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Toll Free: 510-857-5896 38868 Salmon Ter, Fremont California 94536 Live
Webinar
Auditing Laboratory Data Systems
http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500699LIVE?expDate=ACT_MARK_POWELL_JAN29_JAN22
Instructor: Mark Powell
http://www.onlinecompliancepanel.com/ecommerce/expertbio/~speaker_id=24825?expDate=ACT_MARK_POWELL_JAN29_JAN22
Date: Thursday, 29 January 2015
Time: 11:30 AM PST | 02:30 PM EST
Duration: 60 Minutes Price: $243.00 Live Session for one participant
Super combo offer Live + Training CD at $549.00
Webinar Description The effective auditing of laboratory data systems is
essential in order to ensure that the expectations of regulatory
agencies are met. This webinar will provide details of the most common
non-conformances and provide staff members, who are unfamiliar with
laboratory computer systems with an understanding of the controls that
are necessary to ensure the integrity of analytical data.
Register Now
http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500699LIVE?expDate=ACT_MARK_POWELL_JAN29_JAN22
Instructor Profile:
Mark Powell
Director, Mark Powell Scientific Limited,
http://www.onlinecompliancepanel.com/ecommerce/expertbio/~speaker_id=24825?expDate=ACT_MARK_POWELL_JAN29_JAN22
Dr Mark Powell is a Fellow of the Royal Society of Chemistry (RSC) with
over 20 years' experience as a senior analytical chemist. He is a member
of the RSC's Analytical Division Council and chairs their working group
on Continuing Professional Development. Until September 2013, he was
Scientific Manager for a pharmaceutical CRO specializing in early-stage
drug development. More...
http://www.onlinecompliancepanel.com/ecommerce/expertbio/~speaker_id=24825?expDate=ACT_MARK_POWELL_JAN29_JAN22
Why Should you Attend: The webinar will teach participants the
importance of correct data system configuration and what to look for
during the audit. Businesses will benefit by reducing the risk of
regulatory action as a result of failure to comply with current
expectations.
Objectives of the Presentation: The objectives of the presentation are
to cover areas such as:
Categories of laboratory data system (GAMP)
Lifecycle management, archiving and backup
What counts as raw data?
Protecting the integrity of analytical data
General guidance on assigning user privileges
Operating system configuration.
Application configuration
Controls appropriate for chromatography data systems
Practices that aid compliance with data integrity requirements
Examples from recent FDA warning letters
Who can Benefit:
Staff who are required to audit analytical operations who do not have a
chemical QC background.
Auditors who require updating on current regulatory expectations.
QC staff who needs help in regulatory compliance.
Staff who would like to understand the implications of data integrity
for laboratory data systems.
Register Now
http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500699LIVE?expDate=ACT_MARK_POWELL_JAN29_JAN22
About Us
http://www.onlinecompliancepanel.com/ecommerce/aboutus?expDate=ACT_MARK_POWELL_JAN29_JAN22
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