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Featured Whitepaper: Vaisala
Understand the Highest Risk Parameter: Download the Humidity Toolkit
Sponsored By: Vaisala
Humidity is the hardest variable to measure accurately in any controlled environment, but we can help. Download these three tools: the Humidity Calculator, the Humidity Conversions booklet, and the Vaisala Calibration Handbook. The calculator works online or offline, and with any mobile device. |
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Vcaps® Plus HPMC Capsules for Pharmaceutical Dosage Forms
Author: Dominique Cadé
Sponsored By: Capsugel
Vcaps® Plus capsules developed without gelling agents provide HPMC capsules with improved physical and operational features to match the needs of the pharmaceutical industry. |
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Protecting Workers from Skin Allergies White Paper
Sponsored By: Ansell Occasionally wearing glove products can cause issues with our health. This predominantly manifests itself in the form of allergic reactions and contact dermatitis. This paper reviews these various allergies and their causes, and discusses the glove solutions that are available. |
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Using Isolators for ADC Production
Author: Gary Partington
Sponsored By: Walker Barrier Systems This paper will discuss the use of isolators for the production of antibody drug conjugates providing operator protection during API preparation and providing product protection during final filling. |
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Fermentation Technology and Contract/Toll Manufacturing at AbbVie
Sponsored By: AbbVie
Abbvie Contract Manufacturing has extensive experience and capacity across a wide variety of organisms including Streptomycetes, Actinomycetes, yeast, fungal, E. coli, and Bacillus. Our expertise also includes fermentation with genetically modified organisms. AbbVie is also a multi-product approval facility and can manufacture products for a wide variety of industries including pharmaceutical, agricultural food, nutriceutical, enzymes, and chemical. |
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Best Practices for FDA Compliance Solutions
Author: Brenda Percy Sponsored By: EtQ, Inc.
Learn some key elements to spotting a good FDA compliance solution, techniques for achieving GMP compliance, and how to ensure that quality and compliance are met in the Life Science industry. |
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Amino Acid Analysis According to Ph.Eur 2.2.56
Author: Benjamin Rietschel
Sponsored By: SGS Life Science Services
Employing spectrophotometry and liquid chromatography quantitation of Ninhydrin-positive substances achieves 0.05% reporting sensitivity, required by the updated Ph. Eur. 2.2.56. This white paper details our results compliant with the new monographs. |
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Cleaning Validation for Pharmaceutical Manufacturing
Author: Malcolm McLaughlin
Sponsored By: Alconox Inc.
This paper outlines the basics of cleaning validation, as well as discusses the kinds of support services needed for critical cleaning products in order to optimize your cleaning validation process. |
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