Pacific BioLabs have been performing reusable device cleaning validations for over a decade.  Traditionally, PBL has performed cleaning validations by testing three devices over three different cleaning cycles giving a […]

In March of 2015, the FDA published a new guidance document titled, Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling.  A draft guidance on the same subject […]

Increasingly, device makers are discovering what pharmaceutical companies have known for many years – that using CROs to support regulatory testing can speed up development efforts and, ultimately, save money. The […]

Have no fear! You can access it here in recorded format or as a slide presentation. To provide more information on reusable device validations, Pacific BioLabs conducted a webinar on reusable […]

Background Scientific advances in both diagnostic and therapeutic medicine have led to the development of new and sophisticated reusable medical devices and instruments for use by health care practitioners and for […]