Pharmaceutical Analysis

What You Need to Know about Computerized System Validation: GAMP 5 2nd Edition

This webinar takes a look at the contents of the long awaited GAMP®5 Version 2 release to examine what has truly changed since the Version 1 release, with special focus on what might impact regulated laboratories in the pharma, biopharma, and...

Understanding of USP<1058> updates and insights in regulations

Learn about how USP <1058> aligns with GAMP® 5, the core elements of the <1058> instrument life-cycle framework, and areas of <1058> the USP are exploring improvements in by attending this upcoming webinar.

Regulatory Challenges in Pharma 4.0

In this forum, the expert panel discuss acceptance from regulators on new technology, and other key issues regarding Pharma 4.0. 

Impact of COVID on Pharma 4.0

In this forum, the expert panel discuss changes to the pharmaceutical manufacturing processes during and post the COVID pandemic including what technologies have been adopted to increase speed and efficiencies. 

Trace Level Impurities in Pharmaceuticals

This virtual forum discusses the risk assessment and analytical challenges of detection and quantification of trace level impurities in pharmaceutical products including mutagenic nitrosamine impurities.

PolyAnalysis Forum on Complex Polymers

The second event of the PolyAnalysis Forum series will focus on new polymers with complex architectures. Join the presenters on December 2, 2021 for this virtual event with live Q&A.

Pharma 4.0: Analytical Procedure Lifecycle Management

In this forum, the expert panel will discuss applying an enhanced approach to the lifecycle of analytical procedures from development through validation, transfer, operational execution, and change control until final discontinuation.

The Importance of Data Integrity in Achieving Pharma 4.0

This on-demand webinar explores why organizations cannot continue to advance with only technology and must also understand the evolution of data integrity. For further details and to register, click below.

[Webinar] Analytical Methodologies for Nitrosamines: Challenges and Solutions

This on-demand webinar presents a case study of risk assessment implementation and covers analytical methodologies for N-nitrosamines with their challenges and suggested solutions. By watching this presentation you will: 1) Get background...

Continuous Manufacturing: Business Case Drivers, Control and Deployment Strategies for Small Molecule Oral Products

With the move from traditional batch manufacturing to continuous manufacturing there is a need for real-time monitoring and real-time release of products - learn more from Janssen Pharmaceuticals.

[Webinar] How Can LIMS Deliver Value to Your Pharma Manufacturing Lab?

Separation Science, in collaboration with Thermo Fisher Scientific - Digital Science, offers a webinar focusing on how laboratory information management systems (LIMS) can deliver value and efficiency, and increase productivity, in your...

How to Select a Reproducible Starting Point in HPLC Method Development

Separation Science, in collaboration with Phenomenex offers an on-demand webinar 'HPLC/UHPLC Reversed-Phase Method Development: Selecting a Reproducible Starting Point' with pharma industry expert, Dr Phil Koerner.

Methods and Applications to Improve Pharmaceutical Workflows

Benefit from a series of educational resources aimed at pharmaceutical scientists, ranging from pharmaceutical impurity method development, to a complete HPLC workflow comprising multiple detectors, to strategies to improve productivity and reduce...

Easy characterisation workflows in therapeutic protein analysis

Looking for new and improved technologies to advance your peptide mapping strategies? Do you want to overcome automation problems with your therapeutic protein workflows? If so, signup for this educational presentation...

Get more information in less time: Improve your peptide mapping and PTM analysis skills

Peptide mapping is critical for characterizing protein drugs and monitoring product critical quality attributes (CQAs) in biopharma. Due to the heterogenous nature of protein drugs, comprehensive analytical characterization is required for getting...

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