PV & Drug Safety
Post- marketing PHARMACOVIGILENCE
QPPV/Responsible Person Services
ICSR management, being the most scientific and priory activities, needs multiple platforms trained team. COD provides complete ICSR management services via in-house/client hosting system.
As case processing is dynamic and resource driven, we do consider supporting client on all the following aspects:
Case Intake and Processing Services
Scheduling
Authoring
SME Review
Submission
Specialized Aggregate Reports Services
Submission of RFI and PRAC assessment Report
Line listings Review
Regulatory Website review & tracking of PSUR report
Publishing of Report
MAH System Support
GAP Analysis/Audit
Oversight System Setup
Workshop/Training
Procedure Development
QPPV/PV System Master File
ICSR management, being the most scientific and priory activities, needs multiple platforms trained team. COD provides complete ICSR management services via in-house/client hosting system.
As case processing is dynamic and resource driven, we do consider supporting client on all the following aspects:
Case Intake and Processing Services
Scheduling
Authoring
SME Review
Submission
Specialized Aggregate Reports Services
Submission of RFI and PRAC assessment Report
Line listings Review
Regulatory Website review & tracking of PSUR report
Publishing of Report
MAH System Support
GAP Analysis/Audit
Oversight System Setup
Workshop/Training
Procedure Development
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Literature Monitoring[hfe_template id='2091']
Case Processing
ICSR management, being the most scientific and priory activities, needs multiple platforms trained team. COD provides complete ICSR management services via in-house/client hosting system.
As case processing is dynamic and resource driven, we do consider supporting client on all the following aspects:
Case Intake and Processing Services
Scheduling
Authoring
SME Review
Submission
Specialized Aggregate Reports Services
Submission of RFI and PRAC assessment Report
Line listings Review
Regulatory Website review & tracking of PSUR report
Publishing of Report
MAH System Support
GAP Analysis/Audit
Oversight System Setup
Workshop/Training
Procedure Development
Aggregate Reports[hfe_template id='2091']
Risk Management Systems[hfe_template id='2091']
Signal Management[hfe_template id='2091']
Alliance Partner Management[hfe_template id='2091']
Tactical Project Management[hfe_template id='2091']
Regulatory Portal Management[hfe_template id='2091']
Case Study
Allergy Clinical Trials: Best Practices and Overview of Recent Asthma and Allergy Research 2021
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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.
