Annex 1 Revisions: Let’s talk TOC and conductivity requirements for pharmaceutical water systems
ON-DEMAND By SUEZ
Register for our latest webinar on the proposed Annex 1 revision on pharmaceutical water to prepare for future compliance...
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Webinars
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…
Compliance with data integrity and computerised system validations
ON-DEMAND By PerkinElmer
During this webinar, we will investigate trends seen globally for data integrity violations and avenues for remediation...
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 percent 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 do…
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…
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.…
Overcoming unusual challenges in the characterisation of a monoclonal antibodies by LC-MS from early to late stage of development
ON-DEMAND By SCIEX
Different modalities of monoclonal antibodies are pushing the limits of characterization by MS: new critical quality attributes need to be carefully monitored from developability in early phases and then during process development and clinical phases...
Navigating data management challenges in the pharmaceutical life cycle
ON-DEMAND By Abbott Informatics
In this webinar, we’ll introduce you to laboratory information management systems (LIMS) and demonstrate how this software can help you achieve regulatory compliance, quality data management throughout your product’s lifecycle...
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...
Validating a rapid method for pharmaceutical applications
ON-DEMAND By BD Diagnostics
This webinar discussed how the validation of rapid methods continues to be an obstacle to greater adoption of these technologies.
Leveraging cutting-edge Rapid Microbiological Methods to gain a comprehensive understanding of your environment and a competitive advantage
ON-DEMAND By Abzil BioVigilant
This webinar offers insight from both an end user and a supplier in order to share with you compelling reasons to consider the use of RMMs to gain a better understanding of your environment while improving your competitive advantage...
ISO/IEC 17025:2017 – New definitions for specifications, decision rules & risk assessments for calibrations
ON-DEMAND By Vaisala
The 2017 revision to ISO/IEC 17025 includes better guidance on conformity and a new risk-based approach. In this webinar we discuss the revision in terms of temperature and humidity calibration in life science environments...
