The medical writing services offered by us encompass the development of Study Protocol (Phase I to Phase IV), Clinical Study Reports (CSR) for Phase I to IV studies, Investigator Brochures (IB), Patient Informed Consent, and Clinical Study Report Synopses.
MIC team comprises of clinical pharmacologist, medical writers and biostatistician. The capabilities and expertise of our team match the highest research standards; and are backed by outstanding academic credentials. In last 2-3 years, we have successfully executed several medical writing and statistical analysis projects on time.
Medical Writing
Development of Study Protocol (Phase I to Phase IV)
Clinical Study Reports (CSR) for Phases I to IV studies
