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Event :Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines

Dates :Thursday June 22nd, 2017 - Friday June 23rd, 2017

Location :Venue to be announced shortly
Philadelphia, United States

Type :Conference & Seminar - International audience

Accreditation :--


 

Further information

Course Description:

This course is designed to introduce to individuals the understanding and interpretation of the statistical concepts with reference to certain quantitative ICH Guidelines that apply across laboratory (drug development) and clinical development (drug/device) procedures such as analytical methods in validation and acceptance criteria in calibration procedures, risk management and process monitoring as well as dealing with uncertainties and other relevant issues. It is not a course in statistics but introduces the participant to a hands on approach to the statistical techniques one uses, how they are applied and reasonably interpreted and understood. One will address the various challenges facing pharmaceutical and biotechnology companies when it comes to quantifying results in a meaningful interpretable manner through tabulations and graphical presentations.

In this two day workshop seminar one will learn the different regulatory agencies expectations of the quantification and development of a sound statistical monitoring of process control that are accepted, effective, and efficient. Participants will become familiar with the important aspects of the statistical methods and learn how organizations are expected to apply these guidelines.

 

Learning Objective:

Upon completing this course participants should be able to:

  • Evaluate linear and other quantitative measurement procedures.
  • Distinguish the difference between confidence and tolerance intervals.
  • Evaluate the sensitivity of the sample size in given procedures.
  • Evaluate laboratory/clinical data results based on risk management and design space issues.
  • Interpret alternative approaches to statistical process control in reference to data distributional formats.
  • Discuss relevant FDA requirements and ICH guidelines.

 

Who will Benefit:

This course is designed for people responsible for developing, maintaining and/or improving clinical and laboratory monitoring programs and interpreting the results from such. This includes individuals that have data monitoring responsibilities. The following personnel will benefit from the course:

  • Quality Managers
  • Quality Professionals
  • Assay Development Scientists
  • Research Scientists
  • Clinical/Laboratory Data Analysts
  • Laboratory Data Managers

 

For Registration -  http://www.complianceonline.com/understanding-the-statistical-considerations-for-quantitative-ich-guidelines-seminar-training-80281SEM-prdsm?channel=doctorama         

 

Note: Use coupon code NB5SQH8N and get 10% off on registration.

Location

Map and directions
Conference address :
Venue to be announced shortly
Philadelphia
United States
Map and directions

Further information

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Details

Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines Pharmacy
statistical considerations for quantitative ich guidelines training, quantitative measurement procedures, sensitivity of the sample size
Everyone, Quality Managers Quality Professionals Assay Development Scientists Research Scientists Clinical/Laboratory Data Analysts Laboratory Data Managers
100 1 --
English

Other

For more information on Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines, plsase contactr ComplianceOnline

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