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bureau drug

bureau drug, Total:15 items.

In the international standard classification, bureau drug involves: Pharmaceutics.

EU/EC - European Union/Commission Legislative Documents, bureau drug

• COM(2016) 498 FINAL-2016 REPORT FROM THE COMMISSION Pharmacovigilance related activities of Member States and the European Medicines Agency concerning medicinal products for human use (2012 – 2014) (SWD(2016) 284 final)

US-FCR, bureau drug

• FCR 21 CFR PART 344-2013 TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
• FCR 21 CFR PART 344-2014 TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
• FCR 21 CFR PART 16-2015 REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
• FCR 21 CFR PART 16-2014 REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
• FCR 21 CFR PART 16-2013 REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION

Professional Standard - Agriculture, bureau drug

• 食药监办食监三函〔2014〕235号 Reply Letter from the General Office of the China Food and Drug Administration on the Qualification of the Illegal Addition of Drugs Phenolphthalein and Fluoxetine

US-HHS, bureau drug

• HHS 21 CFR PART 16 CFR PART 54-2011 REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION

British Standards Institution (BSI), bureau drug

• BS ISO 21371:2018 Traditional Chinese medicine. Labelling requirements of products intended for oral or topical use

US-CFR-file, bureau drug

• CFR 21-5.1110-2014 Food and drugs. Part5:Organization. SubpartM:Organization. Section5.1110:FDA public information offices.
• CFR 21-16.1-2014 Food and drugs. Part16:Regulatory hearing before the food and drug administration. SubpartA:General provisions. Section16.1:Scope.
• CFR 21-20.30-2014 Food and drugs. Part20:Public information. SubpartB:General policy. Section20.30:Food and Drug Administration freedom of information staff.
• CFR 21-20.107-2014 Food and drugs. Part20:Public information. SubpartF:Availability of specific categories of records. Section20.107:Food and Drug Administration manuals.
• CFR 21-10.90-2014 Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.90:Food and Drug Administration regulations, recommendations, and agreements.

IX-EU/EC, bureau drug

• COM(2013) 472 FINAL-2013 Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on fees payable to the European Medicines Agency for the conduct of pharmacovigilance activities in respect of medicinal products for human use (2013/0222 (COD); Text with EEA relevan

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