Welcome to your one-stop resource for pharma-regulated quality control testing. Here, we provide a wealth of information and resources designed to support professionals in the pharmaceutical industry. From the most recent advancements in quality control testing to in-depth guides and tools, we are committed to helping you maintain the highest standards of quality and safety in pharmaceutical production.
Learn about ensuring safety in biologics production, preventing and eliminating mycoplasma contamination, and microbial limits testing
Biocontamination Control Strategy: FDA insights, cleanroom tips, and barrier tech
Using Microsart® @filter
Download this poster to learn how to prevent mycoplasma contamination and spread in your cell culture lab.
Learn five tips for preventing mycoplasma contamination in the cell cultures in this easy-to-understand infographic.
Understand how real-time PCR can be implemented as sterility testing method for ATMPs
Learn how the Microsart®@filter PVDF is a robust solution that ensures effective recovery of microorganisms after filtration of various disinfectants.
How to Achieve Pharmacopeia-Compliant Bioburden Testing of Viscous Samples
A PCR Kit Manufacturer Perspective
Download the application note and discover more about the influence of incubation conditions on microbial recovery on R2A Agar
Optimizing microbial enumeration in viscous substances is critical. This study explores how temperature & dilution with IPM impacts, using Microsa...
This infographic covers continuous air monitoring, isokinetic sampling and advantages of gelatine filters
This application note presents a benchmark study comparing the capabilities of two different qPCR kits for the detection of Mycoplasma.
Be prepared for Annex 1 and EN17141 regulations and download our application note.
In this study, we evaluated the Sterisart® closed system sterility testing device, with a septum, for the recurrent sterile extraction of samples.
Discover Sartorius solutions for Microbiological QC throughout the biopharma production process, from process development to final release.
This interactive PDF/playbook helps you to easily identify the right sterility testing canister for your application. The playbook also provides an ov...
In this poster, a validation study was designed to evaluate bacterial and fungal detection capability.
Discover expert insights into the BLI technology that's revolutionizing quality control in the biopharmaceutical industry.
Discover how a single analyte concentration can be used to accelerate biosimilar development when using an Octet® BLI system.
Learn how the high-through-put Octet instruments and reagents can be used to design assays that rapidly characterize multiple attributes of antibody b...
Novel, High-Throughput Approach for Testing Development Samples
Discover how Octet® BLI systems revolutionize quality control (QC) testing for increased efficiency, productivity, and compliance.
Up to 2x faster and with the ability to process 40x more samples per day, Octet BLI technology is an ideal replacement for ELISA, SPR, and HPLC
Octet® GxP packages support the GMP compliant implementation, including 21 CFR Part 11 software, validation packages, and biosensor validation support...
For Process Development and Quality Control
A method for evaluating the binding of an Fc gamma receptor III (FcγR) molecule to the widely characterized NIST mAb.
Rapid, accurate and cost-effective quantitation of monoclonal antibodies (MAbs) is essential for bioprocessing.
Collection of technical documentation to effectively limit interferences.
Contamination Under Control for Reproducible Amplification
Collection of technical documentation for safe cultures and minimal variances
Ergonomic Preparation to Prevent Cross-Contamination
Lab essentials for tailored sample preparation
Streamline routine CLD tasks, achieve more accurate results, avoid contamination, and simplify workflows.
Download this infographic to learn four ways to immediately improve the quality of your samples for common QC assays.
Explore what type of ultrapure water is suitable for use in endotoxin analysis and how to validate and verify it is endotoxin-free.
HPLC is an analytical procedure for separation, identification and quantification of substances using liquid chromatography.
On Recovery and Adsorption of Various Therapeutic Proteins at Low Sample Volumes
Are you following methods for current Good Laboratory Practice (cGLP) or current Good Manufacturing Practice (cGMP)?
See how Sartorius Minisart® PP filters reliably remove particles from your samples without adding unwanted extractables or leachables.
Digitalization is a key success factor in today's labs, increasing data accuracy and improving the efficiency of research and analysis. Explore the cr...
This infographic provides an overview of key terms and definitions, points of compliance, and ways to achieve quality control and data integrity.
Master precision by exploring the implications of the ISO 8655:2022 standard, its most important changes and their impact on pipette users.
Our series of Generic Operating Procedures provides valuable information about routine testing of lab balances. Discover more!
Discover practical guidance on weighing in the lab, including calibration, accreditation, legal metrology and correct weighing.
Our white paper summarizes USP Chapters <41> and <1251> and the new European Pharmacopoeia Chapter 2.1.7.
Ensure compliance with the updated European Pharmacopoeia guidelines and how the Cubis® II laboratory balance supports this.
Generic operating procedure for a performance test according to chapter <41> of the United States Pharmacopeia (USP).
The recent pandemic demonstrated the need for rapid and safe global vaccine production. Explore the key points of vaccine quality control!
In cell culture-based vaccine manufacturing processes, microbial contamination control and impurity testing are crucial elements of quality control.
Get QC Results for Advanced Therapy Medicinal Products (ATMPs) Before Treatment
Discover the most important techniques used for the characterization of drug products, the parameters to be considered during lab balances qualificati...
Innovative QC instruments and consumables for microbiological, physicochemical, and biological analyses, supporting accurate and reliable results.
A high-performance balance that will align with your unique demands and compliance requirements.
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