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Filing a DMF for Exacta-Med(R) Oral Liquid Dispenser with the U.S. FDA

Filing a drug master file (DMF) for Exacta-Med(R) Oral Liquid Dispenser can be a useful mechanism to market your Exacta-Med(R) Oral Liquid Dispenser to the U.S. Drug Industry. Typical Exacta-Med(R) Oral Liquid Dispenser producers who have filed a DMF for Exacta-Med(R) Oral Liquid Dispenser include:


Registrar Corp can help you to properly prepare and submit your Exacta-Med(R) Oral Liquid Dispenser DMF to FDA.

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

  - Format, assemble and deliver your Exacta-Med(R) Oral Liquid Dispenser DMF to FDA
  - Submit letters of authorization regarding your Exacta-Med(R) Oral Liquid Dispenser to FDA
 - Provide changes, additions and maintenance of your Exacta-Med(R) Oral Liquid Dispenser DMF
  - Respond to issues relating to ownership of your Exacta-Med(R) Oral Liquid Dispenser DMF
  - Assist with submission of responses to FDA concerning your Exacta-Med(R) Oral Liquid Dispenser DMF
  - Perform any required annual updates for your Exacta-Med(R) Oral Liquid Dispenser DMF

For more information about filing a DMF for Exacta-Med(R) Oral Liquid Dispenser, 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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