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The Pharmaceuticals and Biopharmaceuticals industry focuses on the discovery, development, manufacturing, and commercialization of medicinal drugs and biologic products (like vaccines, antibodies, and cell/gene therapies) intended to diagnose, treat, mitigate, or prevent diseases.
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Labs are under pressure to deliver results that are not only accurate but also traceable, defensible, and structured for global compliance.
Technical guide to testing tablets, capsules, and oral dosage forms. Learn methods, regulations, and the role of third-party testing.
Ensure seamless 21 CFR Part 11 compliance for electronic records and signatures in pharma labs. Master FDA regulations, computer validation, and data integrity.
Discover how new FDA guidelines shape Lyme disease drug development and impact clinical care for early erythema migrans cases
Learn how Cytiva’s membranes, filtration systems, and sampling tools help ensure consistent, compliant microbiology testing
Improve precision and reproducibility when working with viscous, volatile, or otherwise difficult liquids
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