Suchen Sie nach Informationen zu FDA-Zentrale Weißeiche? Folgen Sie den Links unten, um alle Informationen zu finden, die Sie benötigen, und mehr.
https://www.fda.gov/about-fda/office-global-operations/europe-office
Established in May 2009, the Europe Office serves as the lead for the FDA’s Office of Global Policy and Strategy’s on-site presence in …
https://www.fda.gov/about-fda/contact-fda
Call 1-888-INFO-FDA (1-888-463-6332). Call the FDA Consumer Complaint Coordinator for your state or region. For more details, see How to Report a Problem.
The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by …
https://www.fda.gov/Drugs/
Medication Guides, Drug Safety Communications, Shortages, Recalls. Drug Approvals and Databases . Drugs@FDA, Orange Book, National Drug Code, Recent drug approvals. Drug Development and Review Process
https://www.fda.gov/industry/import-program-food-and-drug-administration-fda/import-offices-and-ports-entry
Use the map below to locate the applicable port of entry for your shipment and contact the corresponding Import Division. Learn more about the Nationalized Drug Entry Review Pilot. If you have ...
https://www.fda.gov/about-fda/fda-organization
FDA Organization. FDA is an agency within the Department of Health and Human Services. Effective March 31, 2019, FDA began operational implementation of an agency reorganization. FDA’s ...
https://www.fda.gov/Medical-Devices
Food and Drug Administration 10903 New Hampshire Ave Silver Spring, MD 20993. [email protected] (800) 638-2041 (301) 796-7100. Hours Available. Office of …
https://www.fda.gov/international-programs/confidentiality-commitments/fda-zentralstelle-der-lander-fur-gesundheitsschutz-bei-arzneimitteln-und-medizinprodukten-zlg-and
FDA is authorized under 21 C.F.R. § 20.89 2 to disclose non-public information to ZLG and the Länder regarding FDA-regulated drugs, including pre- …
https://www.usfda.info/fei/
FDA Compliance FDA Registration March 9, 2022. FDA recommends that at the time of registration, the owner or operator obtain an FEI Number. Firm Establishment Identifier (FEI) should be used for identification of entities within the imports message set. An FDA Establishment Identification (FEI) number is a unique identifier issued by the FDA to ...
https://www.statnews.com/2022/07/19/fda-weighs-oversight-changes-after-juul-formula-troubles/
The head of the FDA said he has commissioned an independent review of the agency's food and tobacco programs following months of criticism over its handling of the baby formula shortage and e ...
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