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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Critical Considerations For Buffer Preparation
Learn about the steps of buffer development, supply approach and strategy selection, choosing between in-house and outsourcing buffer activities, and other related buffer use topics.
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Intro To USP <1062> - What It Is And Why You Should Use It7/20/2023
Knowing how to use USP <1062> helps manufacturers manage the wide variety of factors that can exacerbate production costs, or result in no product at all.
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2023 Pharmaceutical Manufacturing Trends1/13/2023
Adaptability is the new superpower in pharma manufacturing. By staying on top of these trends, manufacturers will be better positioned for success in the competitive, rapidly evolving pharma industry.
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COGs Process Economics For Autologous Cell Therapy8/11/2023
Analyze the cost distribution over time for autologous CAR T therapy manufacturing using process economics and additional insights. Discover how cell therapy manufacturers can combat these costs.
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Membrane Filter Pore Size Impact On Colony Size, Microbial Recovery1/31/2024
Explore results from a study evaluating the effects of different pore sizes on colony size and microbial recovery using membrane filters.
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Inspection Of Injectable Products For Visible Particulates8/8/2023
Examine the risks posed by particulates, the potential sources and types of particulates, and approaches to detect and measure visible particulates in injectables.
PHARMA ONLINE APP NOTES & CASE STUDIES
- Risk-Based Approach Supports Migration Of Legacy Methods For Eurofins BPT Toronto
- Simplifying Complex Fluorescence Multiwell Plate Assays
- Tangential Flow Filtration System Coupling To Enhance Solution Offerings
- Method Migration Of The USP Ibuprofen Assay And Organic Impurities Method
- Intensifying A mAb Polishing Platform
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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