ISO certifies Wasdell Ireland facility for medical device manufacturing

Wasdell Ireland facility has been certified ISO 13485 for medical devices

The Wasdell Group has announced its Dundalk, Ireland facility has been certified to comply with the ISO 13485 standard for medical device manufacturing.

The ISO 13485 denotes the company’s quality management system complies to customer and applicable regulatory requirements.

Earlier this year, The Wasdell Group acquired a specialist packaging supplier to the medical device and pharmaceutical sectors, Planned Packaging Films Limited (PPFL). The ISO standard will further strengthen this offering by providing a base for PPFL services in Ireland.

Graham Wright, MD of PPFL said: “We are delighted that we now have a base in Ireland that can support our continued growth in the medical packaging sector within the UK and Ireland, as well as our export markets.”

Vincent Dunne, CEO at Wasdell, added: “Achieving the ISO 13485 certification allows us to meet the growing needs of customers requiring the medical device standard. It also positions us to support the supply of films and components to existing customers following our acquisition of PPFL that enabled our entry into this space.”

Wasdell already services the European pharmaceutical and biotech sectors from Dundalk with both clinical and commercial packing in packaging formats including syringes, blisters, containers and sachets. It offers end-to-end services across pharmaceutical manufacturing, packaging and storage and distribution.

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