MEDICAL DEVICES TRAINING ON QSR AND ISO REQUIREMEN 2015 - A Bulletproof, Cost-Efficient Supplier Management Program

Website http://bit.ly/1yUQY5Q | Edit Freely

Category Pharma

Deadline: January 28, 2015 | Date: January 28, 2015

Venue/Country: 2600 E. Bayshore Road, U.S.A

Updated: 2014-12-16 19:00:11 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Supplier qualification and assessment is required according to both QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this.

Organizations can, however, 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. It will also provide cost efficient and equally compliant options for many of the most common practices in supplier management programs.

Areas Covered in the Webinar:

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.

Who Will Benefit:

This webinar will provide valuable assistance to all regulated companies that are interested in implementing a supplier management program that is both compliant and cost-efficient. The employees who will benefit include:

Purchasing management

Regulatory management

QA management

Consultants

For registration:http://www.complianceonline.com/complying-with-fda-requirements-for-supplier-management-programs-webinar-training-700193-prdw?channel=Organic_Referral