Topics
- Value proposition of connected device
- Unpacking Impact of MDR Requirements on the Risk Management Process for integral Drug-Device Combination Products
- Use of simulation and modeling for Combination Products
- Tolerability of larger volume injections from a syringe or autoinjector (not on body)
- Sustainability of a disposable autoinjector and Life Cycle Analysis (LCA) data
- Control Strategy and Essential Performance Requirements
- Particulates in prefilled syringes
- Opportunities and Challenges with the implementation of novel primary packaging of prefillable syringes
- Impurities, Extractables & Leachable: The Perspective of a Toxicologist
- Probability scoring in risk analysis
Who should Attend
VPs, CEOs, Academics and Researchers, Drug developers, CROs, Engineers, Medical Doctors and Scientists involved or interested in:
- Business Development
- Bioprocess Research
- Container Development
- Combination Products
- Device Development
- Controls and Robotics
- Drug Delivery & Devices
- Device Engineering & Design
- Risk Management
- Research and Development
- Vaccines
- Sterile Products
- Extractables & Leachables
- Validation
- Injectables
- Human Factors
- Medical & Connected Devices
- Materials Development
- QA/QC
- Parenterals
- Drug Packaging
- Regulatory Affairs
