Available Courses

Results (28)




Course Title Course Date Location
CMC Regulatory Compliance for Biopharmaceuticals, Biosimilars and Other Biologics May 08, 2017 - May 10, 2017 Berlin, Germany
Preparation of FDA Submissions and Communicating with the FDA May 11, 2017 - May 12, 2017 Berlin, Germany
Preparing the CMC Section for MAAs-IMPDs May 15, 2017 - May 16, 2017 Berlin, Germany
Design Control for Medical Device Professionals™ May 30, 2017 - May 31, 2017 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Jun 01, 2017 - Jun 02, 2017 Berlin, Germany
Auditing for Medical Devices: ISO 19011:2011 Framework Jun 05, 2017 - Jun 07, 2017 Berlin, Germany
Auditing for Medical Devices: EN ISO 13485:2016 Changes Jun 07, 2017 - Jun 09, 2017 Berlin, Germany
Introduction to Effective Medical Writing Sep 25, 2017 - Sep 26, 2017 Berlin, Germany
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Sep 27, 2017 - Sep 29, 2017 Berlin, Germany
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 12, 2017 - Oct 13, 2017 Berlin, Germany
European Union Regulatory Issues – New Product Development™ Oct 16, 2017 - Oct 17, 2017 Berlin, Germany
Integration of Risk Management Principles and Activities into the Quality System Oct 16, 2017 - Oct 17, 2017 Berlin, Germany
Filing Variations in the European Union™ Oct 18, 2017 - Oct 19, 2017 Berlin, Germany
Process Validation for Medical Devices Oct 18, 2017 - Oct 20, 2017 Berlin, Germany
Water Purification Systems for Regulated Industries Oct 23, 2017 - Oct 24, 2017 Berlin, Germany
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development Oct 24, 2017 - Oct 26, 2017 Berlin, Germany
Heating, Ventilation, & Air Conditioning (HVAC) in a Regulated Environment Oct 25, 2017 - Oct 27, 2017 Berlin, Germany
Auditing and Qualifying Suppliers and Vendors™ Oct 30, 2017 - Oct 31, 2017 Berlin, Germany
Formulation Design and Troubleshooting of Dry Dosage Forms (Tablets and Capsules) Oct 30, 2017 - Oct 31, 2017 Berlin, Germany
Granulation, Tableting and Capsule Technology Nov 01, 2017 - Nov 02, 2017 Berlin, Germany
FDA Inspections: What Regulators Expect and How to Prepare Nov 06, 2017 - Nov 07, 2017 Berlin, Germany
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Nov 08, 2017 - Nov 10, 2017 Berlin, Germany
Good Laboratory Practices (GLP) for Pre-Clinical Testing Nov 13, 2017 - Nov 15, 2017 Berlin, Germany
QbD: Product and Process Optimization using Design of Experiments (DoE) Nov 22, 2017 - Nov 24, 2017 Berlin, Germany
Best Practices for an Effective Cleaning Validation Program Nov 29, 2017 - Nov 30, 2017 Berlin, Germany
European Regulatory Procedures - Comprehensive Overview of EMA and National Requirements™ Dec 04, 2017 - Dec 05, 2017 Berlin, Germany
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ Dec 11, 2017 - Dec 12, 2017 Berlin, Germany
Writing Effective SOP and Other Process Documents Dec 13, 2017 - Dec 14, 2017 Berlin, Germany