PHARMACOVIGILANCE CONSULTINGSERVICES
Overview
Why
Pharmacovigilance Matters:
Ensures drug safety for patients
Maintains regulatory compliance across India, USA, and Europe
Reduces risks of penalties and delays in drug approvals Supports pharmaceutical, biotech, and CRO operations
GLOBALREGULATORYLANDSCAPE
Key Authorities:
India: CDSCO
USA: FDA
Europe: EMA
Our Goal: Seamless compliance with local and global regulations
OUR PHARMACOVIGILANC
GLOBALREACH
India: Clinical trial support, regulatory reporting, PV audits
USA: FDA compliance, IND safety reporting, PV audits
Europe: EMA-compliant PV services, signal detection, risk management
Key Advantage: Local expertise + global standards
WHYCHOOSEATVIGILX?
Experienced PV professionals with international exposure
End-to-end pharmacovigilance
solutions Regulatory compliance across India, USA, Europe
Customizable services for pharma, biotech, and CROs
Benefit: Reduced regulatory risk and enhanced patient safety
FAQS
1. What are PV consulting services?
A.Expert services for drug safety and compliance
2. Why is PV consulting important globally?
A.Ensures adherence to FDA, EMA, CDSCO regulations
3. How does Atvigilx support regulatory compliance?
A.Through audits, SOPs, training, and ICSR reporting
4. Can Atvigilx handle PV for clinical trials?
A.Yes, pre- and post-marketing trials, including adverse event reporting
FINALTAKEAWAY
Atvigilx provides expert PV consulting services for India, USA, Europe
Strengthens PV systems, reduces risks, ensures global compliance
Ready to streamline your pharmacovigilance processes? Contact Atvigilx today Website: www.atvigilx.com
Email: info@atvigilx.com