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Webinars

 

29 May 2019 SUEZ

Don’t let difficult substances control your cleaning validation

29 May 2019 | 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...

ON-DEMAND

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...

ON-DEMAND

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…

ON-DEMAND

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...

ON-DEMAND

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…

ON-DEMAND

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…

ON-DEMAND SUEZ HERO IMAGE

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…

ON-DEMAND Bruker Webinar

Quality assessment of biologics: higher order structure analysis using NMR

ON-DEMAND | By Bruker

The webinar describes how 2D NMR can offer protein biochemists unprecedented analytical precision. By assigning just one spectrum, users can obtain a unique fingerprint of a protein at an atomistic resolution. This non-destructive technique can also be combined with other complimentary techniques to gain even further insights into sample quality.…

ON-DEMAND

Creating a connected ecosystem to gain insights across R&D

ON-DEMAND | By Thermo Fisher Scientific

This webinar will address some of the challenges faced by regulated and non-regulated labs as they move to cloud technology, the importance of implementing an extensible lab informatics platform solution and how digital technology has the potential to change how science is performed...