Laboratory Record Keeping and Compliance Issue Seminar in Boston
- September 26, 2016
- 524 Views
- 0 Likes
- 0 Comment
Most of the focus on a laboratorys compliance to Good Laboratory Practice (GLP) or to the analogous ISO 17025 is on items such as the Standard Operating Procedures, training, quality assurance testing, and the statistical assessment of performance and compliance/ These, however, are not all that an auditor may delve into. These might the bulk of an audit, yet a laboratory may fail an audit. Since laboratories focus on them, they might ignore more mundane and simple areas, such as recordkeeping and archiving, basic laboratory operations, and safety.
Why should you attend?
An auditor can find numerous common errors and many, many others that are specific. This seminar will go through many of the compliance areas and point out some of both types. IFor those implementing GLP or striving to maintain certification, this course should point out many areas to cover that would lessen an unsatisfactory audit.An auditor can find numerous common errors and many, many others that are specific. This seminar will go through many of the compliance areas and point out some of both types. IFor those implementing GLP or striving to maintain certification, this course should point out many areas to cover that would lessen an unsatisfactory audit.
Who will benefit:
Chemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025Chemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025
Day 1 Schedule
Recordkeeping and Archiving - Who, what, when, where, why, and how
Who is responsible - what are the roles?
What things must be recorded and archived?
Why is this important?
Where are specific things recorded and archived?
How and how and how and how?
Day 2 Schedule
Basic laboratory operations
Sample entrance and records
Sample handling and storage
Weighing, volumetric glassware, labeling
Sample solution handling and records
Instrument and maintenance logs
Prevention through Control Chart Use
Founder and Principal, Consultant Fetzpahs Consulting (510) 724-8629
John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers onl iquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
Location: Boston, MA Date: September 8th & 9th, 2016 and Time: 09:00 AM to 06:00 PM
Venue: WILL BE ANNOUNCED SOON
Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until August 5, Early Bird Price: $1,295.00 from August 26 to September 6, Regular Price: $1,495.00
Register for 5 attendees
Price: $3,885.00 ,
$6,475.00 You Save: $2,590.00 (40%)
Until August 5, Early Bird Price: $6,475.00 from August 6 to September 6, Regular Price: $7,475.00
NetZealous DBA as GlobalCompliancePanel
Registration Link - http://bit.ly/29uyt31-Laboratory-Record-Keeping
Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel