Pharmacovigilance Consultancy Services

Pharmacovigilance Consultancy Support

QVigilance has a team of scientific and medical experts with broad experience in all areas of pharmacovigilance. As a result, we can provide guidance and support (including drafting and/or review) in the development/update of Standard Operating Procedures (SOPs)/working practices supporting Pharmacovigilance activities where these are undertaken within your organisation, as:

• All employee PV training
• Safety data exchange agreement authoring and maintenance
• Global safety committee activities
• Signal management and Risk minimisation activities
• Development/Maintenance of company core datasheet maintenance (CCDS) and labelling committee governance
• Safety variations and Urgent safety restrictions
• Handling safety information from product quality complaints and medical enquiries; including safety information from solicited activities (e.g. registries, market research, patient support programs, company’ sponsored social media activities)

In addition, our team can support with:

• On-site or remote development and provision of all employee PV training materials
• Safety data exchange agreements authoring
• Adverse event and pregnancy forms development
• Development of educational materials for risk minimisation and creation of targeted questionnaires for specific patient groups, AEs or other safety concerns
• Benefit-risk communications with competent authorities
• Review/input into clinical trial protocols, investigator brochures and clinical study reports
• On-site or remote regulatory inspection support before, during and after the inspection
• Conducting on-site or remote audits of internal global and affiliate PV departments; as well as audits of contractual partners/providers
• Provision of consultancy support on safety database, including due diligence, set-up, validation and data migration activities