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With a robust global presence, we provide medical affairs services across diverse therapeutic areas. All our team members have scientific backgrounds, global experience and are entirely up to date with international standards and guidelines.


Our team physicians and clinical research professionals can support the planning, conducting, and evaluating clinical trials, as well as helping with protocol design by advising on study endpoints, eligibility criteria, study assessments, and writing protocol synopsis.

Clinical Concept Development​



Sponsor request for particular service

RFI shared to sponsor

RFP from sponsor

Scope alignment between sponsor & CRO

Budget discussion & finalization

Service awarded to COD

KOM & delegation

Document preparation & service execution

Report preparation & finalization

Regulatory submission & support till approval

Insights &

Request For Proposal

We offer an array of niche and full-fledged CRO services, from clinical trial protocol development to post-marketing surveillance. Whatever your need, rope in COD Research experts to breeze through regulatory approvals and get your drug or device on the market soon.