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  • Quick Picks: Spectrophotometers

    Tuesday, October 14, 2025
    Spectrophotometers allow researchers to accurately and reliably quantify concentrations of target compounds, detect and quantify impurities, and observe chemical. typically found in either single or ... read more

  • Quick Picks: HPLC Columns

    Thursday, June 26, 2025
    Liquid chromatography columns use molecule size, polarity, and elution time to separate and analyze target compounds within a given sample. Common column construction includes a stainless-steel ... read more

  • Quick Picks: PCR

    Friday, May 02, 2025
    The polymerase chain reaction, or PCR, is a rapid and cost-effective technique to amplify specific segments of sample DNA. Widely used for diagnostics and screening thanks to its high sensitivity, PCR... read more

  • KIN-TEK FlexStream

    Monday, June 15, 2026
    We have been using this generator for more than 5 years for calibration of instruments. It is easy to operate. Kintek was very helpful in helping to modify cover for easy handling. And they always ...

  • KIN-TEK FlexStream

    Wednesday, May 13, 2026
    We have been using the Flexstream for the past 5 years. It is a high performance instrument that has been operating reliably and up to standard. We use it to generate mixture of gasses at various ...

  • Cary 5000 UV-Vis-NIR Spectrophotometer

    Wednesday, February 25, 2026
    The Cary 5000 UV-Vis-NIR Spectrophotometer is a versatile instrument for optical characterization. It offers superb photometric performance in the 175–3300 nm range and excellent DRA characteristics ...

  • AI in GxP: Annex 11/22, Governance Models & Practical Use Cases

    Join us for this live partner-hosted webinar! AI adoption is accelerating worldwide as organizations assess Annex 11/22 implications, strengthen governance models, and expand digital solutions. This webcast explores how companies are implementing AI responsibly while aligning with global regulatory expectations. Hear practical examples, cross-functional challenges, and lessons learned from early real-world deployments across GxP environments. What You’ll Learn: Annex 11/22 considerations for AI-enabled systems Practical AI use cases across validation, QMS, and manufacturing Governance and oversight models gaining industry momentum Data integrity and traceability risks for algorithmic systems How global regulatory expectations are converging Tools supporting documentation, decision transparency, and control Approaches for cross-functional AI readiness assessments Common pitfalls in early AI adoption Who Should Attend: Quality teams, validation and IT leaders, regulatory specialists, AI governance groups, and anyone preparing to align AI systems with Annex 11/22 and global GxP expectations.

  • Sterility Assurance University

    Sterility Assurance University is the industry’s most focused event dedicated to microbiology, contamination control strategy (CCS), and sterility assurance across the product lifecycle. This two-day summit brings together leading experts from pharma, biopharma, and device organizations to share actionable insights on Annex 1 implementation, environmental monitoring, aseptic processing, and cleaning validation — including lifecycle development, data-driven approaches, and regulatory alignment. Whether you’re preparing for inspections or proactively strengthening your programs, this is your go-to event for expert guidance, peer networking, and practical tools. Top 10 Reasons to Attend Implement a site-wide CCS aligned with Annex 1 and current regulatory expectations Explore environmental monitoring design, trending, and excursion investigations Strengthen your cleaning validation lifecycle from acceptance limits to tech transfer Discover strategies for managing microbial excursions and aseptic process failures Learn from real-world case studies on gowning, airflow, smoke studies, and visual inspection Understand rapid methods, automation, and AI for proactive microbial control Benchmark personnel monitoring and objectionable organism risk assessments Identify design and facility risks that impact contamination control Take home SOPs, checklists, and other takeaway tools you can apply immediately Hear directly from Sanofi, Takeda, Alcon, Charles River Laboratories, and Bausch + Lomb as they share how they’re advancing sterility assurance and contamination control

  • Modernizing Validation for Cloud and Hybrid GxP Systems

    Cloud and hybrid architectures are now central to how GxP systems are deployed, tested, and maintained. This webcast breaks down the evolving expectations for validating these environments as organizations prepare for 2027. Learn how leading teams are balancing risk-based validation, CSA principles, and modern documentation strategies while ensuring traceability, data integrity, and compliance across diverse system landscapes. What You’ll Learn: Validation trends shaping 2026–2027 programs How cloud deployments impact CSV and CSA approaches Strategies for validating hybrid and interconnected systems Where automation and AI assist in documentation and testing Common gaps found in cloud/system validation inspections Data Integrity risks unique to cloud-based platforms Practical templates and approaches for modern validation Frameworks for scaling digital validation efficiently Who Should Attend: CSV/CSA professionals, validation engineers, IT system owners, QA teams, documentation specialists, and teams modernizing systems in cloud or hybrid environments.

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