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FDA Registration or FDA registration number does not denote FDA certification or FDA approval of your facility or products. Any representation of FDA registration number on product label or labeling which implies FDA certification or FDA approval of
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Request for meetings, courtesy calls and other related concerns – odg@fda.gov.ph. E-portal concerns (user account, change of usename, password and others) – fdac@fda.gov.ph. Filing of complaints – eReport@fda.gov.ph. Release of authorizations – records-releasing@fda.gov.ph. Payment concerns – cashier@fda.gov.ph.
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Many of our products are validated/verified by agencies such as US EPA, USDA, USGS, FDA, Japanese Ministry of the Environment, and WHO. Eurofins Abraxis holds, or is exclusive licensee, of several key technology patents, with additional applications in process.
The FDA ”Botanical Drug Development Guidance for Industry opens doors for botanical products like herbal medicines and cannabis-derived products to develop into prescription drugs; if a drug product is a single plant or from a mix of plants, the Guidance waives the requirement of 2) describing the mechanism of action.
ISO 13485 & ISO 9001 certified and FDA CGMP compliant. Conductive Technologies is pleased to announce a continuance of our EN ISO 13485, ISO 13485, and ISO 9001 Certification. #QualityMatters ( Read More )
White Oak Campus Information Site Address: 10903 New Hampshire Avenue, Silver Spring, MD 20993 Currently, the FDA White Oak Campus consists of ten office and four laboratory buildings, totaling 3.1 million rentable square feet.
All Sci-Pharm materials are manufactured and tested in accordance with applicable standards of the Food and Drug Administration (FDA) and International Organization for Standardization (ISO 13485:2016).