Parafix FDA registration

Due to the continued growth of our Healthcare market, Parafix are pleased to announce that we are now FDA Registered.

FDA stands for the Food and Drug Administration and is an agency within the U.S. Department of Health and Human Services. Their responsibilities include protecting the public health by assuring that foods are safe, that human and veterinary drugs, vaccines and other biological products and medical products intended for human use are safe and effective.

FDA is recognised worldwide as ‘the’ regulatory body relating to healthcare products. Any business involved in the production or distribution of medical devices intended for use in the United States is required to register annually with the FDA. This essentially means that you cannot market or sell a medical device in the US without it.

FDA registration has provided Parafix with an awareness of the standards to which products intended for distribution in the U.S. are required to meet. Registration standards fit well with the Parafix culture to continually improve and to produce products to the highest quality standards.

Holding FDA registration offers reassurance to our customers that Parafix are committed to good practices in terms of service and quality, whether their products are being sold in or outside of the United States.

Parafix produce a wide range of adhesive solutions for the Healthcare market, using the latest technologies in medical grade materials; find out more about our healthcare markets here or contact us for more information.