Legal Status of Traditional Medicine and Complementary/Alternative Medicine: A Worldwide Review
(2001; 200 pages) View the PDF document
Table of Contents
View the documentAcknowledgements
View the documentForeword
Open this folder and view contentsIntroduction
Open this folder and view contentsAfrica
Close this folderThe Americas
View the documentArgentina
View the documentBolivia
View the documentBrazil
View the documentCanada
View the documentChile
View the documentColombia
View the documentCosta Rica
View the documentCuba
View the documentDominican Republic
View the documentEcuador
View the documentGuatemala
View the documentHonduras
View the documentJamaica
View the documentMexico
View the documentNicaragua
View the documentPanama
View the documentPeru
View the documentUnited States of America
View the documentVenezuela
Open this folder and view contentsEastern Mediterranean
Open this folder and view contentsEurope
Open this folder and view contentsSouth-East Asia
Open this folder and view contentsWestern Pacific
View the documentReferences
Open this folder and view contentsAnnex I. The European Union
 

Jamaica

Statistics

More than 8000 medicinal products, including 610 vitamins, 90 minerals, and 60 herbal remedies, were registered and licensed in Jamaica between 1975 and 2000. Of the 403 medicinal products registered in 1999, 9.5% were of herbal origin (132). Herbal products are a multi-million dollar industry in Jamaica (133).

Regulatory situation

In 2000, the Parliament considered revisions to the Food and Drugs Act of 1964 and the Food and Drugs Regulations of 1974. The revisions (134) were aimed at ensuring the safety, efficacy, and quality control of herbal products. In 2001, the Parliament approved the revisions, under which the following applied:

• Products are subject to approval, requirements for which are similar to, but not as elaborate as, those for pharmaceuticals. The onus is on manufacturers to substantiate quality, efficacy, and safety.

• Products containing vitamins and minerals in less than three times the recommended daily amount are classified as foods and do not require formal registration.

• Vitamins containing more than three times the recommended daily amount are classified as drugs.

• Herbal products require registration if they contain substances used for conditions that normally need medical intervention.

• Herbal products containing substances used for self-limiting conditions that do not normally require medical intervention do not require registration.

• Registered products, like drugs, require a permit for importation.

• Products that are not registered do not require a permit for importation; however, proof of quality is required annually or such other time, as deemed necessary.

The revisions define an herbal medicine as "a medicinal product consisting of a substance produced by subjecting a plant or plants to drying, crushing, or any other process or of a mixture whose sole ingredients are two or more substances so produced or of a mixture whose sole ingredients are one or more substances so produced and water or some other inert substance". This definition is adapted from Section 132 of the United Kingdom's Medicines-Act of 1968.

There is no chiropractic law. Chiropractors are recognized as medical practitioners but prohibited from providing physical therapy services and from using the title of "Doctor".

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Last updated: May 3, 2013