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Limit ultrapure water system costs and downtime using Ozonia ozone technology

19 November 2019 By SUEZ – Ozonia® Ozone Systems

The goal of this webinar is to familiarize companies with the applications and benefits of ozone technology in ultrapure water systems and Ozonia Membrel® electrolytic technology – SUEZ’s ozone product that produces ozone directly from water instead of gaseous air or oxygen.

Accelerate food, pharmaceutical and particle analysis with Raman imaging

22 October 2019 By WITec GmbH

This webinar will describe how Raman microscopy can help solve some of the most vital and challenging questions that researchers face in 3D imaging and microparticle analyses of food, pharmaceuticals and microplastics, along with providing measurement examples from each field.

Don’t let difficult substances control your cleaning validation

ON-DEMAND By SUEZ

TOC analysis is a widely adopted method for detecting residual product or cleaning agents on manufacturing equipment. Compared to specific methods such as HPLC, TOC can provide better process understanding and efficiency for cleaning validation (CV), verification and continuous monitoring...

Integrated pharma manufacturing – It works

ON-DEMAND By ACG

This webinar focuses on the benefits of integrated pharma manufacturing using examples of integrated processing and packaging solutions. The webinar will also highlight the key advantages of choosing a single pharma solutions provider for all manufacturing needs...

Improve ultrapure water system performance and uptime with ozone

ON-DEMAND By SUEZ – Ozonia® Ozone Systems

Securing water quality in pharmaceutical manufacturing operations is essential to protecting product quality. One tool that continuously protects water loops is ozone technology. This webinar is designed to help companies understand the application and benefit of ozone technology in ultrapure water systems and how ozone solutions can improve water system…

Take control of your impurities testing

ON-DEMAND By PerkinElmer

The control of impurities plays a crucial role in Pharma QA/QC and can be divided in 3 main buckets: Organic, Inorganic and Residual Solvents.  On this webinar we are focusing on analytical techniques used for control of Inorganic impurities and Residual Solvents...

Understanding the complexities of global serialisation & traceability regulations

ON-DEMAND By Clarivate Analytics

In 2017 the WHO estimated that the counterfeit drug market represents around 10-15 per cent of the pharmaceutical market worldwide, with an estimated $200bn revenue per year. Worldwide there were 3,509 pharmaceutical crime incidents in 2017, which represents an 11% increase from 2016. Most falsified medicines that reach the market…

Advances in automated performance verification for UV/VIS spectrophotometers

ON-DEMAND By Mettler-Toledo

Regulated environments require performance verification (qualification) of UV/VIS spectrophotometers on a regular basis. Instrument performance is the main factor directly affecting the accuracy and repeatability of measurements. Hence, it is important that this is regularly monitored and that documentary evidence is provided. Optical performance verification is conducted to the widely…

Understanding current CFR 21.11 and data integrity requirements

ON-DEMAND By SUEZ

The US FDA and European Commission have defined regulations relating to the submission of electronic records in lieu of paper documents, for submission, inspection, and archiving purposes. When ageing analytical equipment is to be replaced 21CFR Part 11 and EU Annex 11 are also topics of discussion. Common questions from…