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MPEP Q & A 336: Circumstances when relevant documentation should be submitted to regulatory review body.

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Manage episode 505531777 series 1537034
Content provided by Lisa Parmley, USPTO Patent Practitioner #51006, Lisa Parmley, and USPTO Patent Practitioner #51006. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Lisa Parmley, USPTO Patent Practitioner #51006, Lisa Parmley, and USPTO Patent Practitioner #51006 or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

Question: When should relevant documentation submitted to a regulatory review body be submitted for the Office for review? Answer: Where relevant documentation is submitted to a regulatory review body, such as the U.S. Food & Drug Administration (FDA), and is material to any pending patent application or reexamination proceeding, such documentation should be submitted for […]

The post MPEP Q & A 336: Circumstances when relevant documentation should be submitted to regulatory review body. appeared first on Patent Education Series.

  continue reading

310 episodes

Artwork
iconShare
 
Manage episode 505531777 series 1537034
Content provided by Lisa Parmley, USPTO Patent Practitioner #51006, Lisa Parmley, and USPTO Patent Practitioner #51006. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Lisa Parmley, USPTO Patent Practitioner #51006, Lisa Parmley, and USPTO Patent Practitioner #51006 or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.

Question: When should relevant documentation submitted to a regulatory review body be submitted for the Office for review? Answer: Where relevant documentation is submitted to a regulatory review body, such as the U.S. Food & Drug Administration (FDA), and is material to any pending patent application or reexamination proceeding, such documentation should be submitted for […]

The post MPEP Q & A 336: Circumstances when relevant documentation should be submitted to regulatory review body. appeared first on Patent Education Series.

  continue reading

310 episodes

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