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A Bulletproof, Cost-efficient Supplier Management Program

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A Bulletproof, Cost-efficient Supplier Management Program
Description

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 compliance 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.

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Live Webinar on : A Bulletproof, Cost-efficient Supplier Management Program

Tuesday, February 14, 2012 (60 Minute)







Description





Supplier qualification and assessment is

Get 15 % Discount as a early bird

required in both the QSR regulations and

registrations. Use Promo Key :

CGO15

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

compliance 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.

Who will benefit



Purchasing management



Regulatory management



QA management



Consultants





Areas Covered in the Session:







Pricing

- QSR and ISO 13485 requirements for

One Dial In - One Attendee: $189.00 supplier selection and assessment

One Dial In - Unlimited attendance (To

be arranged in a Conference

room/Meeting room. Note : Only One

Dial In Allowed): $249.00 - 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 corective action









About Speaker:



Jeff Kasoff, RAC, is the Director of Quality at

Byrne Medical, a leading manufacturer of

endoscopy products. In this position, Jeff is

responsible for supplier management, during which

he oversees supplier management, CAPA, and

document control. Prior to this, Jeff spent 13 years

at Life-Tech as the Director of Regulatory Affairs,

where he was responsible for regulatory

compliance of all aspects of the quality system. Jeff

received his regulatory affairs certification in 1996.









For any assistance contact us at support@compliance2go.com or call us at 877.782.4696





https://compliance2go.com/index.php?option=com_training&speakerkey=15&productKey=82


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