Clinical trial authorization from ethics committees and authorities
Review of key areas of the directives and implementing texts
Safety reporting & GCP inspections
Update on current guidance documents, Trial Master File and archiving
Upcoming regulations and developments
Who should Attend
Contract Research Organisations (CROs)
Pharmaceutical companies
Site personnel and ethics committee members
Investigators
Regulatory affairs and pharmacovigilance departments within the pharmaceutical industry
People from clinical research
Past Events
Understanding the European Legislation & Implementing the Guidelines 2014 - 28 May 2014, European Centre for Clinical Research Training (ECCRT), Brussels, Belgium (45181)
Important
Please, check "Understanding the European Legislation & Implementing the Guidelines" official website for possible changes, before making any traveling arrangements
