
Smart engineering strategies to future proof your system development
Wednesday, February 18 at 16:00 GMT | 17:00 CET | 11:00 EST | 08:00 PST
Join us for an in-depth session exploring the essential framework that guides life sciences and MedTech products from early scientific concept to sustained, high-volume production. We unpack the critical differences between R&D/assay development and production-ready medical projects, showing how an engineering-led approach anticipates the complexities of regulatory demands, scalability challenges, and long-term data capture.
Learn where early, strategic collaboration creates a decisive competitive advantage, and how addressing the non-obvious challenges early can mean the difference between a promising breakthrough and a reliable, profitable commercial product.
Key learning objectives:
- Recognize and adapt to the fundamental differences between scientific discovery (assay development) and product development (regulatory requirements).
- Understand how early engineering collaboration ensures the instrument development (hardware/software) supports and accelerates potential changes in the assay and data analysis.
- Identify the critical, non-obvious manufacturing and supply chain focus areas that must be addressed early to guarantee a smooth, successful product launch.
- Learn how to leverage Plexus's full-cycle expertise to transform a scientific concept into a high-quality, scalable, and commercially viable product.
Certificate of attendance
If you attend the live webinar, you will automatically receive a certificate of attendance, including a learning outcomes summary, for continuing education purposes. If you view the on-demand webinar, you can request a certificate of attendance by emailing editor@selectscience.net.
Speakers



Moderator

Who should attend?
- Assay development
- Quality & regulatory
- Engineering & technical
- Product & strategy management
- R&D
What will this webinar cover?
- How can product strategy improve efficiency and reduce risk in life science and MedTech system development?
- What are the key considerations when designing flexible systems for evolving assays, data analysis, and regulatory requirements?
- How can engineering teams balance innovation with manufacturability, scalability, and long-term production needs?
- What are the biggest regulatory, manufacturing, and supply chain risks to successful product development? How can they be mitigated early?
- How can early engineering collaboration and cross-functional alignment drive better product outcomes?






