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| On Demand Webinar | Preventing Costly Out-of-Specification Investigations Out-of-Specification (OOS) investigations in Analytical R&D and QA/QC laboratories are costly and time-consuming. Although analytical instrumentation has seen impressive innovations in speed and efficiency over the last 10 years, sample preparation techniques have remained virtually unchanged for the past 75 years. Sample preparation is now reported to be the most time-consuming, labor-intensive and error-prone part of the workflow, with some 50% of OOS errors attributed to sample processing steps and human error. These OOS errors could be prevented by automation. |
| On Demand Webinar | A unique workflow for linearity testing using automated sample preparation and UHPLC When validating a method according to the ICH guidelines, it is necessary to perform a linearity experiment. This requires the preparation of multiple calibration levels, analysis of the samples by liquid chromatography, and calculation/reporting of the results. Each of these steps can be very time consuming, and in many cases error prone. This is especially true if the analytical method being tested requires the measurement of multiple components. |
| On Demand Webinar | Quick and easy capsule filling for pre-clinical and clinical trials The first step in preparation of pre-clinical and clinical trials is manually weighing in highly potent, hazardous substances precisely with a spatula. This webinar looks at the real practicalities of capsule filling, with a focus on the requirements for use in pre-clinical and clinical phase 0 and 1 trials, and introduces a quick, easy and precise automated solution. |
| On Demand Webinar | Reducing Out-of-Specification Results in QA/QC Weighing out powders to prepare samples and standards for analytical methods such as HPLC can be a time-consuming task with high error risk. With the advent of faster analytical methods, such as UHPLC, and rapid advances in software developments providing faster data processing, attention is once again focussing on sample preparation as the bottleneck in the process. |
| On Demand Webinar | Streamline your powder dosing There are many stages in the drug discovery process where powder dosing is required, in varying target amounts and batch sizes, and into a wide range of different target containers. As new drugs become more effective and more potent, there are also greater risks for the people who are exposed to these compounds during development and formulation. Mettler Toledo’s Quantos automated powder dosing technology has been successfully applied to capsule filling, commercial bottling/filling and QA/QC applications. See how Quantos can improve these processes in terms of quality, productivity and user safety, ultimately saving time and money. |
| On Demand Webinar | Enhancing safety in the workplace: Automated powder dosing of hazardous compounds There is a great awareness within the pharmaceutical industry regarding the hazards involved in handling active drug compounds. One specific hazard is that of exposure to airborne contaminants, encountered during dispensing and handling procedures due to the way in which the analyst works with a balance. Automated powder dosing offers superior protection for the analyst compared to manual dosing. |
| On Demand Webinar | Bottling & Filling of Substances for Commercial Use and Internal Reference In the current global climate, all companies and industries are looking for ways to increase their productivity and reduce their costs. For manufacturers and distributors of fine chemicals, reference materials and standards and particularly those who are concerned with bottling, filling and repackaging of small quantities of chemicals (e.g. 1mg -250mg), there is an automated powder dosing solution that will revolutionise your processes. |
| On Demand Webinar | Good Weighing Practice™ - The Global Weighing Guideline - Part 2: Routine Testing of Weighing Systems Throughout the industry, there are common misconceptions regarding the selection and use of weighing equipment, as well as incorrect testing programs for periodic performance verification. Driven by scientific principles, METTLER TOLEDO has developed Good Weighing Practice™ (GWP®), a risk-based weighing guideline dealing with the entire life cycle of a balance. GWP® provides sound answers to the user's concerns regarding establishing and maintaining sustainable quality of weighing processes. |
| On Demand Webinar | Good Weighing Practice™ - The Global Weighing Guideline - Part 1: Measurement Uncertainty and Minimum Weight Throughout the industry, there are common misconceptions regarding balance selection and use as well as incorrect testing programs for periodic verification of the balance's performance. Driven by scientific principles, METTLER TOLEDO has developed Good Weighing Practice™ (GWP®), a risk-based weighing guideline dealing with the entire life cycle of a balance. GWP® provides sound answers to the user's concerns regarding establishing and maintaining sustainable quality of weighing processes. |