Clintegral is a Contract Monitoring Organization which provides clinical trial monitoring services for phase II, III and IV studies in India. We are committed to provide Customized and Quality Monitoring Services (CQMS) by identifying and incorporating customer core needs in basic  monitoring system as elaborated in GCP and Indian governing laws (Schedule Y, Drugs and Cosmetics Rule, 1945). CQMS utilizes a team structure of highly skilled clinical research professionals based in New Delhi, India. The flexifit nature of our team is able to encompass Phase II-IV studies, therapeutic area ranging from:

Neurology
Endocrinology
Neuropathy
Pediatrics
Vaccines
Antibiotics
And many more...

Deploy us as if it is your Integral system
We strive to deliver beyond your expectations

Clintegral is one of its kind organization which enables you to own a monitoring team in India, unlike other conventional CROs; and fulfill your drug development needs in a strategic way.

Our working model allows you to virtually own clinical trial monitoring team in India for a specified period which comprises of a highly skilled clinical research professionals (centralized) trained to provide customized deliverables in timely manner.

The model also allows you to cut down your development cost by nearly 30%, as we adopt a pass-thorugh costing technique. This technique gives you a better control over the monitoring budget utilisation right from the start of the study owing to its transparency. For more details on this costing technique, please email us at info@clintegral.com

At Clintegral, we provide incomparable research services to match your specific clinical requirements by focusing on three performance drivers of monitoring and trial management services.

Customization
Quality
Effective implementation

We start by identifying your needs and customize our monitoring and reporting systems accordingly. All of our Clinical Monitors are professionals with several years of field experience, GCP/ICH training and an attitude towards continuous quality improvement. Our clinical monitors typically have over 2 years of field experience and typically come from a background in medical, pharmaceutical sciences and advanced degrees in Life Science related areas of study. Clintegral will systematically match monitors with the most relevant therapeutic area and disease site expertise for your study.

We listen first. Talk and make us to work your way

If you would like more information about Clintegral, services offered, costing techinique adopted and how Clintegral can start providing one of the best managed and experienced monitoring services for your company, plesae email us at info@clintegral.com

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