The next meeting for GCP-RMA members will be held on 20th and 21st September in Nottingham, UK. Once again, this promises to be an agenda-packed meeting with a wide variety of interesting topics. The agenda has not quite been finalised but currently includes:
- management of pharmacovigilance (PV) records; what is the impact for management of clinical trial master files?
- destruction of original trial documents – what guidance does the DIA TMF Reference Model SIAC have?
- centralised versus decentralised management of sponsor trial records; which approach is best suited to your circumstances?
- third-party document storage vendor selection – a checklist
- third-party document storage vendor selection – what should be in your contract?
- archive tracking systems – a case study
- electronic trial master files (eTMF) – a case study
- member feedback/discussion
- member annual general meeting
This conference is free to attend for GCP-RMA members.
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