Sterile packaging components

The new European MDR EU 2017/745 lays down rules concerning med devices being placed on the market for human use. As part of a global harmonization effort, many aspects of the new MDR are aligned with requirements noted in the U.S. FDA CFR's, as well as the recent release of ISO 13485:2016, an international standard governing medical device quality management systems.

Apr 29, 2009

• Ready Pack system is appropriate for small-quantity filling of high-value drugs, pharmaceutical R&D and clinical work, and biopharmaceutical early-stage product development

• includes West VeriSure stoppers and
Flip-Off seals and Ready-to-Fill vials

• sterilized components are delivered in packaging appropriate for aseptic filling

West

West

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Discover the latest breakthrough packaging technologies shaping the pharmaceutical sector. This report dives into cutting-edge innovations, from smart containers that enhance patient safety to eco-friendly materials poised to transform the industry’s sustainability practices. All from PACK EXPO. Learn how forward-thinking strategies are driving efficiency and redefining what’s possible in pharma packaging.

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Products

Sterile packaging components

West

Sustainable Healthcare & Medical Device Packaging Suppliers List

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List: Digitalization Companies From PACK EXPO

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