FEATURE ARTICLES
If your company is undergoing a merger, you must juggle operations while ensuring minimal disruptions. You'll need a holistic view of QMS and SOPs to harmonize procedures.
- Single Use In Biopharma: Beyond Savings & Sustainability
- Innovating Bioequivalence: A Novel Approach To Developing Complex Generic Dosage Forms
- FDA Publishes Final Guidance On Reporting Listed Drug Amounts
- 2024 CIO Survey Reveals IT Budgets, AI Priorities For Life Sciences Companies
- Managing Supply Chain Risks Using Relational Risk Analysis
- Designing Highly Agile Bio/Pharma Manufacturing Facilities
- A Quality-Led Approach To Drug Production Facility Design
PHARMA ONLINE WHITE PAPERS
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Systems For Shop Floor Automation And Digitization
We review an automation system that is based on a standard technology platform, with standardized hardware, networking, and software elements and is designed to securely connect to end-user networks.
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Dwell Volume And Extra-Column Volume: What Are They And How Do They Impact Method Transfer?9/22/2022
Understand how system factors like dwell volume and extra-column volume contribute to method performance across labs and how this knowledge can increase the success of method transfer.
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What's Next For Our Evolving Workforce?6/29/2022
Learn about three industry survival methods that, when applied, can ensure generational workforces are blending cohesively: engagement, culture, and communication.
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β-Glucan As A Process-Related Impurity In Biopharmaceuticals5/17/2022
In this white paper, we dig deeper into the sources of β-glucan, its influence on manufacturing and patient safety, and ways to detect and control its amounts in the finished drug product.
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Match Your Development And Manufacturing Path To Your IND Milestones2/17/2023
The drug development journey is long, expensive, resource straining, and risky. Discover how to maximize the value of early phase material and match your development path to your IND milestones.
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Purity Analysis Methods For Synthetic Prime Editing Guide RNAs9/8/2023
Develop a fast, easy workflow for the purity analysis of complex pegRNA molecules along with a robust denaturing technique for pegRNA with high levels of secondary structure.
PHARMA ONLINE APP NOTES & CASE STUDIES
- Overcoming Supply Chain Roadblocks To Ensure Reliable Complex OSD Delivery
- Apheresis Variability Control In Cell Therapy Manufacturing
- The Journey To AAV Production In Suspension – Scaling-Up Your Process
- Successfully Transfer Methods While Using Different Vendor’s Equipment
- High-Throughput Characterization Of RNA
NEWSLETTER ARCHIVE
- 04.25.24 -- Designing Highly Agile Bio/Pharma Manufacturing Facilities
- 04.24.24 -- Pharmaceutical Equipment Sourcing Strategies To Reduce Costs And Risks
- 04.24.24 -- Outsourcing Best Practices To Increase Efficiency And Compliance
- 04.23.24 -- Maximizing Biologics Potential Through Integrated Services For Faster Timelines
- 04.23.24 -- FDA Publishes Final Guidance On Reporting Listed Drug Amounts
PHARMACEUTICAL ONLINE CONTENT COLLECTIONS
The modern microbiology laboratory is starting to look very different from the laboratory of even 10 years ago. The work will be similar, yet technology will have advanced. Automation, in particular, is taking center stage. Check out the latest e-book from Pharmaceutical Online.
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