Clinical Data Collection
Our clinical data collection services are designed to gather comprehensive and reliable data for regulatory submissions. We manage the entire process from planning clinical investigations to obtaining necessary approvals and conducting clinical studies.
- Clinical Investigation planning
We develop detailed plans for clinical investigations, outlining study objectives, methodologies, and timelines to ensure compliance with regulatory requirements and data integrity.
- Compilation of all Essential Documents
Our team compiles and organizes all required documentation, including protocols, investigator brochures, and informed consent forms, to support clinical investigations and meet regulatory standards.
- Conducting Feasibility studies
We conduct feasibility studies to assess the practicality and potential success of clinical investigations, helping you identify potential challenges and optimize study designs.
- Obtaining Clinical Investigation Regulatory approvals
We manage the submission process for clinical investigation applications, ensuring all necessary approvals are obtained from regulatory authorities and ethics committees.
- Conducting the clinical studies
Our experts oversee the execution of clinical studies, ensuring adherence to the approved protocols and compliance with Good Clinical Practice (GCP) standards.