application type
- Guideline or reference source
- DIAEDM Guide to the DIA EDM reference model, process zone regulatory submissions
- Definition
- Type of application submitted to a Regulatory Authority as required to conduct clinical trials or gain authorization to market a regulated pharmaceutical product. Values dictated by Regulatory authorities.
- Broader Term
- application
- Narrower Term
- article 58 application
- hybrid application
- renewal
- Related Term
- abbreviated new drug application
- biologics license application
- clinical trial application
- drug master file
- investigational new drug application
- marketing authorization application
- new drug application
- submission type
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