Laboratory Record Keeping 2016 - Conference on Laboratory Record Keeping and Compliance
Date2016-10-20 - 2016-10-21
Deadline2016-10-18
VenueDouble Tree by Hilton Hotel San Francisco Airport,835 Airport Blvd, USA - United States
KeywordsLaboratory Record Keeping; Good Laboratory Practice; Standard Operating Procedures
Websitehttps://goo.gl/OLZH4K
Topics/Call fo Papers
Course "Fundamental Laboratory Record Keeping and Compliance Issue" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
Most of the focus on a laboratory’s 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. IF or 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. IF or 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
Agenda:
Day 1 Schedule:
Lecture 1: Recordkeeping and Archiving - Who, what, when, where, why, and how
Lecture 2: Who is responsible - what are the roles?
Lecture 3: What things must be recorded and archived?
Lecture 4: Why is this important?
Lecture 5: Where are specific things recorded and archived?
Lecture 6: How and how and how and how?
Day 2 Schedule:
Lecture 1: Basic laboratory operations
Lecture 2: Sample entrance and records
Lecture 3: Sample handling and storage
Lecture 4: Sample preparation
Lecture 5: Weighing, volumetric glassware, labeling
Lecture 6: Sample solution handling and records
Lecture 7: Stability testing!
Lecture 8: Instrument and maintenance logs
Lecture 9: Calibration logs
Lecture 10: Prevention through Control Chart Use
Lecture 11: Troubleshooting
Lecture 12: Safety
Speaker:
John Fetzer
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: SFO, CA Date: October 20th & 21st, 2016 and Time: 9:00 AM to 6:00 PM
Venue: Double Tree by Hilton Hotel San Francisco Airport, 835 Airport Blvd., Burlingame CA 94010-9949
Price:
Register now and save $200. (Early Bird)
Price: $1,295.00
Until September 15, Early Bird Price: $1,295.00 from September 16 to October 18, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Until September 15, Early Bird Price: $6,475.00 from September 16 to October 18, Regular Price: $7,475.00
Quick Contact:
NetZealous DBA as GlobalCompliancePanel
Phone: 1-800-447-9407
Fax: 302-288-6884
Email: support-AT-globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com
Registration Link - https://goo.gl/OLZH4K
Follow us: https://www.linkedin.com/company/globalcompliancep...
Overview:
Most of the focus on a laboratory’s 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. IF or 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. IF or 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
Agenda:
Day 1 Schedule:
Lecture 1: Recordkeeping and Archiving - Who, what, when, where, why, and how
Lecture 2: Who is responsible - what are the roles?
Lecture 3: What things must be recorded and archived?
Lecture 4: Why is this important?
Lecture 5: Where are specific things recorded and archived?
Lecture 6: How and how and how and how?
Day 2 Schedule:
Lecture 1: Basic laboratory operations
Lecture 2: Sample entrance and records
Lecture 3: Sample handling and storage
Lecture 4: Sample preparation
Lecture 5: Weighing, volumetric glassware, labeling
Lecture 6: Sample solution handling and records
Lecture 7: Stability testing!
Lecture 8: Instrument and maintenance logs
Lecture 9: Calibration logs
Lecture 10: Prevention through Control Chart Use
Lecture 11: Troubleshooting
Lecture 12: Safety
Speaker:
John Fetzer
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: SFO, CA Date: October 20th & 21st, 2016 and Time: 9:00 AM to 6:00 PM
Venue: Double Tree by Hilton Hotel San Francisco Airport, 835 Airport Blvd., Burlingame CA 94010-9949
Price:
Register now and save $200. (Early Bird)
Price: $1,295.00
Until September 15, Early Bird Price: $1,295.00 from September 16 to October 18, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Until September 15, Early Bird Price: $6,475.00 from September 16 to October 18, Regular Price: $7,475.00
Quick Contact:
NetZealous DBA as GlobalCompliancePanel
Phone: 1-800-447-9407
Fax: 302-288-6884
Email: support-AT-globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com
Registration Link - https://goo.gl/OLZH4K
Follow us: https://www.linkedin.com/company/globalcompliancep...
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Last modified: 2016-09-02 15:30:41