North Chapter of ISCR is pleased to announce a virtual workshop on Clinical Trial Liability, Indemnity and Compensation scheduled on 24th September 2022, 10.30 onwards.
Highlights: The clinical trial liability and indemnity is one of the important aspects of clinical trial documents in clinical research. The seminar will address the various concerns involved in clinical trial liability & Indemnity as both are very critical elements of clinical research process and important to understand in order to have proper risk management measures in place for Clinical Trials. After the implementation of “New drug and clinical trial Rule-2019” minimum compensation has been defined for the clinical trial participant in case of injury. But still many questions need to be addressed in order to have proper risk management measures in place for Clinical Trials. There are many questions related to insurance of clinical trial that keep bustling in the minds of Principal Investigator and other stakeholders. This seminar will address the various concerns involved in clinical trial liability, Indemnity and compensation such as;
What is Clinical Trial Liability & Indemnity?
How much insurance is sufficient?
Where to get insurance for clinical trial in India?
What are the differences in various countries?
What are the hurdles in claim settlement?
Key things to understand in an insurance policy for clinical trial?
Which insurance or indemnity work for academic clinical trial?
This interactive session will help to understand how to minimize financial risk (owing to participants injury) of clinical trial through well curated insurance policy. It will also highlight important issues or hurdles related to claim settlement in case of any injury. The intended audience includes PI, patients, sponsors, students, CRO, insurer, brokers and any participants in clinical trials. At the end of the workshop the participants should understand the insurance policy document, claim settlement procedure and check list of documents for claim settlement in the ever-changing- environment of regulations.
Who should attend: Clinicians, trial managers, EC members and anyone who is involved in execution of clinical trial. This workshop is also open to scientific writers, regulatory affairs specialists, clinical trial investigators, research scholars, scientists, and health care professionals from pharmaceutical industry, contract research organizations, government agencies, non-profit organizations/associations, and academia, medical, pharmacy or life-science students or professionals interested in making a career in clinical research.
Registration fees: Rs. 500/-