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See how to streamline CFR Part 820 compliance for medical devices. Merit for Life Science tackles CAPA, complaints & training for smoother FDA inspections. The post Lessons from 483s: Essential Strategies for Medical Device Manufacturers [https:...
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Worried about FDA inspections? Learn from 483 inspection trends & achieve compliance excellence. This blog series "Lessons from 483 Inspections" unlocks the secrets! The post
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FDA inspections find many biopharma firms struggling with CFR 21 Part 211. Learn how Merit tackles these challenges, ensuring proper procedures and documented incident management. The post
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Imagine the scene: a life science manufacturer eagerly anticipates the launch of a groundbreaking therapy. But suddenly, disaster strikes. In the last of our 4-part series on Optimizing Inventory, Paul takes a look at the importance of storage ...
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In the third post of our 4-part series on optimizing inventory for life science, Paul shares information about Batch and Lot Splitting and Genealogy in Merit for Life Science and how it can provide greater operational efficiency and visibility ...
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In autologous cell and gene therapy, ensuring patient safety and product integrity demands a robust ERP system. In this post, Merit Solutions Solution Architect Benjamin Hart covers the essential features an ERP system needs to ensure a reliabl...
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Discover how cloud platforms like Microsoft Azure with Merit Life Science for Dynamics 365 are reshaping collaboration in medical devices and biopharma. Learn how secure data sharing and real-time decision-making streamline approvals, ensure co...
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Pharmaceutical and biotech organizations require strictly controlled processes to be used when materials are measured out or transferred between containers. Learn how Merit helps improve weighing and dispensing and other manufacturing productio...
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Explore how Life Science CDMOs are embracing cloud computing to stand out in a competitive market. Bill Burke shares 4 reasons why CDMOs are increasingly moving to cloud applications. The post