We at COD Research believe in providing Clinical trial solutions with a holistic commitment to research. To get those new treatments and therapies, we work to research as efficiently as possible. We work to get the patients for those challenging therapies and we put our commitments and efforts in all requirements of the clinical trial to the desired outcome. Our Team has scientific experts have the experience, ability and expertise to understand and identify key aspects of the clinical trials across therapeutic domains. COD research has offerings of impeccable guidance for seamless project implementation with adherence to regulatory guidelines.

A lot that we DO at COD research is clinical trials.

Our Clinical trial team has therapeutic expertise covering a range of therapeutic areas in lifestyle diseases. We have extensive experience in providing clinical trial solutions for your clinical development programme in the areas of Oncology, Psychiatry, Neurology, Cardiology, Endocrinology Ophthalmology, Dermatology, Orthopedic, Vaccines & Medical Devices. Our team has the capabilities to execute clinical trials with their deep knowledge and scientific guidance. We have the expertise to resolve challenges and bottle necks with respect to trial complexity at critical phases during execution. We are one of the very specialist clinical trial solutions providers where our overall team experience contributes and augments our overall organization expertise since inception.

A perfect complement and match of our scientific team expertise and experience helps us to reach out to clients with supreme confidence and substantiate our vast experience since inception in 2017.

We DELIVER clinical trial solutions in LINE with our experience.

We help you align your safety study plan with complete focus on clinical and safety studies and potential real-world evidence generated e to support value based pricing agreements in your region. We help you blanket cover regulatory compliance, build product recognition and encourage usage with recommendations from health professionals.

Our Global Pharmacovigilance process pathway starts with the building of a safety management plan, safety reporting at site for risk assessment and reporting to relevant regulatory with the collection of the appropriate evidence from the lab reports and related clinical evidence.