Effective site management is crucial for the success of clinical trials. It ensures that site teams conduct trials efficiently, adhering to protocols, Good Clinical Practice (GCP) standards, and relevant regulations. This approach is essential for maintaining data accuracy and safeguarding participants.

Feasibility Assessments

Protocol Development

Site and Investigator Selection

Regulatory Compliance

Protocol Development

Your Partner in Developing Robust Clinical Trial Protocols

At Yayasan RPRI, we understand that a meticulously crafted protocol is the cornerstone of successful clinical research. Our protocol development service is designed to guide investigators and sponsors through the intricate process of creating comprehensive, scientifically rigorous, and regulatory-compliant protocols.

Project Implementation

Project Implementation at RPRI: Partnering for Progress

Effective project implementation in healthcare requires adequate resources, expertise, and experience. Many organizations struggle with selecting the right methodologies due to limited references.

Take Action, No Discrimination!

Harnessing social media to deliver health education and promotion for community & make community engagement for eradicating Tuberculosis.

Tuberculosis TV

Unlocking an Indonesia free of TB and respiratory problems