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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

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