Medical Device Courses

CfPA offers numerous courses in the field of Medical Devices:

• Advanced Validation and Commissioning for Pharmaceutical,
• Biopharmaceutical and Device Manufacturing
• Biocompatibility Evaluation for Registration of Medical Devices and Biomaterials
• Clean Room Technology
• Clinical Studies for Medical Devices
• Current Good Manufacturing Practices (cGMP) for the Pharmaceutical and Medical Device Industries
• Design Control and Product Validation
• Developing and Managing Complaint Procedures for Medical Devices
• GMP/QSR/QSIT for Medical Devices
• Good Tissue Practices (GTP)
• ISO 13458, ISO 9001 and QSR Regulations for Medical Device Companies
• LAL Testing: Drugs, Medical Devices and Biopharmaceuticals
• Medical Device Regulatory Compliance
• Medical Devices: Strategies for Getting to and Staying on the Market
• Microbiological Control and Validation
• Premarket Submissions for Software Controlled Medical Devices
• Principles of Process Validation
• Process Validation for Packaging of Pharmaceuticals and Medical Devices
• Registration of Medical Devices and In Vitro Diagnostics in Europe
• Root Cause Investigation for CAPA
• Sterilization Technologies and Process Validation
• Validating Medical Devices: Computer Software and Hardware

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