Clinical Research Organisation (CRO)

With its unparalleled experience of managing hundreds of studies as a Site Development and Management Organisation (SDMO) and as a Specialized Contract Research Organization (SCRO), IDD has evolved further and established a full-fledged Contract Research Organization (CRO) as an independent division to offer Clinical Research solutions to its Clients in the Pharmaceutical, Nutraceutical, Biotechnology and Medical Device industry. The CRO supports their Clients in the conduct of Clinical Trials, which includes Pilot Studies, Pivotal Studies, Phase Studies and Therapeutic Equivalence studies, right from designing the study till reporting the same.

iDD’s CRO was established with an aim to build a full-fledge CRO offering end to end service with respect to phase studies, with systems and processes in compliance with global regulatory standards ( including ICH-GCP, ICMR, EMEA and FDA Standards). iDD with the back-up of its extended working experience with many renowned global pharmaceutical companies as a SDMO and also in various indications starting from infectious disease to Oncology, is committed to offer the best service with respect to study design, management, conduct and reporting.

Considering the advantage having one of the well-established networks of investigators through the SDMO division and customised systems and resources to handle multi center long term PMS studies with huge patient pool through SCRO division; iDD CRO will be able to give you most cost effective, highly compliant and timely service.

Services

• Regulatory Affairs
• Clinical Operations
• Quality Assurance
• Clinical Data Management
• Biostatistics
• Pharmacovigilance
• Medical Writing
• Project Management

Company Highlights

• Having an unparalleled experience of handling hundreds of studies as SDMO
• Having an experience of handling hundreds of PMS studies as SCRO
• Having an experience of simultaneously handling several sites with around hundred active projects
• Ability to conduct Phase I to Phase IV studies, Investigator Initiated Trials (IITs), Medico Marketing Studies (MMSs), Post Marketing Surveillance Studies (PMSS) and Therapeutic equivalence studies
• Full time experienced Clinical Research Coordinators across sites in India, to have complete control over the site
• Well accepted by all clients as one of the most cost effective and quality assured CRO
• Worked with many renowned global pharmaceutical companies
• Had developed a customized system to handle small budget studies without compromising the quality