Guidance for Industry Submitting Marketing Applications According to the ICH-CTD Format — General Considerations DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. - International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use - Document - PDFSEARCH.IO

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Food and Drug Administration Pharmaceutical industry Clinical Data Management Drug safety Common Technical Document New Drug Application International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Center for Biologics Evaluation and Research Clinical research Research Medicine		Guidance for Industry Submitting Marketing Applications According to the ICH-CTD Format — General Considerations DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 49,70 KB Share Document on Facebook

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