Safety Assessment and Biocompatibility Evaluation: Medical Devices and Combination Products

11/06/2014 - 13/06/2014

Safety Assessment and Biocompatibility Evaluation for Registration of Medical Devices and Combination Products

 

Course Topics Include:


• Principles of Testing Materials
• Products for Biocompatibility and Safety
• Regulatory Requirements for Development
• Marketing Approval of Medical Devices
• The Impact of FDA’s GLP Regulations
• ISO Requirements
• Regulatory Path to the Clinic and Market
• Combination Products
 

 

To be presented at:

Parc Cientific de Barcelona

Baldiri Reixac 10

08028 Barcelona

Spain

 

For complete course information please see course brochure or call:

Tel: +34 934487156

e-mail: info@sitec-pharmabio.com