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Enhancing Safety Monitoring with Literature & ICSR Integration
Our expertise in Individual Case Safety Reports (ICSR) and Pharmacovigilance Case Processing ensures that your clinical trials and post-marketing surveillance are conducted with the highest standards of safety and efficacy.
102350+ ICSRs processed
COD hosted PV Database & all renowned Safety Database Trained team
AI driven Automated Literature screening tool
187480+ Literature Articles screened
ICSR Support
Case Intake & Processing Services
- EV WEB Downloading
- Case Intake and Booking
- Triaging of Cases
- Data Entry of ICSRs
- Peer review & QC of ICSRs
- Physician Review/Medical Review of ICSRs
Automated Literature Screening
At COD, we understand the crucial significance of pharmacovigilance in safeguarding patient’s health. Our wide-ranging Literature Screening Pharmacovigilance services are designed to meticulously monitor and analyze scientific literature to identify potential adverse drug reactions (ADRs) and ensure compliance with global regulatory requirements. We also identify any merging safety concerns being discussed in literature.
We can assist you with monitoring the safety of your products via screening of worldwide and local scientific & medical published and unplublished literatures.
- Systematically reviewing scientific publications to detect new safety signals
- Global literature screening
- Proficiency in managing screening throughs Embase, PubMed, and customer-specified databases
- Medical Literature Monitoring (MLM) for EU
- Full text article Procurement and Copyright Management
- Translation management
- Local literature screening for EU & non_EU countries
Request for Proposal
COD is dedicated to strengthening our pharmacovigilance capabilities and drug safety through partnerships that reinforce our commitment to patient safety and regulatory compliance. We eagerly anticipate collaborating with you and supporting your needs in Global ICSR Submission and literature monitoring.