The life sciences industry is heavily regulated, with stringent standards set by agencies like the U.S. Food and Drug Administration (FDA) and the U.K.'s Medicines and Healthcare products Regulatory Agency (MHRA). Compliance with these regulations is not just mandatory but critical for ensuring product safety and efficacy.
In this blog, PEMAC Director of Sales, Donal Bourke delves into how Computerised Maintenance Management System (CMMS) software can be a vital tool for life sciences manufacturers in maintaining compliance with regulatory requirements.
Life sciences manufacturers are bound by regulations such as the FDA’s Current Good Manufacturing Practice (cGMP) and the MHRA's standards, which necessitate meticulous record-keeping and consistent equipment maintenance. For example, the FDA’s 21 CFR Part 11 sets standards for electronic records and signatures, an area where CMMS can play a crucial role.
CMMS software is pivotal in managing maintenance tasks in compliance with regulatory standards. Here’s how:
In a practical application of CMMS in the life sciences industry, Viatris Ireland, a division of a global pharmaceutical company utilised PEMAC ASSETS CMMS to optimise its maintenance and spare parts management. The implementation of this system resulted in streamlined processes, improved maintenance scheduling, and enhanced inventory control. This led to improved compliance with regulatory standards, significantly enhancing operational efficiency.
In another real-world application of CMMS in the life sciences industry, PEMAC ASSETS CMMS software was integrated with warehouse management software (mpx/WMS) and automated storage systems (Kardex and HÄNEL) at a medical device manufacturing facility. This integration streamlined the spare parts management process, significantly enhancing maintenance efficiency and reducing manual effort. The system improved inventory control and accuracy, leading to cost savings and better compliance with regulatory requirements. This case study showcases the potential of CMMS in optimising maintenance management and ensuring regulatory compliance in the life sciences sector.
Choosing the Right CMMS for Life Sciences
In selecting a CMMS, it’s important to focus on:
CMMS software stands out as an indispensable tool in the life sciences industry, offering a streamlined approach to maintenance management and regulatory compliance. Its ability to automate, document, and standardise processes not only assists in adhering to FDA and MHRA standards but also drives greater efficiency and reliability in operations.
Further Information
To learn more, visit the Life Sciences section of our website, email us at marketing@pemac.com or call +353 1 466 3888.