Validation, Commissioning & Design White Papers & Case Studies
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IT Changes Implemented To Overcome Future Manufacturing Challenges
2/27/2023
Learn how Pfizer and Ferring improved their reporting and batch information management with Rockwell’s technology.
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Computer System Validation (CSV) To Computer Software Assurance (CSA)
1/24/2023
Learn about the shift from Computer System Validation (CSV) to Computer Software Assurance (CSA) and the intent of this transition in approach to validation in the life science industry.
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Validated HPLC-UV Method For Quantification Of Paxalisib
1/18/2023
Examine research into the development and validation of a HPLC method for the quantitation of paxalisib in mouse plasma and its potential use for routine therapeutic drug monitoring.
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Prioritizing Innovation To Get Ahead Of The Market
1/10/2023
In the pharmaceutical industry, innovation and administration are in a constant tug of war. How can you better manage routine administration tasks that steal 40% of your team's valuable time?
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Time Is Money: The Hidden Cost Of Inefficient Laboratory Practices
1/10/2023
Explore the main inventory management challenges faced by fast-paced biotech and pharmaceutical laboratories and how they directly impact research outcomes, costs, and regulatory compliance.
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Validated LC–MS/MS Method For The Determination Of Copanlisib
11/14/2022
Review study findings on a validated LC–MS/MS method for quantifying copanlisib from a mouse dried blood spot and its potential for enabling desirable sensitivity, accuracy, and precision.
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How Secure Is the Cloud for Pharma Manufacturers?
10/17/2022
Explore if the cloud is secure for pharma manufacturing and if the technology can really deliver on its promise to streamline operations.
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Eliminating Data Integrity Errors Through Digitization
10/17/2022
Explore the urgent need for businesses to adopt strong data integrity practices and identifies measures for how to achieve and sustain compliance.
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Product D-Value Study - Part 2, Heat-Sensitive & Atypical Aqueous Liquids
10/5/2022
How can your organization use this critical tool when developing your sterilization process for heat-sensitive products and low F0 cycles?
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Why Perform A Product D-Value Study?
10/5/2022
Follow our discussion on non-heat sensitive aqueous liquid product sterilization and the use of the Overkill method and Bioburden/BI method.