6th Annual Pre-Filled Syringes & Injectables Summit

6th Annual Pre-Filled Syringes & Injectables Summit is organized by Vonlanthen Group of Companies and will be held from Nov 26 - 27, 2020 at Vienna, Wien, Austria. Who Should Attend:Chief Executives, Directors, Vice Presidents, Department Heads, Leaders, Senior Managers, Principal Scientists, Chemists and Engineers specialising in:• Bioprocess Research & Development• Business Development• CMC• Combination Products• Container Development• Controls & Robotics• Device Development & Manufacturing• Device Engineering & Design• Drug Delivery & Devices• Drug Development• Drug Packaging• External Supply• Extractables & Leachables• Fill/Finish• Formulation Sciences• Human Factors• Injectables• Materials Development• Medical & Connected Devices• Parenterals• PFS• QA/QC• Regulatory Affairs• Research & Development• Risk Management• Stability• Standardisation Science• Smart Devices• Sterile Products• Vaccines• Validation Description:During the 2-days networking experience, we will discuss the demand for efficient and convenient-to-use drug delivery devices that are used to improve patients’ experience and the key factors for the market growth advancing the technology. The demand for efficient and convenient-to-use drug delivery devices and improving a patient's experience are key factors for the market growth advancing the technology. This event has been designed for industry leaders to disclose new horizons and developments in pre-filled syringes (PFS) and injectable devices. Attending this event will provide a broad overview of current and upcoming EU MDR regulatory require­ments, innovative technologies, the impact of digitalisation, market trends and device needs. We will discuss the benefits of PFS and injection devices as the main factor for dosage ac­curacy, convenience and safe treatment for patients. They are excited to be hosting the 6th edition of our Pre-Filled Syringes & Injectables Summit and look forward to meeting you in Vienna in November! Key Practical Learning Points:• Overview of the upcoming EU MDR regulation and the role of notified bodies• Devices for self-injection: engineering challenges, trends and new developments• Strategic design: enhancing differentiation through a style guide• Integrating quality requirements• Analytical studies and chemical safety assessment• Manufacturing and processing technologies• The route to digital: the rise of digital therapeutics, and the new associated product landscape• Post-marketing safety reporting View All10 Speaking Bastiaan DeLeeuw Biotechnology Ian Thompson Biotechnology Shruthi Vidyasagar Biomechanics Mike Tate Psychology