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.
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
Day One:
Lecture 1: Defining a Quality Management System (QMS)
Lecture 2: Management Components of a QMS
· Organization
· Quality System
· Document Control
· 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
· Internal Audits
· Management Review
Day Two:
Lecture 1: 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
Michael Brodsky
President, Brodsky Consultants
Michael Brodsky has been an Environmental Microbiologist for more than 41 years. He is a Past President of the Ontario Food Protection Association and AOAC International. He serves as Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC OMA and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and as a chapter editor on QA for the Compendium of Methods in Microbiology. He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is a member of the Board of Directors.
Location: Boston, MA Date: August 27th & 28th, 2015 Time: 9 AM to 6 PM
Venue: Courtyard Boston Logan Airport
Venue Address: 225 William F. McClellan Highway - Boston, Massachusetts 02128 USA
Price: $1,295.00 (Seminar for One Delegate)
Register now and save $200. (Early Bird)
Until July 15, Early Bird Price: $1,295.00
From July 16 to August 25, Regular Price: $1,495.00
Contact Information:
NetZealous LLC,
DBA GlobalCompliancePanel
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA
USA Phone: 800-447-9407
Fax: 302-288-6884
support@globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Registration Link - http://bit.ly/1by6MYj
Overview: The main document from a regulatory perspective in the development...
Q
Overview: This seminar is mainly based on the IEC62304:2006 standard and will...
Q
Overview: This course will present, in one place, the regulations and...
Q
Overview: We will be discussing the history and evolution of HIPAA...
Q
Overview: This two day seminar will provide the foundation for the...
Q
Overview: Most specialists strongly recommend to sample every meter of the...
Q
Overview: QMS is the catch phrase for accreditation and is the backbone of...
Q
Overview: This hands-on course will provide attendees with an understanding of...
Q
Overview: Upon completing this course participants should: · ...
Q
Overview: Prior to developing a process control plan as part of an overall...
Q
Overview: Topics included will include the filing of New Drug Submissions for...
Q
Overview: This course provides a basic overview of the laws and regulations...
Q
Overview: Why companies are prone to having past problems in new devices? One...
Q
Overview: The 2-day seminar begins with an examination of ISO and FDA...
Q
Overview: Prior to developing a process control plan as part of an overall...
Q
Overview: This program is designed to provide participants...
Q
Overview: FDA's and the Customs and Border Patrol Service (CBP) have become...
Q
Overview Throughout 21 CFR and guidance documents for the pharmaceutical,...
Q
Overview: We will be discussing the history and evolution of HIPAA...
Q
Overview: The FDA's Quality System Regulation (QSR) requires device...
Q
Overview: This 2-day seminar provides a 1-day introduction to the statistical...
Q
Overview: With all of the deadlines, projects, and tasks that you have to do...
Q
Overview: Real world examples of what to expect, and what to prepare for...
Q
Overview: This course provides a basic overview of the laws and regulations...
Q
Overview: Upon completing this course participants should: · ...
Q
Overview: The FDA recalls related to software performance are on the increase...
Q
Overview: Prepare yourself to take on the role of the Corporate Controller....
Q
Login to comment