• Monitors are ready to carry out site qualification visits, site initiation visits, interim monitoring visits, and close-out visits in accordance with the approved protocol.

• Monitors are prepared to prepare and submit the necessary documentation (confirmation letters, follow-up letters, trip reports) as outlined in the clinical monitoring plan (CMP). 

• Monitors comply with the guidelines and regulations set forth by Institutional Review Boards and Regulatory Authorities. 

• Encompasses the review and verification of source documentation, generation and resolution of queries, and ensuring accuracy in safety reporting. 

Various therapeutic areas of expertise are available. 

• Vaccines

• Infectious Disease

• Respiratory 

• Normal Healthy Subjects 

• Neurodegenerative Diseases (CNS)

• Women's Health 

• Oncology

• Ready for both domestic and international travel, we stand prepared to meet the requirements of your global project.