Maintenance or Life cycle Management is the continuous adaptation of your authorisation documentation to the current state of research and technology. Tasks such as
- Changes in quality (variations)
- Renewal of authorisations
- Extension of authorisation
are part of the daily routine.
RAC would be glad to strengthen your team that is responsible for preparing and submitting the necessary documents.
In addition, we have the capacity to establish procedures for Pharmacovigilance for your company or to take over any necessary activities. We are glad serve as your QPPV (Qualified Person for PharmacoVigilance).