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Medical Device Packaging & Labeling
Medical Device Packaging & Labeling
Design | Standardize | Implement
Medical Device Packaging & Labeling
Design | Standardize | Implement
Trending
Medical device recalls due to mislabeling and packaging errors are the cause of some major problems in the industry.
Manufacturers are implementing measures to cope with constantly amending regulatory requirements for medical device packaging & labeling in major geographies. As the MedTech industry is consolidating with a greater number of M&As, manufacturers are additionally investing in rebranding, centralizing their enterprise systems, and standardizing their labeling lifecycle. Moreover, medical device manufacturers are exploring sustainable packaging solutions to tackle biomedical waste rampant across the industry.
Opportunities & Challenges
Stringent and constantly evolving regulatory requirements, standardizing the labeling processes across all the newly acquired manufacturing sites or plants, and developing complex yet sustainable packaging solutions.
To cope with the increased regulatory requirements, companies are required to establish cross-functional collaborations, such as R&D, regulatory, quality, etc., to gather essential inputs, thereby ensuring an effective change process.
Increased number of M&As call for standardizing and automating the labeling processes across all manufacturing sites to improve operational efficiency and reduce the discrepancy. Moreover, with the rising eco-consciousness, companies are investing in the development of sustainable packaging solutions to minimize medical waste.
Service Framework
Service Assets
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Standard SOPs & customizable templates as per 21 CFR Part 801, ISO 15223-1:2016, ISO 11607, IEC 60601-1, etc.
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A multi-disciplinary team of packaging & labeling engineers and regulatory experts
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Packaging testing facility to perform underwater leak, compression, gelbo flex, vibration, tensile test, etc.
Differentiators
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End-to-end service portfolio from identifying and adopting the right enterprise LMS, validating the implementation to label creation and verification
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Extensive expertise on tools such as Solidworks, Catia, ArtiosCAD, Prisym, Bartender, Label Vision, etc.
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Strategies for optimizing additional packaging tests through robust rationales
Benefits to the Customer
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Effectively communicating safety, usage, performance, and manufacturing-specific information on the label
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Sustainable packaging for recyclability, biodegradability, and reduced carbon footprint
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Robust and validated packaging ensuring safe and sterilized device out-of-the-box
Discover More
Technical Whitepaper
Impact of EU MDR on Medical Device Labeling
Technical Whitepaper
Unfolding the EU MDR through the Lens of a Remediation Partner
Blog
7 ways how the EU MDR is impacting the global medical devices industry
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