Have you experienced any side effect, adverse event, or safety issue after using a medical device?

Your report is important for protecting public health and improving the safe use of medical devices in India.

🩺 What can be reported?

• Side effects or adverse events following use of a medical device
• Device malfunction, failure, or quality issues
• Injury, health deterioration, or unexpected outcome
• Any serious or unusual safety concern related to a medical device

Medical devices include:
Implants, stents, catheters, syringes, surgical instruments, diagnostic kits, monitoring devices, implants, and other medical equipment.

📩 How to report?

Send details of the adverse event to:
CMPV Consultancy LLP
📧 Email: cmpvconsultancy@gmail.com

🏛️ What happens to your report?

• Reports are reviewed and assessed by pharmacovigilance professionals
• Valid cases are processed and submitted to the Government of India
• Reporting is done through the ADRMS (Adverse Drug Reaction Monitoring System) as per national guidelines
• Data supports medical device vigilance, signal detection, and regulatory safety actions

🔒 Confidentiality & Eligibility

• Patient confidentiality is strictly maintained
• Reports accepted from patients, caregivers, healthcare professionals, and the general public

📣 Your report can save lives.
📣 Report adverse events today and contribute to medical device safety in India.

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CMPV Consultancy LLP
Pharmacovigilance & Medical Device Vigilance Experts