Registrar Corp

HomeDrugsDrug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA AS30-J*PP AND AS50-J*PP Regulations

Filing a DMF for AS30-J*PP AND AS50-J*PP with the U.S. FDA

Filing a drug master file (DMF) for AS30-J*PP AND AS50-J*PP can be a useful mechanism to market your AS30-J*PP AND AS50-J*PP to the U.S. Drug Industry. Typical AS30-J*PP AND AS50-J*PP producers who have filed a DMF for AS30-J*PP AND AS50-J*PP include:

  - Yonwoo Corp

Registrar Corp can help you to properly prepare and submit your AS30-J*PP AND AS50-J*PP DMF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Format, assemble and deliver your AS30-J*PP AND AS50-J*PP DMF to FDA
  - Submit letters of authorization regarding your AS30-J*PP AND AS50-J*PP to FDA
 - Provide changes, additions and maintenance of your AS30-J*PP AND AS50-J*PP DMF
  - Respond to issues relating to ownership of your AS30-J*PP AND AS50-J*PP DMF
  - Assist with submission of responses to FDA concerning your AS30-J*PP AND AS50-J*PP DMF
  - Perform any required annual updates for your AS30-J*PP AND AS50-J*PP DMF

For more information about filing a DMF for AS30-J*PP AND AS50-J*PP, simply click below:




Live Help

 
U.S. FDA Regulations:

U.S. FDA DMF Regulation: 21 C.F.R. Section 314.420


Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2014 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco