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 | Sep 16, 2010 | Development of a Clinical Study Report - 3-Part Online Training Series | Online |
 | Sep 17, 2010 | Quality of Active Pharmaceutical Ingredients | Mumbai |
 | 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 19, 2010 | The Art of Writing a Clinical Overview - 3-part Online Training Series | Online |
| Oct 23, 2010 | 5th Annual Conference on Drug Discovery and Clinical Development Meeting the Challenges of Next Generation R&D: Enhancing Efficiency, Effectiveness and Innovation | Bangalore |
| Oct 28, 2010 | Contributing to High-performance Biopharm Teams - 6 Part Online Training Series | Online |
| 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 |
 | Sep 17, 2010 | HALF DAY TUTORIAL WORKSHOP I - WORKSHOP ON CEPS (CERTIFICATION PROCEDURES IN EUROPE) | Mumbai |
| Sep 17, 2010 | HALF DAY TUTORIAL WORKSHOP I - WORKSHOP ON WHO PREQUALIFICATION PROGRAMME FOR PRIORITY MEDICINES | Mumbai |
| Oct 23, 2010 | Tutorial 1 | Bangalore |
| Oct 23, 2010 | Tutorial 2 | Bangalore |
| Oct 23, 2010 | Tutorial 3 | Bangalore |
| Oct 23, 2010 | Tutorial 4 | Bangalore |
| Oct 23, 2010 | Tutorial 5 | Bangalore |
| Oct 23, 2010 | Tutorial 6 | Bangalore |
| 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 | |
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