Latest: Eppendorf Launches Innovative New 25mL Conical Tubes
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Eppendorf Launches Innovative New 25mL Conical Tubes
Single-Cell Experiments Reinvented with FluidFM BOT
Simplify QC and Intact Mass Assays with Automated Liquid Handling Solutions
Don’t Overlook Your Incubator: Cell Culture Optimization
Food Process Analytics Comprehensive Guidebook
Near-Infrared Correlation Chart
Controlled, Large-Scale Manufacturing of hiPSC-Derived Cardiomyocytes
Small Scale Perfusion For Cost-Efficient Development of Bioprocesses
A Beginner’s Guide to Bioprocess Modes
Analytical Options for Cannabis Testing
Hematology Analyzers & Stainers
Clinical Chemistry Analyzers
Flow Cytometry for Screening
Pre-Clinical and Clinical Lab Automation
SLAS Europe 2019 Conference...
26 Jun 19 - 28 Jun 19
04 Aug 19 - 08 Aug 19
30 Oct 19 - 31 Oct 19
To meet the specific challenges of biopharmaceutical development, we have a team of scientists with expertise in immuochemistry and cell based approaches for this important class of therapeutic agent. Read more...
As regulatory pressure increases on pharmaceutical companies to investigate the potential interaction between a dosage form and the components of the primary closure and transfer system employed, leachables and extractables studies are b... Read more...
Within the pharmaceutical sector, there is an increasing regulatory requirement for the characterisation and counting of visible and sub-visible foreign particles in pharmaceutical products from a safety, quality and efficacy perspective. Read more...
Handling, processability and performance of a material are dictated by its bulk physical properties. At LGC, we believe that characterisation and accurate measurement of crucial material attributes are an essential part of product developm... Read more...
ProBioGen holds a manufacturing authorization for GMP (Good manufacturing practice) compliant manufacturing and batch release of biotechnological drug substances and fulfills all present regulatory requirements by EMA and FDA.
GMP Man... Read more...
Ready 4 Action, proprietary feasibility assessment, sets the cornerstone of a cost-effective product development plan.
Ready 4 Action is the four-step process used to evaluate the viability of proposed drug products. This important to... Read more...
Camargo ensures the appropriate regulatory requirements are met every step of the way, streamlining your drug development process all the way to approval. Ready to guide you through the preclinical stage of drug development, Camargo pr... Read more...
Superior Regulatory Service Helps Transform Your Clinical Trials.
Strong regulatory strategies are pivotal in getting products to market. While many countries’ drug regulations are similar, there are still significant differences. The... Read more...