Webinar Information


Understanding and Implementing an Effective Laboratory Quality Management System


Understanding and Implementing an Effective Laboratory Quality Management System, Denver, Colorado, United States
Webinar Title
Understanding and Implementing an Effective Laboratory Quality Management System
Event Type
Webinar
Webinar Date
02-04-2018
Last Date for Applying
02-04-2018
Location
Denver, Colorado, United States

Organization Name / Organize By
Training Doyens
Organizing/Related Departments
Training Doyens
Organization Type
Organization/Company
Webinar Category
Both (Technical & Non Technical)
Webinar Level
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Medical/Healthcare/Hospital

Location
Denver, Colorado, United States

OVERVIEW

Part 1

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025: The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. What is also needed are the “how to do it” or procedures and methods and finally the controls or evidence that it was done properly. This is the 1st of two webinars on this topic and focuses on complying with themanagement requirements of the standard.

Part 2

Many laboratories regard Quality Assurance, Quality Assessment and Quality Control as independent activities, others use the terms interchangeably, e.g. QA/QC. This demonstrates a lack of appreciation of the differences between Assurance, Assessment and Control, as well as the interrelationships, particularly between QA and QC. This has created confusion in the minds of many analysts with respect to understanding how QA and QC play separate, but related roles for achieving Quality Assurance in a Quality Management System (QMS).

WHY SHOULD YOU ATTEND

Part 1

Accreditation to international standards is becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require food and environmental laboratories to be accredited to ISO/IEC 17025 in order to participate in regulatory programs. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits. Why do you want to become accredited? Where do you start? For laboratories that are already accredited, how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? Many laboratories struggle with developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025b but also meets their own needs and those of their customers.

Part 2

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:Accreditation to international standards is becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require food and environmental laboratories to be accredited to ISO/IEC 17025 in order to participate in regulatory programs. This webinar is the 2nd in the series and will address how to develop and maintain the technical components of the QMS.

AREAS COVERED

Part 1

  • Management Components of a QMS
  • Document Control
  • Quality System
  • Review of Requests, Tenders and Contracts
  • Subcontracting of Tests and Calibrations
  • Purchasing Services and Supplies
  • Service to Customer
  • Control of Non-conforming Testing and/or Calibration Work
  • Control of Records
  • Internal Audits
  • Management Review
  • Personnel

Part 2

  • Accommodation and Environmental Conditions
  • Test and Calibration Methods and Method Validation
  • Equipment
  • Measurement Traceability
  • Sampling
  • Handling of Test and Calibration Items
  • Assuring the Quality of Test and Calibration Results

LEARNING OBJECTIVES

Part 1

  • Policies vs. Procedures
  • Documents vs. Records
  • The importance of the KISS principle
  • The devil’s in the details

Part 2

  • Technical Requirements of a QMS
  • Method Selection
  • Validation and Verification
  • Ensuring analytical competency

WHO WILL BENEFIT

  • Laboratory Management/Supervision
  • Laboratory Quality Development
  • Laboratory Quality Management
  • Laboratory Quality Control
  • Analytical support

 

For more detail please click on this below link:

http://bit.ly/2oOGbhw

 

Email: support@trainingdoyens.com

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616

Fax: +1-888-909-1882

Others Details

Webinar covering important aspects of laboratory accreditation andimplementing an effective laboratory quality management system.

Registration Fees
Available
Registration Fees Details
Live Session for one participant $199 Corporate Live Session Group – Max 10 Participants from one location. $549 Recorded Session Get unlimited access to audio recording of the webinar for 6 months. $219 Training DVD or USB Flash Drive MP3 files, PDF presentation and reference manual will be delivered on a CD $399 Super Combo Offer 1 Live and Recorded webinar $329 Super Combo Offer 2 Live and Training CD $479
Registration Ways
Email
Phone
Website
Other
Address/Venue
26468 E Walker Dr, Aurora, Colorado 80016  Pin/Zip Code : 80016
Landmark
CO
Official Email ID
support@trainingdoyens.com
Contact
Training Doyens

26468 E Walker Dr, Aurora, Colorado 80016-6104

support@trainingdoyens.com

   7209961616
Michael smith

26468 E Walker Dr, Aurora, Colorado 80016-6104

support@trainingdoyens.com

   7209961616    Fax No: Colorado City