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Pharmacology & Drug Development Testing encompasses studies to understand how drug candidates interact with biological systems and to assess their safety and efficacy before they can become approved medicines.
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Explore the essential analytical and microbiological laboratory tests to ensure your diluents meet strict USP monographs
Preclinical data is commercially useful only when it adheres to stringent global quality management frameworks
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From LADME frameworks to toxicokinetics, discover why PK/PD testing is the critical bridge between preclinical discovery and clinical trial success
Join us and Thermo Fisher's Suja Sukumaran, PhD, to know how FTIR spectroscopy supports material identification, product testing, and regulatory compliance across industries
With global supply chains expanding for repurposed anthelmintic APIs, robust third-party testing is essential to verify compound identity, ensure potency, and maintain strict regulatory compliance
By understanding and implementing effective raw material testing methods, the pharmaceutical industry can continue to deliver high-quality, safe medications to patients worldwide.
Ensuring Quality and Efficacy for Ozempic and Wegovy
Ensuring Safety and Efficacy in Diabetes and Weight Loss Treatment
Psilocybin potency testing is an essential step in ensuring the safety, quality, and efficacy of psilocybin products.
Researchers, developers, and manufacturers should be able to leverage the unique advantages of both small and large molecule approaches to address unmet medical needs
What are the exact testing protocols compounding pharmacies need to confidently release weight-loss injectables? How to find the right contract lab to run them?
Explore how lab service providers are using smart technology and digital evidence to adapt to stricter global regulations
Manual data translation limits AI, but connecting the DMTA cycle turns scattered data into actionable knowledge
From PFAS to supply chain compliance, 2025 tested how contract laboratories really adapted
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Biosimilars represent a promising opportunity to enhance healthcare affordability and accessibility by providing alternatives to costly biologic therapies.
Despite the traditional critique, the industry strictly regulates the dietary supplements entering the market
Join Michael's talk at the 2025 Outsource! Week for tips on how to decide if method validation or verification suits your product
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Investing in early phase potency assays and RMMs and aligning with GMP modernization can future-proof pharma testing labs
Labs are under pressure to deliver results that are not only accurate but also traceable, defensible, and structured for global compliance.
Expert sample management can bring in new therapies and devices into the market sooner and ensure they remain accessible and affordable
How contract labs support compounding pharmacies with sterility, potency, and compliance testing under USP <797>
Potency testing ensures biopharmaceuticals are safe and effective. Find out how contract labs deliver validated assays and global compliance
A comprehensive overview of the 21st Century Cures Act for healthcare and research professionals, detailing its impact on innovation and patient care
Technical guide to testing tablets, capsules, and oral dosage forms. Learn methods, regulations, and the role of third-party testing.
Encapsulate success: Explore liposome research, characterization, stability, and safety testing for advanced drug delivery. Find expert labs for your needs.
Discover how new FDA guidelines shape Lyme disease drug development and impact clinical care for early erythema migrans cases
Master RCA in Pharma QA to identify root causes, prevent recurrences, and enhance quality. Essential for compliance and patient safety
Master ICH Q3D elemental impurities testing in pharma. Ensure safety, compliance & quality. Expert lab services for accurate analysis & risk assessment
Understand the comprehensive role third-party laboratories play in enhancing accuracy, credibility, and innovation in controlled substance testing
As regulatory bodies like the FDA and USP continue to emphasize method validation and bioequivalence, laboratories must ensure their dissolution testing practices are scientifically sound and regulatory compliant.
Rigorous analytical testing ensures that APIs meet the highest standards for identity, purity, potency, and stability—safeguarding patient health and maintaining market confidence.
Advanced automation and high-throughput screening for contract testing labs
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