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 | Sep 16, 2010 | Development of a Clinical Study Report - 3-Part Online Training Series | Online |
 | Oct 06, 2010 | Training course on Practical GCP Compliance Auditing of Trials & Systems | London |
| Oct 06, 2010 | Comprehensive Training on European Regulatory Affairs including Different Registration Procedures and Variations: Expert Overview | Prague 8 |
| Oct 12, 2010 | Good Clinical Practices for the Clinical Research Professional - 4 Part Online Training Series | Online |
 | Oct 18, 2010 | Joint DIA-ACT-CST Toxicology Study Director Workshop | |
| Oct 19, 2010 | The Art of Writing a Clinical Overview - 3-part Online Training Series | Online |
| Oct 28, 2010 | Contributing to High-performance Biopharm Teams - 6 Part Online Training Series | Online |
| Nov 04, 2010 | Understanding the Statistical Thinking in Clinical Research for Drug Development | Beijing |
| Nov 05, 2010 | Who's Monitoring the Monitor - 3-Part Online training Series | Online |
| Feb 21, 2011 | Training Course on Excellence in Pharmacovigilance: Clinical Trials and Post Marketing | London |
 | Mar 28, 2011 | Roundtable 01: Inspection and Audit Findings (+7.6%) | Geneva |
| Mar 28, 2011 | Tutorial 02: The 'New' Variation Regulation in Practice – Advantages and pitfalls | Geneva |
| Mar 28, 2011 | Tutorial 03: Orphan Drugs in the EU; From Designation to Marketing Authorisation | Geneva |
| Mar 28, 2011 | Tutorial 04: Regulatory Requirements for the Development of Paediatric Medicinal Products | Geneva |
| Mar 28, 2011 | Tutorial 05: After the PIP Decision: Modification of the agreed PIP, validation and compliance check | Geneva |
| Mar 28, 2011 | Tutorial 06: Successful Outsourcing of Non Clinical Development Programmes | Geneva |
| Mar 28, 2011 | Tutorial 08: Data Privacy in Clinical Trials and Pharmacovigilance | |
| Mar 28, 2011 | Tutorial 09: The New ISO ICSR - ICH 2B Standard | Geneva |
| Mar 28, 2011 | Tutorial 12: Harmonisation of Clinical Trial Regulation in former Russian States with EU Clinical Trial Regulation | Geneva |
| Mar 28, 2011 | Tutorial 07: Introduction to Medical Device Legislation | Geneva |
 | Sep 02, 2010 | Computerized Systems Inspections in the Pharmaceutical Industry | Online |
| Sep 02, 2010 | A Tour of FDA | Online |
| Sep 02, 2010 | Good Laboratory Practices (GLPs) | Online |
| Sep 02, 2010 | GxPs | Online |
| Sep 02, 2010 | HIPAA - The Impact on Clinical Research | Online |
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