Human Factors and Usability Engineering in the Development of Drug Delivery Products focuses on incorporating human factors and usability engineering into the development of drug delivery products to ensure compliance with regulations such as MDR, IEC 62366, and FDA guidelines.
Topics
- Understanding the requirements of IEC 62366 and FDA human factors guidance
- Providing regulators with specific usability data for your device
- Validating combination products
- Considering human factors and risk in product development
- Human factors and the design process
- Generic combination products – ANDAs and human factors
- Human factors data required for biosimilars
Who should Attend
- Professionals in engineering and device development
- Regulatory affairs experts
- Quality assurance and quality systems professionals
- Risk management specialists
- Packaging and marketing professionals
- Experts in usability and human factors engineering
