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Speaker Profile


Bernice Russell Bond
President, Brussell Consulting Inc

As President of BRUSSELL Consulting, Inc (BCI), Bernice brings over fifteen years of business operations, risk management, audit and compliance experience. She has worked for business, legal, audit, and IT management groups within various industries including manufacturing, financial and pharmaceutical. She has acquired practical insights, exposure to leading compliance practices, and seasoned judgment based on her work supporting the Compliance and IT Groups of Global Companies. In addition to her experience, Bernice also has the following academic credentials: B.S. in Accounting from Hampton University and an M.B.A with an emphasis in Technology Management from the University of Phoenix.

Upcoming Webinars
The HITECH Acts Impact on HIPPA
The new requirements of the HITECH Act have a significant impact on the privacy and security of health information.
Live  Thursday, October 14, 2010 10:00 AM PDT | 01:00 PM EDT,  Duration:60 Minutes
$165.00
...more

Recorded Webinars
Is your Laboratory Information Management System (LIMS) in compliance with 21 CFR Part 11 Subpart B - Electronic Records?
This webinar has been developed to provide clarification and interpretation on how to use LIMS in compliance with FDA Electronic Signatures and Electronic Records Rules.
Recorded ,
$295.00

Are you on the correct path to ensure compliance of your Information Systems with 21 CFR Part 11?
This Webinar would benefit company personnel that are responsible for the procedural and/or software requirements to ensure compliance with Part 11 of Title 21 of the Code of Federal Regulation.
Recorded ,
$295.00

Mitigate the risk that Excel Spreadsheets introduce to your company’s IT and operational environment under 21 CFR Part 11
End User Computing can be audited and control by manual process; using automated tools; or by the ideal method eliminating the need for end user computing by incorporating the computations to information systems controlled by the information technology department.
Recorded ,
$295.00

How Control Frameworks document compliance with Sarbanes Oxley (SOX), Section 404
Many have questioned whether the Sarbanes-Oxley law requirements can be met in a cost-efficient manner.
Recorded ,
$295.00

Risk Management Frameworks - Why are they important and Why have them
This webinar has been developed to provide clarification and interpretation on how to use LIMS in compliance with FDA Electronic Signatures and Electronic Records Rules.
Recorded ,
$295.00

What Controls need to be in place to reduce the risk of compromising Electronic Personally Identifiable Information (PII)
Prior to the development of a new system or the modification of an existing application that will collect, process and/or store PII, business reasons supporting these practices must documented.
Recorded ,
$295.00

Understanding good Closed Loop CAPA system
Increased regulatory pressures, the latest customer mandates and internal quality initiatives are requiring companies to take a proactive and automated approach to their corrective action process.
Recorded ,
$215.00

The HITECH Acts Impact on HIPPA
The new requirements of the HITECH Act have a significant impact on the privacy and security of health information.
Recorded ,
$215.00
...more