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PTO/SB/16 (0404) Approved for use through 07/31/2006. OMB 06510032 U.S. Patent and Trademark Office; U.S. DEPARTMENT OF COMMERCE Under the Paperwork Reduction Act of 1995, no persons are required
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Step 1: Go to the official Celltrion website.
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Step 2: Locate the 'Files Petition' section or page.
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Step 3: Read and understand the instructions and requirements for filling out the petition.
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Step 4: Gather all the necessary documents and information needed for the petition.
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Step 5: Fill out the specified fields in the petition form accurately and completely.
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Step 10: Follow any further instructions or actions required by Celltrion to complete the petition process.

Who needs celltrion files petition for?

01
Patients who have used or are currently using Celltrion products and have experienced any adverse effects or complications.
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Individuals who believe they have valid claims or concerns related to Celltrion's products, services, or actions.
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Medical professionals or researchers who have relevant information or evidence related to Celltrion's products or practices.
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Consumer advocacy groups or organizations working to protect the rights and interests of consumers in the healthcare sector.
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Legal entities involved in investigations or litigations related to Celltrion products or activities.
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Celltrion files petition for approval of new drugs or biologics.
Celltrion or any pharmaceutical company developing new drugs or biologics.
The petition must be filled out with detailed information on the new drug or biologic, including safety and efficacy data.
The purpose is to seek approval from regulatory authorities to market and sell the new drug or biologic.
Information such as clinical trial results, manufacturing process, and proposed labeling must be reported.
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