Medical Device Packaging "Validation Service"

One-stop support from transportation testing to integrity evaluation of sterile barrier systems and stability testing!

Due to the change from the Medical Devices Directive (MDD) to the Medical Devices Regulation (MDR), ISO 11607:2019 has made packaging validation a clear requirement. As a result of this change, integrity testing of sterile barrier systems must be conducted after performance testing of the packaging system and after stability testing. Our service provides a one-stop solution for all necessary tests, from transportation packaging testing to integrity testing of sterile barrier systems and stability testing. This allows you to be freed from the cumbersome ancillary tasks and complicated communications related to inter-site transportation, enabling rapid packaging validation. ▼ For more details, please download the PDF document (recommended). ▼ If you need assistance urgently, please contact us through the 'Inquiry' section below.

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basic information

By using our services, you can gain the following benefits: ◇ We provide a one-stop solution from transportation testing to the integrity evaluation of sterile barrier systems, enabling a reduction in product development lead time and allowing for early entry into domestic and international markets. ◇ With the extensive support of packaging experts, you can focus on your core business. JBL conducts over 300 validations of medical device packaging annually and is a skilled group with extensive knowledge and experience. We have many ISTA-certified CPLP technologists and technicians on staff, and through our alliance with ISTA, we gather the latest information to assist with customer testing.