Developing Documents and Records to meet the Requirement of ISO 17025

Course "Developing Documents and Records to meet the Requirement of ISO 17025" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

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 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.

GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost

Why should you attend?

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 needs. 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?

Who will benefit:

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

Agenda:

Day 1 Schedule

Lecture 1: Organization Defining a Quality Management System (QMS)

Lecture 2: 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

Day 2 Schedule:

Lecture 3: Technical Components of a QMS

• Personnel
• 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
• Reporting the Results
• Technical Records

Speaker:

Michael Brodsky

President, Brodsky Consultants 

Michael has been an Environmental Microbiologist for more than 43 years. He is a Past President of the Ontario Food Protection Association (OFPA), The International Association for Food Protection (IAFP) and AOAC International. He serves as Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC Official Methods of Analysis and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and Wastewater, as a chapter editor on QA for the Compendium of Methods in Microbiology and as a member of ASTM Sub-committee D19.24 (Water Microbiology). He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is Vice-chair of the CALA Board of Directors.

Location: San Diego, CA Date: June 16th & 17th, 2016 and Time: 9:00 AM to 6:00 PM

Venue: WILL BE ANNOUNCED SOON

Price: $1,295.00 (Seminar fee for One Delegate)

 Register now and save $200.

Until April 20, Early Bird Price: $1,295.00 from April 21 to June 07, Regular Price: $1,495.00

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com      

Website: http://www.globalcompliancepanel.com

Registration Link - http://bit.ly/developing-documents-records-SFO   

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