Pacific BioLabs is grateful for the opportunity to have collaborated with SteriTek and MediZap on the recent Zap+Learn webinars. SteriTek is a leading provider of E-beam and X-ray sterilization services, […]

The United States Pharmacopeia (USP) has published a new general chapter, the USP <60> which will become official on December 1, 2019. The chapter specifies tests to determine the presence […]

Fourier-transformed infrared spectroscopy, also known as FTIR, is a method of analyzing both organic and inorganic materials, and can provide a breakdown of their molecular makeup. Using FTIR, one can analyze […]

As you may be aware from our previous blog post, the European Union published the new Medical Device Regulation (MDR) on May 5th, 2017 and it is expected to be […]

The European Union published the new Medical Device Regulation (MDR) on May 5th, 2017 and it is expected to be enforced starting May 25th, 2020.  This new regulation repeals the […]

Pacific BioLabs and Nutek used to work closely together to perform the microbiology and sterilization needed for medical device sterilization validation programs.  Nutek was bought out by BART and the […]

Demand in the market for quality textiles that meet consumers’ demands for comfort and freshness has been increasing.  Antibacterial performance depends on its ability to inhibit the growth of bacteria.  […]

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 […]

If you have a product that will be on the market, it is advised that you have proof that it is free from microbiological contaminants.  Antimicrobial preservatives are substances added […]

Why is an effective environmental monitoring program so important? In the end, whether you are manufacturing a medical device or a drug API, the safety of end users is at stake. […]