Injectable Drug Delivery 2020

SMi Group is pleased to announce the third annual Injectable Drug Delivery conference, which will be held in London on the 13th and 14th May 2020.

Part of Europe’s leading Injectable conference series, Injectable Drug Delivery will assess innovations in drug product formulation and biologics, innovations in device design, quality management and connectivity for enhanced subcutaneous delivery.

With rapid developments in the parenteral space, the injectable drug delivery market is set to reach USD 902.3 billion by 2027, with an increased focus on patient centricity during DDC development and innovations in device development, including new therapeutic applications such as the delivery of siRNA. This year’s event will focus on advances in drug product formulation and innovations of device design and development to aid delivery.

Furthermore, the conference will assess the evolving regulatory environment of injectable drug delivery with industry and regulatory representatives presenting updates on current guidelines.

The two-day agenda also offers peer-to-peer networking with Global Product Managers, Device Testing Managers, Senior Device Engineers, Heads of Device Development, Heads of Formulation and Drug Process Development, and many more.

The benefits of attending:

This conference offers a chance to learn about innovative injectable drug delivery systems with industrial insights on the following:

DELVE into the latest work in complex formulation for subcutaneous delivery
BENCHMARK against leading pharma companies working to enhance device design and development
UNDERSTAND the regulatory environment of the injectables space from leading regulatory and industry advisors
ENGAGE in industry case studies on design controls, human factors and parenteral formulation
EXPLORE advances in connectivity and human factors key learnings in two pre-conference workshops

Who should attend:

Executives, Directors, VPs, Heads, Principals, Managers, Scientists, Researchers of:

Autoinjectors
Wearables
Device Engineering
Human Factors
CMC
Injectables
Sterile Manufacturing
Packaging
Regulatory Affairs

Featured Speakers:

Alexander Zuern, Device testing manager, Novartis International AG
Andrew Warrington, Project Leader & Patient Advocate, Novartis
Benjamin Werner, Scientist, Boehringer Ingelheim Pharma GmbH & Co. KG
Bjorg K Hunter, Regulatory Manager, Devices, GSK
Blake Green, Senior Manager Regulatory Affairs, Amgen
Camille Dagallier, Formulation and Drug Process Development Senior Scientist, Sanofi
Christopher Muenzer, Senior Device Technology Manager, Novartis
Joel Richard, Head of Technical & Pharmaceutical Operations, MedinCell
Mark Palmer, Scientific Leader, Biopharm Device Engineering, GSK
Rebecca Moses, Director, Core Human Factors Inc.
Rupal Nguyen, Principal Engineer, Allergan
Stefania Ragone, Pharmaceutical Assessor, Medicines & Healthcare Products Regulatory Agency (MHRA)
Tina Arien, Principal Scientist, Janssen Pharmaceutica
Vikas Jaitely, Director, Global Regulatory Affairs Transitional Medicine and Devices, Merck