Training to the site:

We provide the onsite training to the Investigator and staff regarding
• Working with/interacting with Institutional Review Boards.
• Understanding and complying with regulatory authorities.
• Effective subject consent processes.
• Ethics/Protection of human subjects.
• Maintaining good standards.
• Regulatory document preparation and maintenance
 

Training to CRC
We are having experienced research team which are fully dedicated to train the clinical research coordinators on the following topics.
• Overview of drug development
• Clinical trial process
• ICH-GCP guidelines
• Informed consent documentation
• Essential clinical trial documents
• Clinical trial monitoring
• Data management
• Team exercises