Thorough Clinical Monitoring Proswell guarantees study integrity, protocol compliance, patient safety, and accurate data collection. All our clinical monitors are our full-time employees with experience in different therapeutic indications and regional availability in variety of China Mainland cities. Proswell uses technological advances to support monitoring activities and to meet our client clinical trial need.

• Site Qualification and Initiation

• Management/Facilitation of IRB/EC submissions

• Monitoring Plan and Study Documents Development

• Regulatory Compliance Monitoring

• Risk-based Clinical Monitoring

• Monitoring Report Development

• Set up and Maintain eTMF

• Manage & Collect Regulatory Documents

• Adverse event Follow Up