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GUIDELINES
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GUIDLINES
Guidelines.
Title
Category
001 Guidelines for Allopathic Drugs CTD
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002 Guidelines for Registration of Allopathic Medicines
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003 Guidelines for Registration of Medical Devices
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004 Guidelines for Registration of Cosmetics and Household
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005 Guidelines for Registration of Food Supplements
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006 Guidelines for Registration of Herbal Medicines
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007 Guidelines for Homeopathic Drugs
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008 Guidelines for Registration of Vaccines and Other Biological Products
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009 Guidelines for Biological Products
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010 Guidelines for Bio-Similar Products
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011 Guidelines for Bio-Equivalence
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012 Guidelines for Stability
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013 Guidelines for Advertisement
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014 Guidelines for Fast Track Registration
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015 Guidelines for Variation of Allopathic Drugs
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016 Requirements for Labelling
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017 Guidelines for Listing of Specialized Products
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018 Guidelines for Clinical Trials Final2
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019 Guideline for ADR
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020 Safety of Medicines in ECOWAS Recent
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021 Material Transfer Agreement
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022 Current Guidelines for Application for ECOWAS PHC Licenses
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023 Guidelines for Conducting Research
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024 Guidelines for Change Business Ownership
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025 Guidelines for Internship Programme for ECOWAS PHC Technicians
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026 Guidelines for for Cultivation and Processing of Medical Cannabis
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027 Guidelines for Importation and Clearance of Controlled Drugs
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029 Guidelines for Receipt of Samples in the Lab
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030 Guidance on Good Manufacturing Practices Inspection Report
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031 Guidelines for Drugs Destruction
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032 Guidelines for Licensing of Manufacturing of Drugs and Cosmetics
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033 Guidelines GDP
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034 ECOWAS PHC Guidelines Small Scale Industries
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035 ECOWAS PHC Board Draft Guideline on Core SMPC and Package Leaflet for Fludeoxyglucose
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036 Draft Guidelines on Current Good Radio ECOWAS PHC
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037 Guidelines on Good Manufacturing Practices for Radio Pharmaceutical Products
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038 Procedure Guidelines for the Use of Radiopharmaceuticals
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039 Good Storage Practices
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Attachment 021 ECOWAS PHC MTA Template
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Attachment ECOWAS PHC . 001.01 Sample Schedule Pharmaceutical Products
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Attachment ECOWAS PHC . GL . 003.01 Sample Schedule Medical Device
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Inspection Guidelines
MS Word
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Listing of Specialised or Orphan Products for Importation
Microsoft Word
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Materials Transfer Agreement (MTA) Template
PDF
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ECOWAS PHC-F-78.1 Clinical Trial Application Form
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Requirements For Material Transfer Authorisation
PDF
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Food
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Herbals & Cosmetics
Vaccines, Biologicals & Medical Devices
Chemicals
Narcotics
Veterinary
Guidelines.