This supplier management webinar training will discuss the QSR and ISO requirements for supplier evaluation and assessment along with teach how to do supplier related corrective action.
Why You Should 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 compliance with the regulations. This presentation will briefly review the QSR and ISO requirements for supplier evaluation and assessment, and provide recommendations for cost efficient, streamlined, 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.
Who will benefit:
This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:
- Purchasing management
- Regulatory Management
- QA management
- Consultants
Instructor Profile:
Jeff Kasoff, RAC, is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is responsible for oversight of corporate compliance with domestic and international regulations, preparation of submissions, and is primary liaison with regulatory agencies and notified bodies. Jeff began his regulatory career as the first full-time employee of Optex Biomedical, a device start-up, where he initiated their regulatory policies and procedures and prepared their submissions. Jeff received his Regulatory Affairs Certification in 1996.
