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Pharmacokinetic/ Toxicokinetic Services

As your partner for drug development and regulatory strategy, Certara has expanded its services to offer GLP-compliant pre-clinical PK/TK NCA analysis and reporting.

Achieving Compliance with the FDA’s eCTD Mandate

The US Food and Drug Administration (FDA) has set 2018年5月5日 as the compliance date for submitting many types of files—Drug Master File (DMFs) and commercial investigational new drugs (INDs)—in the electronic Common Technical Document (eCTD) format. A DMF provides confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, … Continued

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