Organizational Change Leadership: Cloud QMS in Weeks, Not Months

Implementing a Quality Management System (QMS) has historically been a time-consuming experience. Now, with the release of Sparta System’s TrackWise Digital, the speed to adopt a QMS has decreased significantly. With Sparta’s QuickStart solutions and organizational change leadership provided by Glemser, customers can adopt a fully digital QMS solution quickly and efficiently in just weeks. […]

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Validation & Configuration Services for Quality Management Solutions

In partnership with Intelex, Glemser Technologies delivers an unmatched quality management approach to the life sciences market that drives performance and lowers total cost of ownership. Glemser brings 30 years of experience helping organizations improve quality, maintain compliance and take advantage of proven technologies and 25 years of successful enterprise compliance software implementations. We help […]

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Apr 18-20: Visit us at EHSQ Alliance Conference 2018

Glemser is a proud silver sponsor of EHSQ Alliance Conference 2018, hosted by Intelex Technologies, in Austin, Texas, April 18-20. The conference will bring together hundreds of Intelex system users and industry experts to learn more about the latest in Environmental Health Safety and Quality. During conference exhibit hours from April 19-20, attendees can visit […]

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Mar 28 Webinar: ComplianceAuthor™ for Clinical Labeling

Join us on Tuesday, March 28th as we introduce ComplianceAuthor™ for Clinical Labeling. The webinar, titled “Avoid High Risk, Non-Compliant Label Content”, will be presented by Tammy Feichtel and features a recent customer case study: a leading global healthcare company who leveraged ComplianceAuthor™ to yield profound value and benefits. The customer determined its manual processes […]

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Mar 15-16: Visit us at Clinical Trial Supply, Barcelona

Glemser is a proud session sponsor of Arena’s upcoming Clinical Trial Supply (CTS) Europe conference. The conference will focus on incorporating new technologies to meet the demands of more complex, international clinical trial supply chains, and overcoming persistent clinical supply challenges. While in attendance, Glemser will introduce ComplianceAuthor™ for Clinical Labeling—our automated solution for end-to-end […]

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Avoid High Risk, Non-Compliant Clinical Labeling Content

Pharmaceutical companies that conduct global clinical trials are required to produce booklet labels that comply with local regulatory requirements by country. A booklet label is a little booklet that is attached to the drug that is being distributed for a clinical trial. A single booklet label must be produced in multiple languages, representing the countries […]

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Upcoming Webinar: Co-Hosted by Glemser and Dell EMC

Join Glemser and Dell EMC on Thursday, November 10 for a live webinar entitled: “Best Practices and Challenges of Selecting and Implementing Electronic Quality Systems.” Presented by Noreen Muscat, Senior Consultant at Dell EMC, attendees will learn how to: Select the right vendor – Learn key criteria for choosing a vendor who can serve as […]

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Boehringer Ingelheim Implements Glemser Technology’s Solution for Increased Efficiency, Compliance, Longevity of Quality Management System

Boehringer Ingelheim is one of the world’s 20 leading pharmaceutical companies, family-owned and founded in 1885 in Germany. It employs more than 47,700 people on all continents and generated net sales of EUR 13,317 million in 2014. In evaluating its quality management processes, Boehringer Ingelheim sought a new, robust system to improve test specifications and […]

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Regulatory Changes on the Horizon: Global Impact of the IDMP

Pharmaceutical manufacturers and CROs face increasingly complex regulatory mandates on the horizon. As requirements increase, so do opportunities for problems with lack of compliance and inconsistent data. To this end, the European Union (EU) is adopting a standard protocol for Identification of Medicinal Products (IDMP) developed by the International Organization for Standardization (ISO). The Move […]

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By the Book: Documentation Requirements in TrackWise

For pharma, CROs, and other the life sciences; even the most useful quality-management tools—such as TrackWise—aren’t without caution and concern. Large system and process-level configurations require large documentation—and it’s important to keep it all in order. Currently in widespread use, TrackWise is a robust system that’s proven flexible enough for different processes through standard configurations. […]

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