Investigator Site Feasibility and Selection Database
ISSFD is as a database of qualified, GCP trained and experienced Investigator Site database (tailored to diseases, geographic locations, regulatory inspection history) which offers opportunities to our clinical research clients to speed up their study start-up and maintenance activities by providing potential qualified investigators and investigator sites listings for their clinical studies.
We also offer to Investigator, Investigator Site staff, Ethics Committee and SMOs from our database or newly identified as per client / individual request / proposal – several advanced Good Clinical Practices and Regulatory Trainings such as:
- ICH – GCP Guideline and Indian GCP
- New Drugs and Clinical Trials Rules 2019 India
- USFDA Guidelines
- EMA Guidelines
- Study-specific Training
BEAVER Methodology: Our Investigator Site Feasibility and Selection Database service is basically a six-step systematic, client centric process in order to provide innovative industrious, cost-effective, quality and timely services.
Step 1
Broaden understanding of Investigator and investigator site staff / resources requirements.
Step 2
Evaluate potential unique strategies, risk-based quality approaches for the identification, trainings, and feasibility and selection opportunities.
Step 3
Assess the quality of investigator, site staff, resources, Ethics Committees, SMOs and quality management system.
Step 4
Vow to create and use a metrics that measure investigator sites operational and quality performance, clinical study experiences, subject safety, ethics, regulatory compliance, and overall performance of the study.
Step 5
Engage with Investigator sites, ECs, SMOs, Clients and BEAVER study team and other SMEs time to time
Step 6
Reinforce your interest in a company and the clinical research position you’re applying for by consistently and persistently following up with the right decision makers