Pharmacovigilance
Safety Data Exchange Agreements (SDEAs)
The QPPV should have oversight of the global safety profile of the MAH's medicinal products. Competent authorities want reassurance that safety information is exchanged effectively between different departments (e.g., Regulatory and Pharmacovigilance), between affiliate and headquarter companies and from one end of your organisation (for instance, your distributor in the Middle East) to the other (e.g., your US headquarters), and that the QPPV will be updated with all safety issues and emerging safety concerns in real time.
These are aspects that are frequently scrutinized (and found wanting) at an inspection. To ensure that global safety information is available at a central point within the EEA, DADA can assist in the creation of safety data exchange agreements: documents shared by business partners (associated manufacturers, marketing partners, distribution networks or vendors) that establish clear responsibilities, communication channels and methods for the exchange of safety information.
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
- 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)
- 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