| 15.03.2010 - 16.03.2010 | Validation of Computer Systems Berlin, Germany | |
| 16.03.2010 - 19.03.2010 | World PharmaTRIALS ASIA 2010 Terrapinn | |
| 18.03.2010 | SwAPP Exchange: Clinical Trials Berne Veranstalter: SwaPP | |
| 08.04.2010 - 09.04.2010 | Project Management for Phase 1 & 2 Clinical Trials Dublin, Ireland | |
| 12.04.2010 - 13.04.2010 | Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process Dublin, Ireland | |
| 12.04.2010 - 13.04.2010 | Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Berlin, Germany | |
| 12.04.2010 - 14.04.2010 | Technical Writing for Pharmaceutical, Medical Device and Biotech Industries Berlin, Germany | |
| 13.04.2010 - 15.04.2010 | MoT: Clinical Trial Management and Regulatory Affairs Lausanne Veranstalter: EPFL | |
| 14.04.2010 - 16.04.2010 | CMC Regulatory Compliance for Biopharmaceuticals and Biologics Berlin, Germany | |
| 15.04.2010 - 16.04.2010 | Writing Effective Standard Operating Procedures and Other Process Documents Berlin, Germany | |
| 19.04.2010 - 21.04.2010 | cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices Dublin, Ireland | |
| 19.04.2010 - 21.04.2010 | QA/QC Strategy for Biopharmaceuticals and Biologics Berlin, Germany | |
| 19.04.2010 - 20.04.2010 | Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries Berlin, Germany | |
| 20.04.2010 - 21.04.2010 | Regulatory Affairs in Central and Eastern Europe Budapest Veranstalter: Informa Life Sciences | |
| 22.04.2010 - 23.04.2010 | Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Dublin, Ireland | |
| 22.04.2010 - 23.04.2010 | Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications Berlin, Germany | |
| 22.04.2010 - 23.04.2010 | Introduction to Effective Medical Writing Berlin, Germany | |
| 26.04.2010 - 27.04.2010 | The EU Clinical Trial Directive Berlin, Germany | |
| 26.04.2010 - 27.04.2010 | FDA Inspections of Clinical Data Systems Dublin, Ireland | |
| 28.04.2010 - 29.04.2010 | European Filing & Registration Procedures Berlin, Germany | |
| 06.05.2010 - 07.05.2010 | The EU Pharmaceutical Law Forum Brussels Veranstalter: Informa Life Sciences | |
| 17.05.2010 - 18.05.2010 | Practical Methods for Project Management Berlin, Germany | |
| 19.05.2010 - 21.05.2010 | Root Cause Analysis for CAPA Berlin, Germany | |
| 24.05.2010 - 25.05.2010 | Clinical Trial Design for Medical Devices Berlin, Germany | |
| 24.05.2010 - 25.05.2010 | Overview of FDA Regulatory Compliance for Medical Devices Berlin, Germany | |
| 26.05.2010 - 28.05.2010 | Process Validation for Medical Devices Berlin, Germany | |
| 26.09.2010 - 30.09.2010 | DC2010: Forum on Vaccine Science Lugano |