📢 Official Announcement | Pharmacovigilance & Regulatory Compliance

CMPV Consultancy LLP is now registered on ADRMS (Adverse Drug Reaction Monitoring System) —
an indigenous pharmacovigilance software developed by the Government of India.

ADRMS is a robust and regulatory-compliant platform, offering a reliable and efficient alternative to global PV databases such as Argus and ARIS G, specifically designed to meet Indian regulatory requirements.

✅ What this means for our clients:

• 📄 ICSR submission in E2B XML format
• 🏛️ Direct reporting to the Government of India
• ⚙️ Compliance with national pharmacovigilance and materiovigilance guidelines
• 🔐 Secure, standardized, and transparent safety data handling
• 🇮🇳 Support for India’s indigenous digital regulatory ecosystem

🔍 Our Services via ADRMS include:

• Individual Case Safety Report (ICSR) processing
• E2B XML case creation and submission
• Quality review, medical coding & case assessment
• Regulatory-compliant safety reporting for drugs & medical devices

By leveraging ADRMS, CMPV Consultancy LLP ensures timely, accurate, and compliant safety reporting, supporting public health surveillance and regulatory decision-making in India.

📣 Partner with CMPV Consultancy LLP for reliable pharmacovigilance solutions aligned with Government of India initiatives.

—
CMPV Consultancy LLP
Pharmacovigilance & Regulatory Experts