Call Us for any Regulatory Support (ectd, fda, EU, MHRA regulatory authorities): +919998661845
End-to-End Pharmacovigilance Services
We are supporting the entire pharmacovigilance journey
Our Services Include:
1. Pre and Post Marketing ICSR Processing and submission
2. QPPV Service
3. Global Literature Surveillance
4. Signal Management ( Use of both quantitative measures and qualitative analyses )
5. Periodic Safety Reports and Risk Management Plan
6. Draft SDEAs customized as per global regulatory requirements and Review of existing SDEAs
By emphasizing these aspects, NR PharmReg can contribute significantly to the success and reputation of pharmaceutical and CRO clients by ensuring they maintain high standards of quality and compliance.
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