This course is available for non weights and measures participants. The concepts covered in the class are especially useful for other program applications, but the focus and activities are on laboratory procedures and applications. This webinar is also useful for administrative or management staff who help define the lab procedures or ensure items are filed/located appropriately for the laboratory. Laboratory personnel who have responsibilities for developing, implementing, and/or improving the quality management system in their laboratory as well as those who are seeking OWM recognition and/or accreditation or improvements to support recognition/accreditation. Successful completion includes completing pre-work assignment, full attendance, and participation in the session activities and discussions. Submit the pre-work to the instructor by COB on Thursday, August 3, 2023. Submit any related procedures that are in place in your laboratory related to 'Document Control'.

Record and submit the amount of time (in minutes) it takes you to complete the pre-work assignment to instructor when you email the assignment.

Write a short paragraph describing one challenge or difficulty you (or your laboratory) faces with document and record control.

8.3 (Control of Management System Documents), and.

7.11 (Control of Data and Information),.

Read ISO/IEC 17025:2017 (student is responsible for obtaining an official copy of this standard):.

There are no prerequisites for this webinar.

IDENTIFY the types of typical laboratory records that must be maintained.

EXPLAIN the relationship between documents and records and.

RECOGNIZE methods that are used to document revisions.

IDENTIFY the 5 phases of the document control process.

IDENTIFY at least 5 types of laboratory documents that must be controlled.

LIST 3 properties of management system documents that must be controlled.

Learning ObjectivesĪt the end of this session, using your notes and ISO/IEC 17025:2017 or NIST Handbook 143, you will be able to: This 2-hour webinar will introduce the fundamentals of Laboratory Management System Document Control and Record Keeping that are necessary to successfully implement ISO/IEC 17025:2017.

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