Requirements management in medical device development is a mandatory process, and even for non-medical developments, it is the best approach to ensure you're designing the right product.

By properly defining, writing and verifying against requirements, you can demonstrate your product is functional, safe and has avoided unnecessary costs. 

In this Tekki Brekki, Richard Gold from Kinneir Dufort will provide an overview of best practice in requirements management from personal experience in 10 years of design consultancy.

Richard Gold has 10 years' experience working within design consultancy, spanning a diverse range of sectors including medical, life-sciences, consumer and industrial. This has provided experience developing a wide variety of products from low-power wearables to large electromechanical systems.

Kinneir Dufort is an expert partner, helping companies research, innovate and develop new products and brand experiences.

To register for this free event please email Julie on the link below.

Teas/Coffee and Danish provided.

If you require a parking space please also provide your car registration.