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Australia herbal products

Some regulatory authorities have foreseen the future impact of TM and set up appropriate guidelines. The European Union has legislation for traditional herbal products. Another example is the Therapeutic Goods Administration of Australia, which has set up a complementary medicine section that controls the regulatory practices for TM. [Pg.365]

In Venezuela, there is no official fast-track system. However, brief-mode registration is available for generic products for which a bioavailabilily study has been undertaken. Similarly, Malaysia has an abridged procedure for registration of products classified as non-scheduled poisons. This type of simplified procedure does not, in essence, differ from the use of less stringent registration requirements for certain categories of products as seen, for example, for herbal medicines in Australia and the Netherlands. [Pg.75]

Each of the countries operates a quality analysis system for post-marketing control of drug quality, albeit with vast differences in capacity. Data on the outcome measure for drug quality— the number of dmg samples that failed quality tests compared with the total number of samples collected— are available in all the countries, except the Netherlands. Failure rates are high in some countries, e.g. Tunisia and Uganda. In Australia, high failure rates are found for herbal and other complementary products, compared with prescription dmgs. Empirical data on sanctions applied in such instances are not available. [Pg.123]

Whitten, G. Herbal Harvest - commercial organic production of quality and dried herbs, Bloomingham Books, Australia, 1997. [Pg.360]


See other pages where Australia herbal products is mentioned: [Pg.74]    [Pg.887]    [Pg.228]    [Pg.258]    [Pg.4468]    [Pg.53]    [Pg.73]    [Pg.122]    [Pg.4]    [Pg.366]    [Pg.204]    [Pg.18]    [Pg.74]    [Pg.233]    [Pg.235]    [Pg.24]    [Pg.26]    [Pg.33]    [Pg.43]    [Pg.118]    [Pg.42]    [Pg.369]   
See also in sourсe #XX -- [ Pg.213 ]




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