Understanding and Implementing an Effective Laboratory Quality Practice System : ISO 1725

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Category ISO 17025 Training; Good Laboratory Practice Training

Deadline: April 02, 2018 | Date: April 02, 2018

Venue/Country: Training Doyens 26468 E Walker Dr,Aurora, Colora, U.S.A

Updated: 2018-02-16 20:02:31 (GMT+9)

Call For Papers - CFP

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

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