UV7 UV/Vis Spectrophotometer
Ideal for regulated environments, the UV7 complies with the strict Pharmacopeia regulations and supports 21 CFR Part 11 data integrity compliance with the additional LabX Software.
UV7 UV/Vis Spectrophotometer
Automated UV/Vis performance verification according to Pharm
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Excellence Performance
FastTrackTM technology ensures exceptional optical performance. Automated performance verification is possible with the optional CertiRefTM module.
Simple One ClickTM Operation
The large color touchscreen features an intuitive One Click interface. All users have their own home screen, enabling daily tasks in just One Click.
Measurements Within Seconds
Comprises modern fiber optics in combination with CCD array detection and a Xenon flash lamp. A full spectrum scan in performed within just 1 second.
Automated Performance Verification
With regular UV Vis performance verification, you can always be sure that your instrument is working properly and that your results are accurate and reliable. The performance verification tests are US and European Pharmacopeia compliant and include, among other tests, photometric accuracy, photometric linearity, wavelength accuracy, resolution and stray light. The plug and play modules are easily installed within seconds.
Relevant applications:
• Pharmaceutical
• Quality control and quality assurance
• Chemical
• Academia
• Cosmetics
• Petrochemical
Brochures
Seamless lab compliance for pharmaceutical manufacturers
The pharmaceutical industry is highly regulated, with standards and regulations such as good manufacturing practice becoming increasingly important. METTER TOLEDO provides an overview of the regulatory landscape related to analytical and weighing processes in pharmaceutical labs, and recommends solutions that meet standards and support compliance. The guide also highlights how the pharmaceutical industry can utilize state-of-the-art products incorporating high-tech functions and clever design details to ensure regulatory compliance throughout the entire product lifecycle.
Pharmaceutical quality control ensuring excellence and compliance
Pharmaceutical laboratories navigate rigorous guidelines and must maintain exhaustive documentation to ensure public health and meet regulatory compliance. Inefficient quality control can lead to significant operational setbacks, including product release delays, increased storage costs, regulatory penalties, and production bottlenecks.
Explore how modernized practices such as automation, data integrity, analytical service, quality control, and the importance of service and training are crucial for maintaining accuracy, efficiency, and compliance of pharmaceutical operations.
Additionally, learn about the advancements in personalized medicine and the enabling technologies that are shaping its development.
