Act as Qualified Person (QP) in dealing with Pharmacovigilance (PV) activities, and as a local contact person to interact with Medsafe. This ensures that adverse events (AEs) and/or adverse drug reactions (ADRs) are promptly and accurately reported according to Medsafe guidelines. We keep a robust system in place to collect and review safety information.
Patient safety is paramount in healthcare, and pharmacovigilance ensures it remains a top priority. CARSL Consulting offers comprehensive support by acting as your Qualified Person (QP) for Pharmacovigilance (PV) activities and local contact with Medsafe. Our services include:
- Adverse Event (AE) and Adverse Drug Reaction (ADR) Reporting: Prompt and accurate reporting in compliance with Medsafe guidelines.
- Safety Information Management: Maintain a robust system for collecting, reviewing, and managing safety data.
- Risk Management Plans: Develop proactive strategies to identify and mitigate potential risks.
Safeguard your reputation and products with our reliable pharmacovigilance solutions.
