Pharmacovigilance Services

---

- Flexible for long, medium or short term cover, and willing to support in instances where emergency QPPV cover is required

- The PV team mainly compromises of pharmacists with extensive PV experience

- Deputy QPPVs in  training

- Can perform the investigation of ADR with  the reporter/ patient on your behalf, or review  your report

- Long term or short term support

- Project Management oversight

- UK based QPPV's

- EU based QPPV's

- Creation of PVMFs

- Creation and maintenance of PV Standard Operating Procedures (SOPs)

- Creation of bespoke templates to suit your unique molecules

- Generation of PV agreements

- Provide PV training to your team

- Weekly Literature Searches

- Periodic Safety Update Reports (PSURs)

- Risk Management Plans (RMPs)

- Ongoing signal detection and evaluation

- ADR electronic reporting 

- ADR investigation and medical Information

- Performing internal pharmacovigilance audits

- Performing GAP assessments

- 'Mock' inspections

-  Writing of clear, concise and patient-friendly product information including patient information leaflets (PILs) and primary and Secondary packaging

- Expert advice on design, development and layout of your PILs 

-  Full readability testing