CARE commits to provide Sponsors with the highly knowledgeable clinical research professionals for on-time and efficient execution of projects.
CARE clinical research provides comprehensive site management and monitoring activities to include the following types of monitoring visits:

• Feasibility study
• Site Identification
• Pre study evaluation visits
• Regulatory submissions
• Ethics committee submissions
• Initiation visits
• Interim monitoring visits
• Close out visits

All activities are performed in accordance with ICH-GCP guidelines to ensure all the investigational sites are compliant with all applicable regulations and protocol requirements.

CARE always ensure and emphasize on the best clinical services, highest ethical standard and quality clinical data.