Global Pharmacovigilance Services for Scalable Regulatory Compliance
Absolute Regulatory Compliance
Medivigilax Research delivers the pharmacovigilance and drug safety support to pharma, biotech, and medical device firms worldwide. As Medivigilax Research, we work as a PV outsourcing partner by delivering end-to-end drug safety solutions across the product lifecycle. Our compliance-first approach ensures alignment with global health regulations, reduces risk, and keeps organization inspection-ready, so Businesses can focus on growth with confidence.
End-to-End Lifecycle Support
Pharmacovigilance System Setup & Maintenance
Establishing and maintaining robust pharmacovigilance systems tailored to global health regulatory requirements.
QPPV/PvOIC/Deputy QPPV
Qualified Person for Pharmacovigilance (QPPV/PvOIC) is responsible for ensuring continuous oversight, regulatory compliance, and effective management of global drug safety systems.
Global Literature Monitoring
Literature monitoring involve the systematic monitoring, identification, and assessment of safety information related to medicinal products from medical and scientific literature.
Adverse Event Reporting & Submission
Collection and processes of an adverse events for pharmaceuticals, herbal products, bio-similars, and vaccines products. This involves the identification, assessment, and documentation of adverse events and other safety-related information.