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HomeDrugsDrug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA Clic-Loc Child Resistant Closure Regulations

Filing a DMF for Clic-Loc Child Resistant Closure with the U.S. FDA

Filing a drug master file (DMF) for Clic-Loc Child Resistant Closure can be a useful mechanism to market your Clic-Loc Child Resistant Closure to the U.S. Drug Industry. Typical Clic-Loc Child Resistant Closure producers who have filed a DMF for Clic-Loc Child Resistant Closure include:

  - Owens Illinois Inc

Registrar Corp can help you to properly prepare and submit your Clic-Loc Child Resistant Closure DMF to FDA.

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

  - Format, assemble and deliver your Clic-Loc Child Resistant Closure DMF to FDA
  - Submit letters of authorization regarding your Clic-Loc Child Resistant Closure to FDA
 - Provide changes, additions and maintenance of your Clic-Loc Child Resistant Closure DMF
  - Respond to issues relating to ownership of your Clic-Loc Child Resistant Closure DMF
  - Assist with submission of responses to FDA concerning your Clic-Loc Child Resistant Closure DMF
  - Perform any required annual updates for your Clic-Loc Child Resistant Closure DMF

For more information about filing a DMF for Clic-Loc Child Resistant Closure, simply click below:




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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.
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