Recent Articles

AABB 2016 - Orlando, FL

Visit us at the 2016 AABB Annual Meeting!

Mesa Labs would like to invite our customers and friends to visit us at the upcoming AABB Annual Meeting in Orlando, Florida, October 22-25. The AABB Meeting brings together over 5,000 domestic and international blood bank professionals to educate, learn and network with one another. If you are interested in learning more about our continuous…

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CTS 2016 - Princeton, NJ

Visit us at the Clinical Trial Supply East Coast Conference!

Mesa Labs would like to invite our customers and friends to visit us at the upcoming 14th Annual Clinical Trial Supply East Coast Conference in Princeton, New Jersey, October 19-20. The CTS Conference brings together all the leading supply chain personnel to look at the pertinent challenges associated with global supply chains. If you are…

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Vaccines for Children & Vaccine Cold Storage

Are you confident that your vaccines haven’t been compromised? The Centers for Disease Control and Prevention (CDC) Vaccine Storage & Handling Toolkit aims to provide guidance on these and other questions. Published in 2014, the Toolkit discusses Vaccine Cold Chain, Transportation, Storage and Handling Plans, Temperature Monitoring Equipment, Best Practices and more. More recently, the CDC released…

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Global Services

Mesa has created a service network specifically suited to provide in-house services to our customers. Whether your needs call for equipment repair, calibration or process validation, Mesa’s Global Services team is uniquely qualified to bring together the expertise of all Mesa’s products to provide our customers with the specialized service, expert protocol development and execution and complete validation services to suit every need.

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FDA Warning Letters

Aside from maintaining proper working order for your instruments and devices, it is crucial to consistently calibrate and validate your systems in order to meet compliance standards. Sustaining proper documentation and reports is critical when it comes time for audit reviews. Failure to comply with regulations could result in consequences for your company or facility, such as a Form 483 issued against any observed conditions that may violate the Food Drug and Cosmetic Act.

For examples of warning letters, please visit the FDA website here.

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