Medical Device Supplier Quality Agreements - Webinar By GlobalCompliancePanel

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Category online training,,Medical Device Supplier Quality Agreements,Quality System Regulation ,QSIT,13485 2003,FDA Quality System Inspection Technique ,Warning Letters

Deadline: June 20, 2012 | Date: June 20, 2012

Venue/Country: Online Training, U.S.A

Updated: 2012-05-09 18:16:26 (GMT+9)

Call For Papers - CFP

Why should you attend: Effective supplier management can help prevent problems and reduce their impact should they occur. With the increased emphasis on supplier management, you can expect strong coverage of this area during an FDA Inspection.

You need to understand the QSR requirements, good business practices, and the role of a quality agreement. This webinar will help you set up an effective system.

Areas Covered in the Session:

Valuable documents that provide understanding

Quality System Regulation (QSR), including the definitions

QSR Preamble

ISO 13485:2003

FDA's Quality System Inspection Technique (QSIT) manual

Warning Letters

Subject Areas covered

QSR Requirements for Purchasing

The Supplier Quality Agreement

Administrative Elements

Compliance

Manufacturing, Packaging, and Labeling

Documentation and Records

Storage and Shipment

Change Control

Non-Conformance, CAPA, and Complaints

Auditing

For each subject area, the webinar includes information from the valuable documents listed above

Who will benefit:

Quality Managers

Regulatory Affairs Managers

Risk Managers

Supply Chain Managers

Purchasing Professionals

Supplier Management Team

Customer Complaint Specialists

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00

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