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
to meet diverse needs
Different partnerships
to meet diverse needs
Insights &
Resources
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.
