An accurate feasibility assessment plays a crucial role in identifying and assessing status of the clinical study. We provide assistance in deciding whether to proceed with, alter, or drop a particular project or plan of action.
We have a extreme knowledge of the strengths and weaknesses of the clinical trial process within each site and are well placed to make thorough assessments of the suitability for a particular study. We respond within a week of conducting the assessment. The outstanding results help us in creating trust and confidence within our clients. Give us the opportunity to work for you; we will let you know the challenges, trends and issues to save your time, money and stress.
Investigator Identification: We can quickly shortlist investigators across a range of parameters including investigator qualification, specializations, clinical trial experience, recruitment records and thus help in placing your study in experienced hands.
Site Identification: For successful implementation of trial studies it is important to identify proper sites and we help pharmaceutical companies in the identification of potential, ICH-GCP compliant sites.
At IICRM, we offer free feasibility assessment. To request your feasibility assessment, Site Preparation and Up gradation : Our perpetual efforts to upgrade infrastructure at sites is in accordance with the protocol specific requirement making sure they qualify for participating in the trial.
IRB / IEC Submissions We understand the ethics and regulatory environment in India better with our rich experience in handling large number of studies across various centers in India. We work closely with Investigators ensuring one time submission & approval with all subsequent amendments are conveyed and favorable approval obtained. All safety events are reported within the specified timelines with timely reporting on the progress of the study.
