Regulatory & Medical Writing
Regulatory & Medical Writing
We Deliver The Best

Being one among the critical points in completion of a Clinical trial, the medical writing directly impacts on the success or failure of any product/device. Accuracy, precision and adhering to timelines being the major factors expected by the Regulatory bodies, delay in this stage causes delay in profit actualization in terms of subject benefits as well as return on investments.

Our team of experienced Medical writers provides you services like:

  1. ● Assist in study design and protocol development
  2. ● Assistance in preparation of study documents
  3. ● Assistance regarding the Common technical document
  4. ● Clinical Study Report preparation
  5. ● Preparation of dossiers to regulatory submission
  6. ● Responses to Regulatory Authorities, comment letters and assessment reports
  7. ● Consultancy for Regulatory submission
  8. ● Import/ Export licensing support
  9. ● Medico-marketing
  10. ● Regulatory labeling and artwork