FEATURE ARTICLES
Regulations are pushing for an approach to container closure integrity that builds quality into the design and processes rather than testing/inspecting the manufactured item.
- How To Unlock Efficiency In MES Integrations
- Addressing Challenges In Serialization For Complex Therapeutics
- Nitrosamines: New WHO Guidance Provides Expanded Risk Assessment Considerations
- New Initiative Seeks To Back Up ICH's Harmonization Mission
- Quality Imperatives In Oral Solid Dosage Manufacturing: An Overview
- Integrating Quality Processes And Documentation After A Merger
- Improving Governance And Compliance With Knowledge Management
PHARMA ONLINE WHITE PAPERS
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Spray Drying To Enable New Inhaled Drug Products
The formulation and spray drying process can help manufacture a stable, highly respirable powder and deliver products that require a high drug load, a biologic, or rapid onset therapeutic.
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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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Prioritizing Innovation To Get Ahead Of The Market1/10/2023
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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Eliminating Data Integrity Errors Through Digitization10/17/2022
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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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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Simultaneous Spray Drying For Combination Dry Powder Inhaler Formulations7/12/2022
Three combination case studies are demonstrated, in which bevacizumab is paired with erlotinib, cisplatin, or paclitaxel in a dry powder inhaler formulation.
PHARMA ONLINE APP NOTES & CASE STUDIES
- Workflow Solutions: Choosing The Right ITC Binding Experiment
- Analyze Raw Materials to Improve Product Quality
- Standardize Scale-Up And Reduce Time To Market With Mixing Cartridges
- ACQUITY And XBridge Premier Protein SEC 250 Å Columns: A New Benchmark In Inert SEC Column Design
- Optimizing And Intensifying ADC Aggregate Removal With A DoE Approach
NEWSLETTER ARCHIVE
- 05.21.24 -- Addressing Challenges In Serialization For Complex Therapeutics
- 05.20.24 -- Minimize Waste, Maximize Yield And Supor Charge Your Production Process
- 05.20.24 -- Overcoming Bioprocessing Challenges Through A Strategic Tech Transfer Framework
- 05.17.24 -- Discover Solutions For Your Bioprocessing Projects
- 05.17.24 -- Nitrosamines: New WHO Guidance Provides Expanded Risk Assessment Considerations
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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