Medical Writing, Medical Writing in Clinical Research, Medico-marketing in Clinical Trials.

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:

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

We are happy to note that the services offered by Samhitha Research organisation is prompt and timely. Their approach is professional , customer friendly . The service is exemplary ,quick and prompt. Staff are easily reachable and ready to help any time of the hour. Wish them all the best in thier future endeavours.

Dr.Sanjeev B Rai

Chief of Research, Father Muller Medical College and Hospital, Mangalore

We have been in business with samahitha since 2 yrs. I personally wanted to share a quick note that I am glad about our association with samahitha. They have their Network across India with a good knowledge staff. We would like to have our association with you in future also.

Dr.Chandrashekar K

Project Manager, Croissance Clinical Research