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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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Found a foreign object in the production line? Employ forensic failure analysis to isolate the root cause, satisfy cGMP CAPA requirements, and safely resume operations
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
Join us and Thermo Fisher's Suja Sukumaran, PhD, to know how FTIR spectroscopy supports material identification, product testing, and regulatory compliance across industries
How to test, certify, and compliantly dispose of surplus laboratory assets — covering safety verification, regulatory requirements, and sustainable disposition
Labs that invest in junior and mid-level staff build broader organizational competency, reducing dependence on specific individuals
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
Join us and Waters' Duanduan Han, PhD, to explore how LC-UV/MS workflow can help labs meet safety and regulatory standards for GLP-1 analogs
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
Learn the phases, STAT vs. routine benchmarks, what affects TAT in contract testing, and how to specify TAT requirements when outsourcing lab work
Discover the critical role of Shilajit purity testing in safeguarding consumer health, enhancing product credibility, and navigating global regulatory landscapes.
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?
Integrating third-party laboratory testing into procurement process transforms unknown supply chain risks into defensible, data-backed certainty
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
Gummies are unstable. Are you overdosing your product just to meet label claims at expiry? There is a smarter way to test.
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
Watch your favorite or all the webinars from the virtual event on demand for free
Register today to attend the 2025 Outsource! Week for Lori's session on efficient sample storage and management along with other insightful talks
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
Stay ahead with data-intensive, digitally connected, and regulation-driven clinical testing lab operations
Register today to access these curated webinars live or on demand
Investing in early phase potency assays and RMMs and aligning with GMP modernization can future-proof pharma testing labs
Global compliance depends on precise, reproducible chemistry testing built on accredited analytical methods
Labs are under pressure to deliver results that are not only accurate but also traceable, defensible, and structured for global compliance.
Is your lab prepared for the next wave of regulatory, technological, and client-driven changes?
Expert sample management can bring in new therapies and devices into the market sooner and ensure they remain accessible and affordable
Here's how third-party labs verify supplement safety, potency, and label accuracy under US regulations
Potency testing ensures biopharmaceuticals are safe and effective. Find out how contract labs deliver validated assays and 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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