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.
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
to meet diverse needs
Different partnerships
to meet diverse needs
Insights &
Resources
Strategic Planning for Patient Recruitment
Nov 01, 2021
BlogRegulatory Pathways for Vaccine Development and its use in the Current Scenario of COVID-19
Jun 25, 2021
BlogMultiple Indication in Oncology
May 15, 2021
BlogRequest 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.