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Full or partial Clinical Trial Development Services (full service limited to phase I and II trials). Services include: Regulatory, Medical Writing, Drug Packaging/Labelling, Clinical Monitoring, Project Management, Data Management, Call Center for patient recruitment, Biostatistics, feasibility studies, notice readability studies, Pre- & Post CE-marking clinical investigations.
Full or partial Clinical Trial Development Services (full service limited to phase I and II trials). Services include: Regulatory, Medical Writing, Drug Packaging/Labeling, Clinical Monitoring, Project Management, Data Management, Call Center for patient recruitment, Biostatistics, feasibility studies, notice readability studies.
The translation, writing and review of clinical documentation. Clinical documentation includes patient information & consent form, patient diary, protocol, CRF, etc.
CRA placement in/outsourcing or permanent according to need.
We offer a full spectrum of services geared to the creation of task-ready, effective CRAs, and the on-going development of skills and knowledge of existing CRAs – in order to more effectively meet our major pharma/medical device clients’ human resource needs and consistently add value to their human resource investment.
For group CRA and GCP training CROPHA enjoys privileged access to state-of-the-art training facilities at the APTASKIL LEARNING CENTRE in Seneffe, Belgium or in-house.
Full course details, dates and enrolment forms can be found on the Aptaskil website.
Participants are limited to 12 per training session. Training material is in English, but training is given in French (or in other languages on request). Most other training services can be effectively achieved at our customers’ premises.
