Our service area also includes investigation and development of drug molecules and medical devices. In clinical trials area, we are involved in the management of early to late phase studies including the evaluation of the data (feasibility, protocol writing, Ethics Committee and Ministry of Health dossier preparation and submission, adverse event notification, data collection, analysis and reporting) of these clinical trials. Following the investigation of drug molecules and medical devices, Istanbul Consulting Group provides guidance at the next level with the management of clinical trials process in compliance with national legislation and international standards at a very rapid and high quality level, Istanbul Consulting Group reduces the timeframe that a drug is being marketed to an optimal level.