How to avoid the next nitrosamine crisis: 5 lessons learned about impurity detection

Learn more about differentiating between quality risks and data errors, and how to best ensure the quality of your products in this upcoming webinar

28 Feb 2020
Finn Price
Administrator / Office Personnel

Expert insights

When a crisis occurs, hindsight is a great teacher. Any company creating products that impact human health can learn from the recent nitrosamine contamination of heart drugs by looking at their own quality processes for anything that could result in a similar contamination issue. Analytical data should have been able to support confidence in the quality of manufacturing and did in fact first identify the presence of nitrosamines, but not before the contamination had spread.

In this SelectScience webinar, Heather Longden of Waters Corporation, will discuss key analytical tests, how to improve methods and gain more information about your samples and how Waters analytical expertise can help your scientists and chemists support the quality of your products, be they food, cosmetics, or drugs.

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Key learning objectives:

  • Key analytical tests that might be overlooked
  • Enhancing analytical tests to get more information about your samples
  • Improving analytical methods in regulated environments
  • Leveraging automation to minimize manual intervention and detailed review requirements
  • Using scientific review to look for quality risks rather than data errors

Who should attend?

  • Lab Managers
  • Lab Directors
  • Quality Teams
  • Quality Leaders

The live webinar takes place on Wednesday, March 11, 2020, at:

  • 16:00 GMT
  • 12:00 EDT
  • 09:00 PDT
  • 17:00 CET

Scheduling conflict? No matter, register to receive an on-demand link to watch later>>

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RegulatoryPharmaceutical regulations impact on all areas of drug development, manufacture and control and supply. Services are provided from the early stages of drug development and clinical trials through to dossier submission, approval and marketing. Regulatory also includes submission of analytical studies from the pharmaceutical product and safety. Quality ControlQuality control is needed in all production processes. Quality control is a monitoring procedure or set of procedures that are put in place to ensure that a manufactured product adheres to a defined set of quality criteria. AutomationAutomation in laboratories and manufacturing processes enhances efficiency, precision, and scalability by reducing the need for manual intervention. It plays a critical role in improving productivity, minimizing human error, and accelerating workflows in fields like diagnostics, drug development, and industrial testing. Automation technologies include robotic systems, automated liquid handlers, and process control systems that streamline complex tasks and ensure consistent, reproducible results. Explore our peer-reviewed product directory to discover the best automation solutions, compare options, read user reviews, and get prices directly from manufacturers.PharmaceuticalsPharmaceuticals are medicinal drugs used in healthcare to diagnose, prevent, cure and treat illnesses. Pharmaceuticals that are excreted after use appear in wastewater and can have detrimental effects on the environment.