Find us on...
Upcoming webinar on borderlines highlighting medical and biocidal classifications.
Product classification is essential to understand the regulatory requirements applicable to each individual product. It allows companies to understand their legal compliance requirements, ensures products are safe, and protects consumers from being misled into believing products may have functions which they do not.
To classify products, each regulation will contain definitions of the products included within their scope. Classifying products under these definitions usually relies on a series of fundamental factors which need to be assessed on a case-by-case basis.
CTPA is hosting a webinar on 1 August 2024, joined by the Medicines and Healthcare products Regulatory Agency (MHRA) and the Health and Safety Executive (HSE), to look at specific borderline examples with medical and biocidal products.
This webinar is free to join for CTPA members and non-members. Find more information and register here.
