Regulatory Support

SCHOTT filed different types of Drug Master Files (DMF) for Primary Packaging Material with the US Food and Drug Administration (FDA)Health Canada authorities and National Medical Products Administration (NMPA) in China containing information about Chemistry, Manufacturing and Control (CMC) of our pharmaceutical packaging products.

To allow the appropriate authorities to review our Drug Master Files in support of customer drug applications SCHOTT will provide free of charge a Letter of Authorization (LOA).

 

To request a LOA, please click the button:

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For further information you can contact us by using the following form:

Please note, that this form is not for transmitting LOA requests.
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SCHOTT AG promises that all data entered into a web form will only be used for internal purposes. For more detailed information, please refer to our data protection guidelines.

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