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Biology & Life Sciences Testing encompasses a broad range of analytical services for biological systems and products derived from them.
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A landmark FDA direct final rule officially clears the path for organs-on-chips and in vitro models. Advanced CROs can capture the shifting outsourcing market
Analytical testing is now the primary bottleneck in GLP-1 manufacturing. Strategic lab qualification prevents batch stalls and protects revenue
Register today to access these curated webinars live, or on demand, and interact with our industry experts directly
This full-spectrum synthesis expansion addresses the scale-up gap in MRD and MCED programs
Untargeted LC-MS metabolomics with computational quantitation, without per-analyte calibration
With the 2026 Cyclospora outbreak linked to fresh lettuce, learn why this parasite evades traditional swabs and how FDA molecular testing can secure your produce supply chain
Learn why regulatory bodies shifted from PFGE to WGS—and how outsourcing to an accredited contract lab can accelerate contamination investigations
Explore modern pathogen detection technologies, FDA traceability mandates, and the shift to rapid food safety
Explore the essential analytical and microbiological laboratory tests to ensure your diluents meet strict USP monographs
Partner with this California-based FDA-registered contract lab for deformulation and advanced GC-MS/NMR chemical analyses
Preclinical data is commercially useful only when it adheres to stringent global quality management frameworks
Register to watch all the webinars at your convenience, now available on demand
From LADME frameworks to toxicokinetics, discover why PK/PD testing is the critical bridge between preclinical discovery and clinical trial success
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
Attendees can connect directly with our expert speakers in the Q&A segment post each session
Psilocybin potency testing is an essential step in ensuring the safety, quality, and efficacy of psilocybin products.
Learn the phases, STAT vs. routine benchmarks, what affects TAT in contract testing, and how to specify TAT requirements when outsourcing lab work
While BART has some limitations, its benefits make it a valuable addition to water management and environmental testing industry
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?
Manual data translation limits AI, but connecting the DMTA cycle turns scattered data into actionable knowledge
Regulators are watching: Ensure your cultivated meat is free from growth factor residues before it hits the shelves.
From PFAS to supply chain compliance, 2025 tested how contract laboratories really adapted
Regulatory signals, audit expectations, and testing priorities labs should be preparing for as 2026 approaches
Register today to attend the 2025 Outsource! Week for Lori's session on efficient sample storage and management along with other insightful talks
Biosimilars represent a promising opportunity to enhance healthcare affordability and accessibility by providing alternatives to costly biologic therapies.
Introduction: The Challenge of Biologic Therapeutics Biologics—therapeutic products derived...
Anthrax bacteria testing is crucial to detect, prevent, and manage outbreaks, ensuring public health safety
Join Michael's talk at the 2025 Outsource! Week for tips on how to decide if method validation or verification suits your product
Stay ahead with data-intensive, digitally connected, and regulation-driven clinical testing lab operations
Investing in early phase potency assays and RMMs and aligning with GMP modernization can future-proof pharma testing labs
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