Skip links

We are relentlessly committed to facilitating the clinical development phase of various molecules through our clinical expertise across the therapeutic spectrum, fulfilling your pursuit of bringing new hope and smile to the patients.

Concept compilation based on literature review and development pathway of IND/NDA/505(b)2 molecules for the intended regulatory market in discussion with the sponsor.

● Extensive literature search

● Key enrolment criteria

● Type of studies and its design

● Objectives and endpoints

● Liasoning with KOLs

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

Different models
to meet diverse needs

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.