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Understanding and implementing an effective laboratory Quality Management System to comply with ISO/IEC 17025 (Part 1)

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Website https://www.demystifiedsolutions.com/trainingDetails/Understanding-and-implementing-an-effective-lab | Edit Freely

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Deadline: April 27, 2017 | Date: April 27, 2017

Venue/Country: Online

Updated: 2017-03-09 22:31:44 (GMT+9)

Call For Papers - CFP

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. The Quality System Manual (QSM) is the bible in a Quality Management System (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 the management requirements of the standard.

Why Should You Attend

Accreditation to international standards is being 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 17025:2005 but also meets their own needs and those of their customers.

Areas Covered in this Webinar

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

Learning Objectives

Policies vs. Procedures

Documents vs. Records

The importance of the KISS principle

The devil’s in the details

Who Will Benefit

- Laboratory Management/Supervision

- Laboratory Quality Development

- Laboratory Quality Management

- Laboratory Quality Control

- Analytical support

For More Info, Please Click below URL:

https://www.demystifiedsolutions.com/trainingDetails/Understanding-and-implementing-an-effective-laboratory-Quality-Management-System-to-comply-with-ISO-IEC-17025-Part-1-DEMY051436


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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