Our Services

Feasibility Assessment

Developing strategies to address potential costs and risks associated with proposed trials.

Regulatory Compliance

Monitoring adherence to protocols, ICH-GCP standards, and relevant regulations to ensure timely and compliant trial execution.

Protocol Development

Evaluating and choosing sites and investigators to ensure they meet the trial’s requirements.

Site and Investigator Selection

Our SMO division provides a wide array of services to support clinical trials, including:

Developing robust research protocol is essential to ensure the successful conduct of every clinical trials.

Our Supports

Assisting sites in achieving target recruitment numbers and meeting deadlines.

Expert Study Staff

Providing dedicated and proficient personnel to ensure trials are conducted according to GCP guidelines.

Strengthening site capabilities through the development of Clinical Research Units.

Delivering thorough training for study staff to uphold high standards in clinical research.

Furthermore, our SMO division supports clinical trial sites with:

Capability Enhancement

Training Initiatives

Patient Recruitment