OPERATIONAL GUIDELINES
PHARMACEUTICAL AND ALLIED PRODUCTS GUIDELINES
TOBACCO SUBSTANCE ABUSE
- GUIDELINES FOR IMPORTATION OF CONTROLLED SUBSTANCES
- GUIDELINES FOR THE LABELLING OF TOBACCO PRODUCTS
- GUIDELINES FOR THE REGISTRATION OF TOBACCO PRODUCTS
- A GUIDE FOR MANAGERS ON THE PROHIBITION OF SMOKING IN PUBLIC PLACES
- RETURNS ON NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCES IMPORTED
- SPECIFICATIONS FOR NO-SMOKING SIGN
- SPECIFICATIONS FOR DESIGNATED SMOKING AREAS
HERBAL
BIOLOGICAL PRODUCTS
- (BR) BATCH RELEASE HEPATITIS A VIROSOMAL
- (BR) BATCH RELEASE OF BCG VACCINE
- (BR) BATCH RELEASE HEPATITIS A (INACTIVATED AND ABSORBED)
- (BR) BATCH RELEASE INFLUENZA
- (BR) BATCH RELEASE] MEASLES VACCINE
- (BR) BATCH RELEASE] POLIO
- (BR) BATCH RELEASE] HEPATITIS B
- (BR) BATCH RELEASE] WHOLE CELL DTP
- (BR) BATCH RELEASE] RABIES
- GUIDELINES FOR REGISTRATION OF BIOLOGICAL PRODUCTS
- GUIDELINES FOR REGISTRATION OF BIOSIMILAR PRODUCTS
- GUIDELINES FOR REGISTRATION OF WORLD HEALTH ORGANISATION (WHO) PRE-QUALIFIED BIOLOGICAL PRODUCTS
- GUIDELINES FOR APPLICATION TO IMPORT UNREGISTERED BIOLOGICAL PRODUCT FOR A NAMED PATIENT
- GUIDELINES FOR REPORTING VARIATIONS TO BIOLOGICAL PRODUCTS
- GUIDELINES FOR THE IMPORT AND EXPORT OF PATHOLOGICAL MATERIALS TO AND FROM GHANA
- GUIDELINES FOR REGISTRATION OF VACCINES
- GUIDANCE DOCUMENT FOR BLOOD FACILITY LICENSURE APPLICATION FORM
- GUIDELINES FOR LICENSING BLOOD FACILITIES AND BLOOD PRODUCTS LISTING
- GUIDELINES FOR EMERGENCY USE AUTHORIZATION OF MEDICAL PRODUCTS
- GUIDELINES FOR REGISTRATION OF PLASMA DERIVED MEDICINAL PRODUCTS
- GUIDELINES FOR REGISTRATION OF VETERINARY BIOLOGICAL PRODUCTS
SAFETY MONITORING
- GUIDELINES FOR ADVERSE REACTION REPORTING
- GUIDELINES FOR CONDUCTING PHARMACOVIGILANCE INSPECTIONS
- GUIDELINES FOR QUALIFIED PERSON FOR PHARMACOVIGILANCE
- SURVEILLANCE OF ADVERSE EVENTS FOLLOWING IMMUNIZATION IN GHANA
- GUIDELINES FOR SAFETY MONITORING OF MEDICINAL PRODUCTS
CLINICAL TRIALS
- GUIDELINES FOR GOOD CLINICAL PRACTICE IN GHANA
- GUIDELINES FOR AUTHORIZATION OF CLINICAL TRIALS OF MEDICINES, FOOD SUPPLEMENTS, VACCINES AND MEDICAL DEVICES IN GHANA
- GUIDELINES FOR CONDUCT OF CLINICAL TRIALS IN PAEDIATRIC POPULATION
- GUIDELINES FOR CONDUCT OF CLINICAL TRIALS DURING EMERGENCIES
DRUG ENFORCEMENT
- GUIDELINES FOR CGMP INSPECTION OF HERBAL MANUFACTURING FACILITIES LOCATED IN GHANA
- GUIDELINES FOR cGMP INSPECTION OF PHARMACEUTICAL MANUFACTURING FACILITIES
- GUIDELINES FOR ADVERTISEMENT OF DRUGS, MEDICAL DEVICES, COSMETICS AND HOUSEHOLD CHEMICALS
- GUIDELINES FOR LICENSING OF PHARMACEUTICAL AND HERBAL MEDICINES MANUFACTURING FACILITIES
