End-to-End Product Life-Cycle Management
The 3rd Annual Combination Products Forum will focus on the entire product life-cycle management process: From planning, design and implementation, right the way through to post-market maintenance and surveillance strategies.
Patients need for combination products is growing exponentially, and users are demanding easy-to-use, safe products with integrated delivery systems. However, with lack of clarity on regulatory requirements, and huge obstacles to effectively managing product life-cycles, it’s not easy to meet this demand! That’s why we created the Combination Products Forum – designed to help you overcome obstacles at every stage of product life-cycle.
Through a range of workshops, panel discussions, round-tables 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: Can you successfully launch and manage a combination product?
Head, Combination Products CoP and Sr. Director, Global Value Chain Quality Design
Johnson & Johnson
Head of Notified Body
Head of Medical Affairs
Product Safety Manager
Associate Director, Global External QA Operations
Device Project Director
Associate Director, Medical Devices and Combination Products
Director, Nonclinical Safety Customer Care
After Attending You Will Be Able 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!
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