Development & Manufacturing White Papers & Case Studies
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Compatible Platforms For Microbial Identification
11/21/2023
Reduce the time-to-results for microbial identification by taking advantage of the shorter run cycle and off-instrument data analysis provided by this optimized and validated workflow.
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Correlating Stopper Height To Container Closure Integrity
11/21/2023
Learn how to comply with the new EU Annex 1 Section 8.28. Here, we describe a typical raised-stopper investigation and demonstrate how to generate scientifically robust data using headspace analysis.
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Advancing Compliance And Digital Strategy To Align With Pharma 4.0
11/21/2023
AmplifyBio sought to identify areas of its operation where digitalization could yield ROI in a short amount of time. Gain insight into the out-of-the-box solution that aligned with Pharma 4.0.
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Increasing Bioavailability With Amorphous Solid Dosage Formulations
11/10/2023
Discover the challenges associated with pH-dependent solubility for oral tyrosine kinase inhibitor drugs and how leveraging ASD formulation can help create more effective, patient-friendly drug products.
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Reliability Assessments And Benchmarking In Life Sciences
11/7/2023
Gain insight into how a prominent medical device manufacturer observed a significant improvement in its plant-wide OSHA recordable rate and cost of goods savings of over $100,000/year in just one year.
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The Future Of ADC Manufacturing
11/2/2023
Enhance your ADC manufacturing processes by leveraging the performances and inherent benefits of single-use isolators.
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The Role Of The Technical Transfer Executive Sponsor
10/30/2023
Explore the importance of understanding a CDMO’s flexibility and culture, models and scale of equipment, technical capabilities, regulatory support, quality system, and executive sponsorship model.
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Regulatory And Quality Consulting, Operational Readiness Services
10/5/2023
Learn how CAI aided a manufacturing company in merging food regulations with biopharmaceutical technology, allowing for the quick conversion of a small R&D facility into a GMP-compliant facility.
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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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Monitoring And Determining The Cause Of Antibody Discoloration Using cIEF And EAD
9/21/2023
View a study which provides additional insight into the factors that govern the discoloration of protein therapeutics and the role of AGEs in color change.