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76 results of "Manufacturing x"
Live Webinar

CAPA: Corrective and Preventative Actions and Non-Conformances

Root Cause Analysis (RCA) is a popular and often-used technique that helps people answer the question of why the problem occurred in the first place. If you only fix the symptoms – what you see on the surface – the problem will almost certainly happen again, w ...

Live Webinar

From Risk Control To Risk Management

This can lead to following regulation to the detriment of managerial principles.: the former aims at keeping averting the most dramatic impacts, whilst the latter helps towards optimizing the risk profile of the enterprise at all times. Such confusion inevitab ...

Live Webinar

Is it Microbiological Method Verification or Validation, or Just Semantics?

This Webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard 17025 for laboratory accreditation in food/water microbiology. Quantitative and Qualitative methods have different ...

Live Webinar

Having Uncomfortable and Awkward Conversations – for HR Professionals

Having difficult and awkward conversations are difficult and awkward for everyone. They can be embarrassing, hurtful, and even relationship ending if not done properly. But they don’t have to be. The ability to handle difficult and awkward conversations is a ...

Live Webinar

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation This highly interactive training uses life examples and explores proven techniques for reducing costs, usually by two-thirds, as ...

Live Webinar

ISO-IEC 17025:2017 Update Introduction: Everything Old is New Again

Many laboratories have successfully developed and implemented a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. Some are still struggling to get accre ...

Live Webinar

Pharmaceutical Compressed Air - Quality GMP Requirements - What you need to know to meet FDA and International Quality Standards

Compressed air for pharmaceutical use is considered a critical utility as many of its applications involve direct contact with the pharmaceutical product. The design, construction and monitoring of a compressed air system is essential for maintaining a quality ...

  • Basic & Intermediate
  • 60 Mins
  • Roger Cowan
  • Nov 23, 2021
Live Webinar

Quality Control of Microbiological Media, Reagents and Test Kits

During this webinar, we will discuss a practical QC approach for in-house prepared and/or commercially purchased media, test kits and reagents specifically applicable to microbiology laboratories to assess the acceptability of the performance of analytical mat ...

Live Webinar

The Secrets to Successful Virtual Teams

Are you working virtually with your team and not sure what to do to make it “click” like all the other teams you hear about? Is working successfully a myth or a fact?It’s a fact! Come learn the secrets of virtual teams so that you can keep them engaged, high ...

Live Webinar

Computer System Validation (CSV) vs. Computer Software Assurance (CSA) as an Approach to Meeting FDA Compliance

As part of the Case for Quality program US FDA CDRH (Center for Devices and Radiological Health) have identified that an excessive focus on compliance rather than quality may divert resources and management attention towards meeting regulatory compliance requi ...