Insights On Quality Assurance
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Optimizing Process Loads For VHP Decontamination
2/20/2024
Explore how CAI helped a company rescue a failing CQV project and create more efficient Vaporized Hydrogen Peroxide Material Air Lock (VHP MAL) Loads to enhance operational efficiency.
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EMA’S eCTD 4.0 Workshop Seeks To Gear Industry For Implementation
4/12/2024
As the EU prepares to implement the new eCTD 4.0 standard for regulatory submissions, the European Medicines Agency (EMA) is taking steps to ensure a smooth transition for industry.
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4 Digital Transformation Gaps In Pharmaceutical Manufacturing
3/30/2023
Take an in-depth look at the pitfalls of manual, paper-based manufacturing processes and why digitization could be the answer for pharma and medtech manufacturing of the future.
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6 Best Practices For Enterprise Quality Management Solutions Implementation
9/8/2022
While all enterprise software implementations are unique we share six best practices that will improve the likelihood of any successful quality management software implementation project.
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Nitrosamine Impurities Deadline: Are Your Products Compliant?
11/6/2023
The FDA nitrosamine contamination guidance set deadlines of Nov. 1, 2023, for risk assessment updates and Aug. 1, 2025, for full NDSRI limit compliance.
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3 Steps To Achieve Total Quality Management In Pharma Manufacturing
2/17/2023
How can your company capitalize on the latest quality management trends by adding Total Quality Management tools to their toolboxes?
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Meeting An Aggressive Go-To-Clinic Timeline
9/27/2023
Finding an outsourcing partner capable of giving your company proper attention and meeting project milestones on schedule is crucial to ensuring patients in need receive treatment in a timely manner.
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Remote Clinical Trial Monitoring: CRA Success In An Era Of Autonomy
4/5/2023
As organizations become more skillful in training and monitoring CRAs, the latter can be empowered with greater flexibility and freedom in scheduling and travel.
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Improving Quality Through Supplier Audits
6/6/2022
Suppliers and manufacturers working together to improve quality throughout the supply chain creates high quality standards to ensure final products are safe and effective.
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Achieving Next-Level Quality With Digital Technology In Manufacturing
9/30/2022
Learn how a modern Manufacturing Execution System (MES) is using digital production records to help manufacturers regulated by the FDA improve their quality and efficiency goals.