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325 results of "Life Sciences x"
Live Webinar

Creating Optimal Sampling Plans

A sampling plan is a term widely used in research studies that provide an outline of the basis on which of research is conducted. It tells which category is to be surveyed, what should be the sample size and how the respondents should be chosen out of the popu ...

Live Webinar

The Transfer of Validated Methods

This webinar will discuss the best practices for the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.

  • Basic & Intermediate
  • 60 Mins
  • John Fetzer
  • Dec 05, 2022
Live Webinar

Outsourcing Software Development for Medical Devices

This webinar will discuss the skillsets to look for when outsourcing, how to know if the work is compliant (without having to be an expert in software development), how to manage outsourced development, and your responsibilities throughout the product lifecycl ...

Live Webinar

Bulletproof CAPA Process: How to do it Right?

FDA, EU Notified Bodies, and other regulatory authorities investigate the capability of organizations to identify processes that require corrective and preventive actions. Organizations should provide evidence that they have the required means and abilities t ...

Live Webinar

The 6 Most Common Problems in FDA Software Validation and Verification

This training on FDA software validation and verification will provide you with the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.

Live Webinar

HPLC Analytical Method Development and Validation

Instrumental liquid chromatography is an analysis widely used to determine purity, impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of ...

  • Basic & Intermediate
  • 60 Mins
  • John Fetzer
  • Dec 19, 2022
Live Webinar

How to Deal with Bad Results Under GLP

Assessment of the cause for non-compliance is a structured series of branching questions. The answers to these eliminate possibilities and eventually highlight a root cause. This process is described, including roles and responsibilities, timing, and efforts a ...

  • Basic & Intermediate
  • 60 Mins
  • John Fetzer
  • Jan 04, 2023
Live Webinar

Computer System Validation (CSV) for FDA-Regulated Computers

The Webinar will focus on the importance of ensuring that the validation of an FDA-regulated computer system will meet compliance guidelines. This includes the development of a company philosophy and approach and incorporating it into an overall computer syst ...

Live Webinar

The 11 Must-Have Documents Of software Verification and Validation

The verification and validation of medical industry software are coming under increased scrutiny by the U.S. FDA. This webinar will address the use of the FDA, GAMP®, 21 CFR 11, and other applicable industry software validation models, coupled with the ISO 14 ...

Live Webinar

Analytical Method Validation Under Good Laboratory Practices - GLPs

If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof t ...

  • Basic & Intermediate
  • 60 Mins
  • John Fetzer
  • Jan 18, 2023