- GUIDELINES FOR LICENSING STORAGE FACILITIES OF WHOLESALERS AND DISTRIBUTORS OF PHARMACEUTICAL PRODUCTS, HERBAL MEDICINES AND FOOD SUPPLEMENTS
- GUIDELINES FOR SAFE DISPOSAL OF UNWHOLESOME PRODUCTS
- SELECTION OF AUTHORIZED PERSON IN THE PHARMACEUTICAL AND CHEMICAL INDUSTRY
- GUIDELINES FOR PRODUCT RECALL
IMPORT & EXPORT CONTROL
- GUIDELINES FOR CLEARANCE OF IMPORTED PHARMACEUTICAL PRODUCTS
- GUIDELINES FOR CLEARANCE OF PHARMACEUTICAL PRODUCTS FOR EXPORT
COSMETICS AND HOUSEHOLD CHEMICAL SUBSTANCES
- ADVERTISEMENT OF DRUGS, COSMETICS, HOUSEHOLD CHEMICALS & MEDICAL DEVICES
- GUIDELINES FOR THE REGISTRATION OF PARALLEL IMPORTED COSMETICS AND HOUSEHOLD CHEMICAL SUBSTANCES
- IMPORTATION OF COSMETICS AND HOUSEHOLD CHEMICAL SUBSTANCES
- REGISTRATION OF COSMETICS AND HOUSEHOLD CHEMICAL SUBSTANCES IN GHANA
- REQUIREMENTS FOR LABELLING OF PRODUCTS
MEDICAL DEVICES
- GUIDELINE FOR REGISTRATION OF MEDICAL DEVICES
- GUIDELINE FOR IMPORTATION OF MEDICAL DEVICES
- MEDICAL DEVICES SAMPLE SCHEDULE
- GUIDELINE FOR DONATION OF MEDICAL DEVICES
- GUIDELINES FOR REGISTRATION OF SOFTWARE AS A MEDICAL DEVICE
- ADVERTISEMENT OF DRUGS, COSMETICS, HOUSEHOLD CHEMICALS & MEDICAL DEVICES
DRUGS REGISTRATION
- GUIDELINES FOR REGISTRATION OF ALLOPATHIC MEDICINES CONSIDERED FOR SMALL SCALE MANUFACTURE
- TIMELINES FOR MEDICINAL PRODUCT REGISTRATION
- TIMELINES FOR MEDICINAL PRODUCT RE-REGISTRATION
- GUIDELINES FOR REGISTRATION OF UK GENERICS
- GUIDELINES FOR IMPORTATION OF DRUGS
- GUIDELINES FOR REGISTRATION OF ALLOPATHIC DRUGS
- GUIDELINES FOR STABILITY TESTING OF ACTIVE PHARMACEUTICAL INGREDIENTS AND FINISHED PHARMACEUTICAL PRODUCTS
- TEMPLATE QUALITY INFORMATION SUMMARY (QIS)
- TEMPLATE QUALITY OVERALL SUMMARY PRODUCT DOSSIER (QOS-PD)
- TEMPLATE LABELLING
- GUIDELINES FOR REGISTRATION OF ALLOPATHIC DRUGS-QUALITY PART
- TEMPLATE PATIENT INFORMATION LEAFLET
- TEMPLATE SUMMARY OF PRODUCT CHARACTERISTICS (SmPC)
- VARIATION GUIDELINES FOR ALLOPATHIC MEDICINES
- GUIDELINES FOR CONDUCTING BIOEQUIVALENCE STUDIES
- GUIDELINES FOR THE REGISTRATION OF MEDICINAL PRODUCTS CLASSIFIED FOR FAST TRACK PROCESSING
- GUIDELINES FOR THE REGISTRATION OF PARALLEL IMPORTED DRUGS OR HERBAL MEDICINAL PRODUCTS
- GUIDELINES FOR REGISTRATION OF VETERINARY NUTRITIONAL/DIETARY SUPPLEMENTS
- GUIDELINES FOR REGISTRATION OF VETERINARY MEDICINAL PRODUCTS
- GUIDELINE FOR DONATION OF DRUGS
- GUIDELINES FOR LABELLING OF DRUGS
- GUIDELINES FOR THE CANCELLATION/ SUSPENSION OF A REGISTERED DRUG
- GUIDELINES FOR REGISTRATION OF AN ORPHAN DRUG
- PRODUCT LITERATURE STANDARD FOR VETERINARY PRODUCTS
DRUGS INDUSTRIAL SUPPORT
