Pharmacovigilance
Organisation set-up and changes
For clients who conduct their own pharmacovigilance activities, DADA may function in an advisory role to review the pharmacovigilance system as described in the client's PSMF. If DADA finds topics that may not be inspection-proof, DADA can assist the client with updating the pharmacovigilance system to match Competent Authorities' expectations and legislation.
DADA may also be consulted for advice during the establishment of a pharmacovigilance department at the client, to assist in determining the necessary new communication channels and responsibilities of those departments that will need to interact with the pharmacovigilance department and provide organisational advice if needed.
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
- Local (QP)PV support and AE/MI/PQC processing
- 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