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The Business of Contracting with Clinical Trial Sites - Hogan Lovells

The Business of Contracting with Clinical Trial Sites - Hogan Lovells 2025

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The document discusses the complexities of clinical trial agreements from the sponsor's perspective, focusing on key issues such as confidentiality, intellectual property (IP), and publication rights. It highlights the challenges sponsors face in negotiating these agreements with institutions and principal investigators (PIs), particularly regarding the definition of confidential information and the ownership of IP developed during trials. The article emphasizes the need for clear communication and compromise between sponsors and institutions to protect both parties' interests while facilitating research.

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What is the best website to find clinical trials?

Sponsor: Third Party Selection and Management A vendor (or Service Provider under ICH E6R3) is a person or organization (commercial, academic, or other) providing a service to either the sponsor or the investigator to fulfil one or more of their trial-related activities.

What is a CTA in clinical trials?

The principal investigator (PI) is the person responsible for all aspects of the study at the research site. The PI is usually a medical doctor.

Who is responsible for the conduct of the clinical trial at a trial site?

Around the Nation and Worldwide NIH conducts clinical research trials for many diseases and conditions, including cancer , Alzheimers disease , allergy and infectious diseases , and neurological disorders . To search for other diseases and conditions, you can visit ClinicalTrials.gov.

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