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!


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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

Regulatory Affairs

I am responsible for

Device Development

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