We take care of your sponsor responsibilities

Empowering Clinical Research

palleos healthcare can take on the Sponsor role, offering a streamlined pathway for a diverse range of clients to conduct clinical trials.

palleos-services-sponsor-services

As your Sponsor, we take full accountability for ensuring compliance with ICH-GCP, ISO 14155, local regulations, and protocol guidelines. Leveraging our expertise as Full-Service CRO, we provide the full spectrum of our services.

Our clients experience liberation from the burden of accountability, reporting, and oversight, enabling them to redirect resources for greater efficiency.

 

Opt for us as your CRO while retaining the Sponsor role, and rest assured that our extensive experience ensures top-notch Sponsor oversight.

Learn more about

Quality Risk Management

One of the most important developments in clinical trial conduct during recent years is the advent of risk-based thinking, introducing a paradigm shift from controlling quality

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Project Management

Any project requires an adequate initiation, planning, controlling and finalization. Specifically clinical research, with its regulatory requirements concerning trial application

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Regulatory Affairs

Approval of relevant study documents by competent authorities and ethic committees is the key requirement for setting up a clinical trial. A concordant positive

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Network

 

„Inspire and being inspired – our network of partners, sites and KOLs makes us ready to meet every challenge.“

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