GlobalCompliancePanel to organize RAPS pre-approved webinar on "Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements"
"Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner" is the topic of a 60-minute, RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on December 4. This webinar, which earns up to 1.00 RAC credits towards a participant's RAC recertification.
- Washington, DC-MD-VA-WV (1888PressRelease) December 04, 2012 - Both QSR regulations and ISO standards require supplier qualification and assessment. Since this is a necessary part of activity a medical device manufacturer has to carry out on a day-to-day basis; it makes business sense to evolve ways by which the manufacturer can cut down costs on this process.
Many device manufacturers spend a great deal of money on what is a routine activity. Does it really need to spend this much? It does not need to, but most companies end up spending because they are unaware of cost-effective methods.
This webinar will offer participants just this: A cost-effective method of carrying out supplier qualification and assessment and still meetFDA QSR and ISO 13485 requirements. It will equip participants with means to come up with less expensive ways of dealing with supplier qualification and assessment without compromising on FDA QSR and ISO 13485 requirements
When:December 4, 10:00 AM PDT | 01:00 PM EDT
By whom:
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. In this position, Jeff holds the critical portfolio of being responsible for oversight of corporate compliance with domestic and international regulations and preparation of submissions, and is the primary liaison point with regulatory agencies and notified bodies.
Performing such challenging tasks day in and day out has given Jeff deep knowledge of regulatory affairs, which he has imparted in the dozens of webinars he has presented in many areas dealing with regulatory compliance. 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. Delivering on challenges has thus never been new to Jeff. Jeff received his Regulatory Affairs Certification in 1996.
For whom:
o Purchasing Managers
o Regulatory Managers
o QA Managers
o Consultants
Duration: 60 minutes
To enroll for this webinar, contact
webinars ( @ ) globalcompliancepanel dot com
Phone: 800-447-9407
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