FrontWell news
Explore company news, strategic partnerships and expert perspectives from FrontWell. Discover how our teams are advancing manufacturing digitalization, laboratory operations and data-driven transformation across regulated industries.
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By Alexander Mitchell, Senior Consultant | Low/No-Code MOM Excellence Problem Statement A standardized Tulip application was built and implemented across 3 customer sites to increase process standardization and minimize the impact of system validation. User requirements and…
By Juan Miguel Cubillas , Project Manager | Project Management Excellence Introduction A global top-five animal health pharmaceutical company initiated a strategic program to enhance and optimize its manufacturing operations through the digitalization of electronic Master Batch…
By Maurada Georgina Darida, Junior Consultant and Denis Bele, Managing Consultant, PAS-X Excellence Our Client and their Challenges In a highly regulated industry where accuracy, traceability and reliability are not negotiable, this company is a pioneer in the biotechnology…
By Dr. Paria Pouyan, Managing Consultant and Nikolas Görg, Consultant Tulip Excellence, FrontWell Solutions Introduction A leading global pharmaceutical company initiated a project to upgrade and optimize its manufacturing processes by adopting a compliant electronic Master…
Our Client and their Challenges In the dynamic world of biopharmaceuticals, this company stands out for its dedication to innovation and patient care. With a focus on treatments across neurology, psychiatry, oncology, and hematology, this company has established itself as a…
Customer Background The customer, a leading biotechnology company, planned to scale up production at its manufacturing facility located in the United States. To achieve this goal, digitalization of the facility’s manufacturing processes was required to enable efficiency, quality…
Introduction In January 2024, the US Food and Drug Administration (FDA) published its Quality Management System Regulation (QSMR) final rule that aligns its requirements with ISO 13485:2016 – requiring that a medical device manufacturer’s quality management system meets…
Overview In highly regulated industries such as pharmaceuticals, medical devices, or aerospace one key aspect of manufacturing is how to handle nonconformities (NCs). In any production process there will be error and uncertainty. Processes will fluctuate, inputs will change,…
Imagine a leading biotech company that specializes in developing vaccines, biopharmaceuticals, and revolutionary cell & gene therapies, they wanted to work smarter, not harder. That's where Tulip Interfaces and FrontWell Solutions came in - a tech platform and an implementation…