TechUK are partnering with Triteq to give you a clear insight into getting the balance right – understanding the complexity and maximising the value of design and regulatory requirements for medical devices.
Join Triteq Regulatory & Design experts at TechUK on Thursday 21st April from 2pm for a complimentary presentation on designing and developing a medical device. From wearables to hearables, implants to real-time medical monitors.
This year we can see that pharma, biotech and healthcare will take a leading role in driving the consulting market forward with strong requirements for product innovation, growth strategies and regulatory work.
Triteq supports clients through every stage of product development lifecycle, offering consultancy for product development projects and regulatory affairs. As medical device designers accredited to ISO13485, Triteq identify client requirements and use their experience to look ahead and work through the potential challenges and opportunities. Effective product regulatory compliance-driven innovation provides greater focus at early stage product development enabling product cost reductions and in many cases considerable reduction in development costs and delivery timescales. Increasingly, we are seeing that compliance requirements are actually directly driving the way product innovation happens. Triteq support the generation, development and refinement of your product concept to ensure all of the requirements for commercially and technologically viable products are met.
This event will benefit anyone involved in medical, health and wellbeing, product design, development, commercialisation, production, marketing, sales and distribution.