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HUM-MOLGEN
-> Events
-> Meetings and Conferences |
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June 20, 2012 |
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ComplianceOnline, Online Event
2012-07-12
Why Should You Attend: Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in complliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices. Areas Covered in the Seminar:- QSR and ISO 13485 requirements for supplier selection and assessment.
- How to qualify new suppliers in a cost efficient manner.
- How to assess current suppliers in a cost efficient manner.
- How to perform supplier-related corrective action.
- Minimum documentation requirements for supplier qualification, assessment, and related corrective action.
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Organized by:
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ComplianceOnline |
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Invited Speakers:
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Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of consumables and instrumentation in the endoscopy field. In this position, Jeff is responsible for oversight of the quality system, including phase approval of design history files. For the past 13 years, Jeff served as Director of Regulatory Affairs at Life-Tech, Inc., where he was responsible for corporate compliance
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Deadline for Abstracts:
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2012-07-12
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Registration:
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For Registration:
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E-mail:
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referral@complianceonline.com
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WWW: Kai Garlipp,
Frank S.
Zollmann.
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