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SFDA: Announcement on Issues Related to Standardizing the Regulation of Products in the Class of Fibrinous Mucus
(Directive; Document No: GuoShiYaoJianBan[2006]523; Promulgation Date: 2006-09-30)
Letter of Replying Issues Related to Drug Excipients Using Local Approval Number
(Directive; Document No: ShiYaoJianZhuHan[2006]102; Promulgation Date: 2006-09-28)
SFDA’s Registration Department: Notification on Issues Related to “Radix Puerariae, Cortex Phellodendri and Lonicera japonica Thunb (Honeysuckle)” Listed in “Chinese Pharmacopoeia of 2005 (Section One)”
(Directive; Document No: ShiPinJianZhuHan [2006]69; Promulgation Date: 2006-07-06)
SFDA: Notification on Standardizing the Specification Description of BCG Polysaccharide and Nucleic Acid Preparation
(Directive; Document No: GuoShiYaoJianZhu[2006]253; Promulgation Date: 2006-06-13)
China Pharmacopoeia Committee: Letter of Correcting Related Contents in Drug Standard of “ShuGanXiaoJi(Relax Liver and Eliminate Indigestion) Pill”
(Directives; Document No: GuoYaoDianZhongFa[2006]100; Promulgation Date: 2006-04-10)
China Pharmacopoeia Committee: Letter of Correcting Related Contents in Drug Standard of “AnChuan(Relieve Pant) Tablet”
(Directives; Document No: GuoYaoDianFa[2006]88; Promulgation Date: 2006-03-24)
China Pharmacopoeia Committee: Letter of Correcting Related Contents in Drug Standard of “ZhenYin(Inhibit Psoriasis) Cream”
(Directives; Promulgation Date: 2006-03-30)
SFDA: Notification on Printing and Distributing “Technical Review Guideline for Combinations of β-Lactamase Inhibitor and Antibiotic(s)”
(Directive; Document No.: GuoShiYaoJianZhu[2006]44; Promulgation Date: 2006-02-06)
SFDA: Notification on Revising “Package Insert of Potassium Dehydroandrograpolide Succinate For Injection”
(Directive; Document No: GuoShiYaoJianZhu[2005]561; Promulgation Date: 2005-11-25)
SFDA: Notification on Printing and Distributing Guidelines for Writing Basic Content of Clinical Trail Report of Vaccines
(Directive; Document No.: GuoShiYaoJianZhuHan[2005]86; Promulgation Date: 2005-10-12)
SFDA’s Registration Department: Notification on Promulgating Guidelines for Submitting Registration Applications for Preventive Biological Products
(Directive; Document No.: ShiYaoJianZhuHan[2005]85; Promulgation Date: 2005-10-10)
General Administration of Quality Supervision, Inspection and Quarantine: Emergent Notification on Strengthening Supervision and Administration of Food Quality and Safety
(Directive; Document No: GuoZhiJianJian[2005] 182; Promulgation Date: 2005-06-02)
Department of Drug Registration of SFDA: Letter on Printing Requirements on Application Data for the Registration of Pharmaceutical
(Directive; Document No: GuoShiYaoJianZhuHan[2005]61; Promulgation Date: 2005-06-21)
SFDA: Notification on Related Affairs of Implementing “Administrative Provisions for Drug Registration”
(Directive; Document No: GuoShiYaoJianZhu[2005]328; Promulgation Date: 2005-06-20)
SFDA: Notification to Revise and Apply Registered Enterprise Standard of Preventative Biological Products
(Directive; Document No: GuoShiYaoJianZhu[2005]46; Promulgation Date: 2005-05-19)
SFDA: Notification on Regulating Registration and Purifying Registration Conditions
(Directive; Document No: GuoShiYaoJianZhuHan[2005]40; Promulgation Date: 2005-04-25)
SFDA: Notification on Certain Issues Concerning Drug GMP Certification
(Directive; Document No: GuoShiYaoJianAn[2004]108; Promulgation Date: 2004-04-12)
SFDA: Notification on Promulgating Provisions for the Qualification Authorization for Institutions Carrying out Drug Clinic Trial (Trial)
(Directive; Document No: GuoShiYaoJianAn[2004]44; Promulgation Date: 2004-02-19)
SFDA: Notification on Promulgating Drug Standard Improvement Action Plan
(Directive; Document No: GuoShiYaoJianZhu[2004]35; Promulgation Date: 2004-02-12)
SFDA: Announcement on Procedures for the Examination of the Documents Required to Imported Drug Re-registration
(Directive; Document No: GuoShiYaoJianZhu[2004]9; Promulgation Date: 2004-01-14)
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