ProPharma Pharmacovigilance

  1. Qualified Person For Pharmacovigilance (QPPV) 8/8/2024

    Gain expert guidance and connect with a global network of qualified QPPVs and LPPVs, who will ensure compliance with pharmacovigilance regulations and tailor their approach to your product launch strategy.

  2. Signal Management Services 8/2/2024

    ProPharma has deep expertise across all signal detection and management activities, including validation, prioritization, and assessment using data from a wide range of sources that are relevant for signal detection for the individual product(s). We are also fully trained and experienced in the EudraVigilance Data Analysis System (EVDAS) functionality and can support MAHs to comply with their obligations for signal detection and management. We leverage our robust knowledge to select the most efficient and effective method(s) for each product that is compliant with legislative requirements.

  3. Enhancing Global Medical Information Support 6/4/2024

    In the rapidly evolving and interconnected healthcare landscape, the need for a cohesive and responsive medical information system is imperative.

  4. Achieving Success With Regulatory Intelligence In PV 6/4/2024

    Crucial for compliance with evolving standards, take a moment to review ProPharma's range of services to help companies stay up-to-date with regulatory requirements as it relates to intelligence in pharmacovigilance.

  5. The Essential Guide To Local Person For PV 6/4/2024

    For all marketing authorization holders, ensuring a functional pharmacovigilance system is crucial. Make sure you have the right Local Persons for Pharmacovigilance (LPPVs) in the right place at the right time.

  6. The QPPV: A Guide For The Qualified Person Responsible For PV 6/4/2024

    Ensure compliance with EU and UK pharmacovigilance requirements by setting up a robust PV system with a Qualified Person Responsible for Pharmacovigilance (QPPV).

  7. Building Comprehensive PV Programs Around A Single Safety Database 6/3/2024

    Pharmacovigilance is complex enough without your provider adding to the burden. Ensure a smooth process by being forward-thinking, investing wisely, and questioning everything.

  8. Product Quality Complaint Management 6/3/2024

    With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

  9. Accelerate European Market Access With MAA Submission 6/3/2024

    Discover how ensuring preparedness for Marketing Authorization Application (MAA) approval can streamline your application process and subsequent follow-up.