Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel

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Category Health Care, Medical Device, Compliance Training

Deadline: April 26, 2011 | Date: April 26, 2011

Venue/Country: Wilmington, U.S.A

Updated: 2011-03-31 19:08:40 (GMT+9)

Call For Papers - CFP

This session will allow your team to anticipate the auditors needs and result in the facility's ability to achieve the maximum benefit and score from the audit.

Why you should attend: More and more customers are requiring GFSI audits such as ISO 22000, BRC and SQF or accepting them in lieu of their own audits. Without passing scores on these audits, companies are losing current accounts and are denied access to new accounts and business. Many organizations are new to the process of audits and associated standards. Thus, they are seeking out expensive consultations and/or are requesting pre-assessments to prepare for audits. In order to work cost effectively, allocating resources and dollars to professional help with developing better systems rather than simply reviewing current programs, the supplier will be given the tools necessary to do its own preassessment and gap analysis. Audit results are as much a function of proper preparation as day to day operations. Find out what you need to know to achieve success.

Areas Covered in the Session:

* Description of the various audit schemes.

* Common methods of preparation

* Unique requirements

* Unspoken rules

* Tips for scheduling and executing a successful audit

* Guidelines for preparing corrective actions

Who will benefit:

* Auditors

* Senior Plant management and staff

Price List:

Live : $165.00

Corporate live : $695.00

Recorded : $215.00