Aim
This is a hands on practical workshop to develop the following skill set:Planning and management of clinical studiesProtection of patients and securing dataLogistic hurdles from clinical trial material distribution to central labChallenge of working in a multinational, multicultural medical environmentQuality management of clinical studiesLegal framework and quality standard
Location & Organization
Organizer
ECPM - European Center of Pharmaceutical Medicine, University of Basel
Co-organizers
PFC Pharma Focus or DIA, Drug Information
Faculty / Teachers
Peter Kleist, GSK, BernKurt Pfister, PFC, Pharma Focus AG, Volketswil/ZürichBrigitte Franke-Bray, DIA Europe, BaselHeidi Rohde-Germann, SGPM, Basel (tbc)
Location / venue
Pharmacenter, University of Basel
Timing & Workload
Duration Three days
ECTS points 1
Frequency Teaching including case studies and workshops
Examination yes
Criteria
Is the course taught in English? yes
Is documentation available? (book, syllabus)? yes
Is the course open for external researchers? yes
Remarks
Compulsory module in ECPM master program Drug Development Sciences
More Information
Categories
Therapeutic Areas: None
Enabling Technologies: None
Methodology: Regulatory affairs
Auxiliary skills: Project management
Target Group
All researchers
Country
CH
City
Basel
More information
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