Quality Control Solutions
-
FlexUP Technology Renewal Program: Keep Your Lab At The Forefront Of Science
4/11/2022
Choose the ideal mix of services with our FlexUP Technology Renewal Program for continuous operation in your laboratory and across your enterprise.
-
Microbial Culture Media For Quality Control Of Non-Sterile Products
4/7/2022
Using the correct media is critical to ensure microbiological quality. Explore a portfolio of culture media and substances for sample preparation, microbial enumeration tests, and tests for specified microorganisms.
-
Benchmark Technology For Filtration-Based Sterility Testing
4/7/2022
Sterility testing is a requirement to confirm that pharmaceutical products purporting to be sterile do not contain viable microorganisms before being released and administered to patients. So, it is vital that the method used for testing medical devices, pharmaceutical products, formulations, tissue materials, and other products is both reliable and accurate.
-
Benchtop Bioprocessing Solutions
Flexible, reliable control and bioreactor systems for laboratory applications
Thermo Scientific™ HyPerforma™ bioprocess control systems are designed to optimize your process from the laboratory bench to full cGMP manufacturing. Our innovative control platform combines a flexible operating system with scalable, modular hardware, novel single-use sensors, and state-of-the-art bioreactors for strategic and streamlined bioprocess control.
HyPerforma benchtop solutions offer robust management of both cell culture and fermentation processes. The open architecture provides process flexibility, and dedicated hardware control allows for expansion. Thermo Scientific™ TruBio™ software is designed to support easy process control and scaling.
-
Comprehensive Batch And Lot Testing Services
7/29/2024
Batch and lot testing for release are critical steps in ensuring the quality and consistency of pharmaceutical tablets. Natoli Scientific provides comprehensive batch testing services that align with stringent industry standards and regulatory requirements. Each lot undergoes a rigorous analysis to verify that it meets predefined specifications for weight, tablet breaking force, thickness, diameter, and dissolution, among other critical quality attributes. The testing process is meticulously designed to screen for any variation that could impact the efficacy or safety of the final product.
Utilizing state-of-the-art analytical equipment and methodologies, our experts ensure that each batch released by our clients is of the highest quality, providing end-users with the assurance that the medications they rely on are both safe and effective. This level of attention to detail fosters trust and reliability in pharmaceutical products processed through Natoli Scientific’s advanced batch and lot testing services.
-
Seal Integrity Inspection Systems with Airborne Ultrasound Technology
7/9/2020
Airborne ultrasound is a referenced technology in the new USP <1207> Chapter Guidance as a deterministic test method for seal quality testing, is an ASTM Test Method F3004 and FDA Recognized Standard for seal quality integrity testing.
-
Microcalorimeters For In-Depth Characterization
5/17/2023
Powerful tools for characterizing protein-protein interactions, structural stability, and formulation compatibility.
-
Discovery Hybrid Rheometers: Temperature Systems And Accessories
4/6/2023
Explore a wide variety of DHR temperature systems and accessories, designed for superior performance and ease-of-use.
-
Powder Rheology Accessory
4/6/2023
The Powder Rheology Accessory expands the DHR’s capabilities to powders, enabling the characterization of behaviors during storage, dispensing, processing, and end-use.
-
Continuous Monitoring Of Cleanrooms And Isolators
1/30/2020
FMS/BioTrak/Portable/Remote/Environmental Sensors