Fdaghana.gov.gh

Welcome to Ghana Food And Drugs Authority Home

WebThe Division's mandate as derived from Part 6, 7 & 8 of the Public Health Act 2012, Act 851, is to protect public health and safety by ensuring the availability of safe, efficacious and quality allopathic medicines, veterinary medicines, vaccines, biological products, tobacco & tobacco products, herbal medicines, homoeopathic medicines, food

Actived: 8 days ago

URL: http://www.fdaghana.gov.gh/drug-registration.php

Navrongo Health Research Centre (NHRC) Site Profile

WebNavrongo Health Research Centre (NHRC) Site Profile The NHRC is one of three research centres of the Research and Development Division of the Ghana

Category: Health Go Health

Welcome to Ghana Food And Drugs Authority Home

WebThe FDA was formally mandated by the Food and Drugs Law of 1992, PNDCL 305B and its amendment, Act 523. In 2012, this law was reviewed and the Public Health Act (PHA) 2012, Act 851 was passed to increase the scope and enhance public health and safety. Part 8, Sections 150-166 of the PHA 2012, Act 851 mandates the FDA to regulate Clinical Trials.

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Welcome to Ghana Food And Drugs Authority Home

WebFunctions of the Authority. Ensure adequate and effective standards for food, drugs, cosmetics, household chemicals and medical devices Monitor through the District Assemblies and any other agency of State compliance with the provisions of Part 6, 7 and 8 of the Public Health Act, 2012 (ACT 851) Advise the Minister on measures for the …

Category: Food, Medical Go Health

NATIONAL FOOD SAFETY POLICY

Web11. 13. Policy objective 1: To strengthen food safety governance in Ghana 13. Policy objective 2: Strengthen institutional coordination and collaboration. 14. Policy objective 3: To promote and ensure harmonization, synergy and enforcementof laws and regulation on food safety in Ghana.

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CODE OF HYGIENIC PRACTICE FOR FOOD SERVICE …

WebFDA/ FSMD/CP-FSE/2013/03 Page 1 of 28 FOOD AND DRUGS AUTHORITY CODE OF HYGIENIC PRACTICE FOR FOOD SERVICE ESTABLISHMENT IN THE HOSPITALITY INDUSTRY Document No.: FDA/ FSMD/CP-FSE/2013/03 Date of First Adoption: 1st February 2013 Date of Issue: 1st March 2013 Version No.: 01

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Ministry of Health/Ghana Health Service Guidelines for …

Web1 Ministry of Health/Ghana Health Service Guidelines for International Flight Operations on COVID-19 Safety at the Kotoka International Airport

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FOOD AND DRUGS AUTHORITY 2021 ANNUAL REPORT

WebPage 4 of 46 EXECUTIVE SUMMARY The Food and Drugs Authority (FDA) is the national regulatory agency in Ghana mandated by Parts 6, 7 and 8 of the Public Health Act, 2012 (Act 851) to assure the safety, quality and

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Vaccines in the EPI schedule of Ghana

WebVaccines in the EPI schedule of Ghana The Expanded Programme on immunisation (EPI) was launched in 1974 by the World Health Organisation (WHO) and adopted by Ghana in 1978.

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The Pharmacovigilance System in Ghana

Web2 Reporting Programmes4,5 and Patient Safety Centre, an initiative undertaken in collaboration with community pharmacies. There is also a programme in collaboration with the Ghana Health Service to peer review pharmacovigilance performance of health

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GUIDELINE FOR REGISTRATION OF MEDICAL DEVICE

Webfood and drugs authority doc. type: guideline doc no.: fda/mdd/gl-01 page 1 of 59 rev. no.: 02 title: guideline for registration of medical device

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Recommended routine immunization

WebReference: Modified from World Health Organization (WHO) Date accessed: 29 March 2018 NATIONAL IMMUNIZATION SCHEDULE Ghana Recommended routine immunization

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FOOD AND DRUGS AUTHORITY 2020 ANNUAL REPORT

WebPage 5 of 37 EXECUTIVE SUMMARY The Food and Drugs Authority (FDA) is the national regulatory body in Ghana mandated by Parts 6, 7 and 8 of the Public Health Act, 2012 (Act 851) to assure the safety, quality and

Category: Food Go Health

REGULATION OF CLINICAL TRIALS IN GHANA Scope

WebFDA Clinical Trials Application Guide b) The Authority has issued a final Clinical Trial Authorization certificate c) The Principal Investigator is resident in Ghana.

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FOR IMMEDIATE RELEASE PRESS RELEASE

WebPage 2 of 2 The Authority wishes to assure the general public that it remains committed to protect the health and safety of consumers. To this end, the public is admonished to report any

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FOOD AND DRUGS AUTHORITY

Web2. INTERPRETATION. In this guideline, unless the context otherwise states: -. “AUTHORITY” means Food and Drugs Authority. “PRODUCT” means Herbal medicinal product. “APPLICANT” means the product owner or license holder. Representatives of license holders may not hold themselves as applicants unless they own the product.

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FOOD AND DRUGS AUTHORITY

WebPage 1 of 66 1.0 INTRODUCTION In pursuance of the Public Health Act, 2012, Act 851, Part 8, 150-166, these Guidelines are hereby made by the Food and Drugs Authority, hereafter referred to as The Authority, to define the general norms and scientific principles and to set applicable standards for the conduct, performance and control of clinical trials …

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