Our experienced team can provide a flexible and bespoke pharmacovigilance service designed to meet the complex and changing needs of the global environment.

Whether you are a small generics company or hold multinational licenses with large case volumes, we can offer full PV services including the set-up and maintenance of a full PV system and taking care of all your PV responsibilities (including preparation of all PV documentation, provision of QPPVs, literature searching, signal detection, aggregate data and full case processing using our fully validated database).

UK and EU QPPV and NPC

JensonR+ have QPPV’s based in the UK and Ireland so we can act as both UK and EU QPPV & Deputy as part of a comprehensive PV service or as a standalone service if needed. JensonR+ can also provide NCP service to support your needs.


JensonR+ provide pharmacovigilance auditing services to support you, including Due Diligence support. We can provide a full assessment of systems in use and share advice on areas for improvement.

Bioequivalence Study – Sponsor and Monitoring Function

We offer a scalable service for small Phase 1 studies through to larger post authorisation patient studies.

Medical Device Vigilance

We provide support to manufacturers of devices to ensure a fully compliant post marketing vigilance system.


JensonR+ can provide both general PV or focused training on individual topics, depending on your requirements. Training is bespoke and tailored to your company’s needs, varying from yearly PV refresher to subject specific training from Subject Matter Experts

Global Network

We have a large pharmacovigilance network we can collaborate with and provide vast expertise.

Medical Information

Our experienced team can provide a dedicated, English-language medical information service to supply high-quality, up-to-date information on medicines and medical devices.

Named Patient & Compassionate Use Programmes

We provide services to support monitoring of specific programmes.