7 April 2017: Post Authorisation Safety Studies
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- On 22 August 2017
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Speaker:
– Giovanni Fiori, Scientific Director MediNeos Observational Research
The following topics will be covered during the course:
Definition of PASS
Legal framework
Methodological aspects
Data collection
Data management
Audience Target: Training and updating for professionals working in the field of clinical research, in particular Project Managers, Clinical Trial Managers, Lead CRA and Clinical Regulatory, Startup Specialists.
Location: PAREXEL International, via Turati 28 – Milan
Timetable: 14:00 – 18:00
The registration fee due, per person, is:
€ 100,00 (without VAT) for participants belonging to AICRO member companies;
€ 180,00 + VAT (total € 219,60) for non-members of AICRO.
It is possible to subscribe in the short courses by filling in and subscribing to the appropriate
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