Our Medical and Scientific Affairs team renders medical writing, an advisory and monitoring support throughout the development program. We can suggest the most efficient way to design and conduct your development program to maximize success during all phases and offer to develop most effective clinical investigational plan for your clinical trial. Our expert medical writers are very well molded for clinical documentation thus ensures clear, concise and scientifically accurate Clinical Study Protocols, Investigator's Brochure, Clinical Study Report. The clinical documents are thoroughly reviewed by highly qualified team members from relevant departments. Our medical writing team has vast experience in many therapeutic areas including Oncology, Psychiatry, Dermatology, Respiratory Diseases, Endocrinology, Nephrology, Neurology and Cardiology.
The highly experienced team of clinicians and scientists extend their in-depth knowledge to the project management team and investigative sites for medical and scientific queries related to the clinical study.
Development of Protocol, Informed Consent Form (ICF) and Case Report Form (CRF) development
Preparation of Clinical Report, Analytical Report and Statistical Report
Adverse event and concomitant medication reporting using MedDRA and WHO-DD dictionaries
Preparation of FDA Summary Tables for ANDA Submissions
Development of medical investigational reports, regulatory affairs reports
Preparation of annual safety reports, individual case safety reports, Periodic safety update reports
Preparation of preclinical study reports, investigational medicinal product dossiers, toxicology reports, submission of IND and ANDA applications