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