• Articles

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    Adhering to a tried-and-true set of best practices during the PPQ stage can prevent a drug approval from stalling out on the final lap.
    Michael Annino | Shutterstock-AI
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    How pharma can use CAPA as a tool to support continuous process improvement
    Aging populations are straining pharma production — here’s what the industry should do
    ADMs allow manufacturers to take charge of supply channels to boost efficiency and flexibility
    Pharma manufacturers will need to change their approach if they want to prevent supply chain challenges from rolling over into the new year

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    How intelligence-driven solutions can refine pharma’s quality operations
    It’s essential to examine where the industry stands in regulating drugs and the improvement areas from the dispenser to the patient level
    Droplet digital PCR technology can help catch batches with contamination levels outside of regulatory guidelines
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    A cohesive 2D barcode strategy can drive operational improvements across the pharma ecosystem
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    How the pandemic spurred a technology evolution for temperature-sensitive products
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    How cutting-edge technologies can streamline and enhance equipment validation processes
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    Pharma’s risk assessment needs to go beyond APIs
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    How a robust third-party risk management solution can alleviate drug supply chain pressures
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    How pharma can use digital tools to modernize data integrity
    How Mass Spectrometer Works
    Speed and precision make MS the first choice for the real-time monitoring of fermentation and cell culture off-gas