Showing 81–96 of 155 results
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Ministerial Ordinance 179: Good Manufacturing Practices for Drugs
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Ministerial Ordinance No. 36: Good Clinical Practice for Medical Devices
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Ministerial Ordinance No.2 Regulations for Facilities of Pharmacies in Japan
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Ministerial Ordinance No.21 – Good Laboratory Practice for Nonclinical Safety Studies of Drugs
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Ministerial Ordinance on Good Clinical Practice for Drugs
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Ministerial Ordinance on Good Laboratory Practice for Nonclinical Safety Studies of Medical Devices
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NMPA Guideline: Clinical Trial of Orthokeratology Rigid Gas Permeable (RGP) Contact Lenses in China
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NMPA Order No.82, 2020: the Issuance of Working Procedures for Review of Breakthrough Therapies in China
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NMPA Technical Guidelines: Application of Phase I Clinical Trials of New Drugs in China
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NMPA: Guidance for Clinical Evaluation of Proton/Carbon Ion Therapy System
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NMPA: Guidelines on Registration of Rare Disease Control Medical Devices
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NORMATIVE INSTRUCTION DESCRIBES THE CLASSIFICATION OF RISK OF CADASTRO AND REGISTRO REGISTRATIONS FOR IN VITRO DIAGNOSTIC PRODUCTS
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Notification 743/1998 : Guideline for Clinical Evaluation of Antibacterial Drugs
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Notification No. 0620-6 – Study Data for New Drug Applications
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Operation Specification for Record Filing of Medical Device Master Files
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Order No. 15 of the State Food and Drug Administration: Classification Rules for Medical Devices
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