Infographics
Redefining value in drug development and clinical research
The Tufts Center for the Study of Drug Development, a nonprofit research group affiliated with Tufts University School of Medicine, analyzed the financial and operational impact of aligning manufacturing, clinical research, laboratory, and supply chain services under a single provider.
Exploring the Frontier of Organoid Characterization
In the quest to understand human biology at a deeper level, organoids have emerged as a groundbreaking tool, offering a three-dimensional (3D), miniature representation of human organs.
Ten Steps That Risk Failure in Temperature-Controlled Clinical Supply Chains
This infographic highlights the most common risk points in temperature-controlled clinical supply chains that can jeopardize product integrity.
Boost Productivity in mAb Capture Chromatography
Develop a Protein A Step That Matches Your Needs
Accelerate time to market with integrated CDMO and CRO services
A Contract Development and Manufacturing Organization (CDMO) supports sponsors at every stage of drug development, from early research and development to clinical trials through to commercialization.
Sustainable Weighing for a Greener Lab: Discover the Quintix® Pro Standard Balance
Reduce environmental impact while achieving precision in lab weighing. Learn how sustainable design, energy efficiency, and responsible sourcing set the new standard for analytical balances.
Revolutionizing Single-Use Systems for Biopharma
Ami Polymer’s Single-Use Systems (SUS) are designed to enhance efficiency, sterility, and compliance in biopharma processing. With an ISO 7 certified cleanroom and an end-to-end validated manufacturing process, our solutions ensure reliability at every stage of your workflow.
Pipetting Compliance ISO 8655:2022 Part 10
In 2024, ISO 8655:2022 was expanded to include a new Part 10, providing essential guidelines for setting up an ISO-compliant laboratory environment. Learn how these updates affect your pipetting workflows.
Ensure Pipetting Accuracy & Compliance with ISO 8655:2022 Part 10
The latest updates in ISO 8655:2022 Part 10 provide essential guidelines to enhance pipetting accuracy, compliance, and efficiency. This comprehensive resource will help you.
9 ways to ensure a reliable technology transfer
Technology transfer is a vital process in the pharma industry, crucial for scaling up drug production, relocating to a new facility, or transitioning to a new outsourcing partner.
