• Clinical Monitoring
• Regulatory Affairs
• Feasibility and Site Selection
• Site Management
• Project Management
• Pharmacovigilance
• Quality Assurance
• Medical Writing
• Data Management
• Biostatistics
• Patient Recruitment and Retention
• Training and Education

End to End Clinical Trial Management (Feasibilities, Investigator selection, Site selection, Site Monitoring)
Our team expertise ensures that we provide to best end to end management of your clinical trials (Protocol writing – Clinical Study report). Our Experienced monitors provide you the cleanest data from sites with all regulatory and protocol compliances.

Site and Investigator Management

Think-i has strong investigator databases from all Therapeutic areas.
Our customized service for proving investigators and rescue sites from our successful database makes us different from others, we are here providing you what you want

Medical Writing
Think-I with its experienced and proven excellent medical writing team(In house and within the industry), provides a complete solution for your medical writing requirements both, during the clinical phase as well as marketing phase

Clinical Data Management
Our team has experience on several proprietary clinical data management softwares, viz. Oracle Clinical and several other data management softwares.

• Statistical Analysis
• Regulatory Consulting
• Medical Monitoring and Pharmacovigilance