
Phone :- 001 (917)-456-9799

Dubai, UAE

#ED008, 5th Floor,
Unit 504-5011, Al Razi Building
P.O.Box: 66566, Dubai, UAE Phone:- +971 559527216

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