Blog

How to Make a Lab Incubator

By Aimee O'Driscoll, 08 March 2021

We take a look at some of the top “instructables” for creating a lab incubator, examining some of the pros and cons of each.

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Rotary Evaporator Accessory Options

By Aimee O'Driscoll, 02 March 2021

A rotovap setup can be quite complex. In this post, we’ll cover some of the most useful rotovap accessories to help you achieve the optimal setup for your application.

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How to Choose a Homogenizer Probe

By Aimee O'Driscoll, 13 February 2021

Selecting the right probe is a crucial step in any rotor-stator homogenization application. We explain the options available and how to choose the right generator for your needs.

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Rotor Stators Versus High Pressure Homogenizers

By Aimee O'Driscoll, 20 December 2020

We compare the pros and cons of rotor-stator homogenization and high pressure homogenization. In addition, we provide a summary of their features and functionality and reveal the types of applications they are most suitable for.

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UL Listing and Other Nationally Recognized Testing Laboratory Markings

Carlton Hoyt By Carlton Hoyt, 26 May 2020

When browsing new equipment, you may often come across the term “UL Listed,” which tends to carry a certain weight in the industry. Or perhaps you have a requirement that your equipment is UL listed. But what exactly does it mean?

Underwriters Laboratories (UL) is a not-for-profit organization that evaluates, tests, and certifies products in the US and Canada. It also has a global reach through partnerships with standards organizations in other regions.

  • US: UL is accredited by the American National Standards Institute (ANSI) in the US, as an audited designator. It is recognized under OSHA’s Nation...

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What are IQ, OQ, and PQ and Why Are They Important?

Carlton Hoyt By Carlton Hoyt, 21 April 2020

Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) are a set of protocols involved in equipment (both hardware and software) validation.  Equipment validation is a critical component of Quality Assurance (QA), as even slight inconsistencies can lead to serious problems.

Using these protocols helps to ensure that QA standards will be met when the equipment is used in product manufacturing. Verification of equipment specifications is required by the FDA and is especially important in highly-regulated industries such as the production of pharmaceuticals and medical devices.

In this article, we’ll go over what is generally involved in the three protocols, including what is bei...

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