IRB/IEC Review Services

IRB/IECs is the consortium constituted to review and monitor the biomedical research involving human subjects. IRB/IEC consortium plays an important role in protecting and safe guard the rights and welfare of the human participants in the biomedical research. Protocol approval from IRB/IEC is an initial step to begin the clinical trials. Being a clinical trial service provider, we know how to guide the sponsor towards IRB/IEC approval and making the way to forward. Presenting the research proposal and responses to the queries raised by the IRB/IEC consortium is an important aspect to get the approval and we have huge experience in handling review board requirements since from submission of protocol package to the final approval.

In clinical trials coordination and timelines are important to finish the project in committed period so, we are the catalyst to navigate your trial with fastrack IRB/IEC approvals. Our team has thorough knowledge and expertise on various ethical aspects human populations involving in clinical trial which includes ICH GCP, WHO GCP, NDCT 2019 CDSCO, NABH, ICMR guidance

Identification of IRB or IEC based on the site

Identification of IRB or IEC based on the site

Submission of Protocol Package to the IRB/IEC

Support in Handling of AE/SAEs

Fastrack the Approval Process

Support in Notifications, Amendments, Version changes

Response to the Queries & address COI if any

Final Approved Copies to navigate the Trial

Handling all the IEC/IRBs in single platform

Support in Periodic Reporting

Dedicated person for handling IRB/IEC activities