Category: News

Top Regulatory Services Company – 2024

Navigating the intricate realm of life sciences demands a paradigm shift in regulatory outputs and documentation, a need recognized by Glemser Technologies. The recent feature in Life Sciences Review Magazine applauds our commitment to modernizing pharmaceutical regulatory processes. In a landscape where speed is paramount, Glemser employs ComplianceAuthor AI, a cutting-edge, GxP-compliant solution. This cloud-based […]

Written by on January 24, 2024

Proventa International Regulatory Affairs Strategy Meeting

KEY TAKEAWAYS Generating regulatory content is complex and organizations are struggling to keep pace with the volume of data Automation tools are rapidly popping up in the market, making it difficult for the industry to sift through and evaluate the quality of these tools – not all AI is made equally Organizations are seeking tailored […]

Written by on May 30, 2023

DIA Regulatory Submissions, Information, & Document Management Forum

What You Need to Know Navitas Life Sciences, a leading provider of technology enabled services to life science companies, partnered with Glemser Technologies to bring innovations and technology advancements in global labeling to the life science industry. Representatives from each company attended the DIA Regulatory Submissions, Information, and Document Management Forum. The event brought together […]

Written by on March 3, 2023

Navitas Life Sciences & Glemser Technologies Announce Partnership

Navitas Life Sciences, a leading provider of technology-enabled services to life science companies, and Glemser Technologies announced their partnership today, February 6, 2023, bringing innovations and technology advancements in global labeling to the life science industry. The direct integration between Navitas Life Sciences’ labelREADY solution, supporting end-to-end labeling management, and Glemser’s software product, ComplianceAuthor™ Solutions, […]

Written by on February 6, 2023

Summary of product characteristics (SmPC) – Detecting and Managing Updates in SmPC

TL;DR SmPC is a Summary of Product Characteristics, it is the main structure for explaining pharmaceutical products’ characteristics in the EU. SmPC is a legal document used by healthcare professionals that provides information on the drug including the set dosage and other key information. Due to the volume of label changes per year (tens of […]

Written by on May 3, 2022

Quark & Glemser Prescribe Structured Authoring as Part of Content Automation

Quark Software today announced its strategic alliance with Glemser, an IT solutions and services provider to the global life sciences and pharmaceutical industry. The software providers are helping enterprises in this particular vertical market achieve regulatory compliance, while also improving quality, gaining operational efficiencies, and reducing costs. Global labeling improvements and readiness for Identification of […]

Written by on December 15, 2021