Pharmacovigilance
Local (QP)PV support and AE/MI/PQC processing
DADA can provide you with local support staff to receive and process medical inquiries, adverse event reports (see our section on safety reports processing) and product complaints and forward these to the applicable departments within your company. We offer experienced staff to take on the role of local QPPV in selected territories. Through our network of experienced consultants, we can offer this service throughout the EEA.
Services
Other services in Pharmacovigilance
- Audits
- Communication with National Competent Authorities
- EU Qualified Person for Pharmacovigilance (QPPV)
- Expedited reporting
- Global and local literature screening and review
- ICSR/SUSAR processing
- Inspection readiness
- Organisation set-up and changes
- Periodic safety reporting
- Post-Authorisation Safety Studies (PASS)
- PV SOPs and other controlled operating instructions
- PV System Master File (PSMF)
- Risk Management Plans (RMPs)
- Safety Data Exchange Agreements (SDEAs)
- Signal detection and evaluation – benefit/risk assessment in safety review meetings
- Training in pharmacovigilance
- Veterinary PV support
- XEVMPD population and maintenance
Business hours
- Monday – Friday
- 9am – 5pm
- Saturday
- Closed
- Sunday
- Closed