Navigating the regulatory landscape, aligning drug-device departments and lifecycle management
Combination Products Forum 2018 will focus on the entire product lifecycle management process from planning, design, implementation, safety & risk assessment right the way through to post market maintenance.
Patients are taking an active interest in their personal health and demanding easy-to-use, integrated delivery and administration systems that are safe to use.
Through a range of workshops, panel discussions, roundtables and case study presentations, key topics will focus on navigating the regulatory landscape, change management & departmental alignment, device development, project management, product usability, human factors, integrating digital platforms and general management across the total product life cycle becoming critical.
Split across three days, the event will focus on one key question: How can you successfully launch and manage a Combination Product!
Sr. Director, Global Value Chain Quality Design
Johnson & Johnson
Associate Director Quality Compliance Combination Products
Global Device Project Leader
Device Development Project Leader
Director Nonclinical Safety Consumer Care
Bayer Healthcare Pharmaceuticals
Associate Director Combination Products and Medical Devices
Regulatory Affairs and Clinical Evaluation Expert
Senior Technical Specialist
Devices Manager I, Device Technology
Head of Corporate Strategy
Senior Manager, Regulatory & Medical Device
Manager, Device Engineering
CMC Product Collaboration Director
Co-Founder and Vice President
Head of Medical Affairs
Associate Director – Human Factors
Attending this event will enable you to:
How to successfully navigate the complex and confusing regulatory landscape at a global level
Internal procedures and change management strategy that will align drug-device departments and partners
An effective Combination Product strategy from initial planning, design, assessment through to post market maintenance
Your combination product!
I am responsible for
I am responsible for
What Others Have to Say
"Extremely valuable, lots of take aways"Senior Manager Software Validation, Biotronik
"It was very interesting, a lot of information to digest, many people with exceptional experience, new trend on the industry. Very good overall!"Medical Software Validation Manager, Teva Pharmaceuticals
"The event was really effective, both as talks and as networking"Director of QA and Regulatory Affairs, Systelab Technologies
"It made us realize our overall status of our products and how we develop them. Interesting to see how other companies work and handled challenges."QA/RA Manager, Synthetic