Services
PHARMACOVIGILENCE
Research with Innovation
Our Clinical Operation team deals with approaching day-to-day as well as strategic business issues systematically and Project management deals with planning, organizing, motivating, and controlling resources to achieve specific goals.
Our clinical trial operations and Project Management team has the experience and know-how needed, your study is supported and optimized to perform at the highest possible level every day.
Developmental
Stage Safety
CT Initiation Support
CT AE/SAE Support
CT Medical Safety
Pre-Authorization Safety
Pharmacovigilance System Master File (PSMF)
Qualified Person responsible for Pharmacovigilance (QPPV)
Risk Management System
Onsite/ Remote Monitoring
Literature Monitoring
Post-Marketing
Data Safety
Medical Information Management System (Call Centre)
Literature Monitoring
Social Media Screening
Data Processing
Post-Marketing Medical Safety
Aggregate Reports (PBRER, PSUR, ACOs, PADER, ASRs, J-PSUR)
Risk Management
Signal Management
Specialized Safety
Support
PV System Support
Integrated QPPV Oversight Office
Labelling Support
Regulatory Support
Affiliate Management
Tactical Project Management
Project Management (PM) Support
Drug Safety Coordination
Repository Management
Tracker Maintenance
Different partnerships
to meet diverse needs
Full Service
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Functional Service
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Consulting
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Case Study
Allergy Clinical Trials: Best Practices and Overview of Recent Asthma and Allergy Research 2021
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Cardiovascular
Infectious Disease
Psychiatry
Dermatology
Nephrology
Respiratory
Request For Proposal
We are offer an array of niche and full-fledged CRO services right from clinical trial protocol development to post-marketing surveillance. Whatever be your need, rope in COD Research experts to breeze through regulatory approvals and get your drug or device on the market soon.
