FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes

Speaker

Instructor: Jeff Kasoff
Product ID: 701143

Location
  • Duration: 60 Min
This training will provide a solid understanding of FDA Requirements for Device Labeling. Attendees will gain comprehensive knowledge on creation, approval and control of labels and labeling.
RECORDED TRAINING
Last Recorded Date: Aug-2013

 

$229.00
1 Person Unlimited viewing for 6 month info Recorded Link and Ref. material will be available in My CO Section
(For multiple locations contact Customer Care)

$299.00
Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
(For multiple locations contact Customer Care)

 

 

Customer Care

Fax: +1-650-362-2367

Email: [email protected]

Read Frequently Asked Questions

Why You Should Attend:

Your  company's marketing department wants to entice customers to buy your product instead of your competitor's! A common method is to make the labeling as eye-catching as possible. Be careful! You need to know what information can (and more importantly) CANNOT be present on the labeling. Sometimes mislabeling and aggressive labeling can put you in to trouble.

This FDA labeling webinar will provide a comprehensive knowledge of labeling development and subsequent control. The updated FDA requirements and expectations regarding labeling contents will be covered. We will discuss the recommended best practices  and how to follow it to assure substantial compliance. This presentation provides comprehensive knowledge of labeling development and subsequent control. FDA requirements and expectations regarding labeling contents will be covered, as will recommended practices to assure compliance.

Areas Covered in the seminar:

  • Prescription Device Labeling.
  • Misbranding, False Or Misleading Labeling.
  • Approval.
  • Issuance.
  • Label Integrity.
  • Label Inspection.
  • Contractor-Produced Labels As A Linkage With Purchasing Controls.
  • Retention.
  • When a labeling change requires a new submission.

Who will benefit:

This webinar is designed for those who perform, supervise, manage, audit, or oversee the creation, approval, control of labels and labeling:

  • Regulatory Affairs management
  • Document Control (label generation) professionals
  • Design Control professionals
  • Quality Assurance professionals
  • Sales/marketing management

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.

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Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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