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Health registration regulations

The quality specifications will be those contained in the official texts cited in Art. 42 of this regulation or those which have been specified in the monographs accepted in granting the health registration, without prejudice of their modification whenever this should be necessary, however. [Pg.342]

This Act has been much amended and now forms a relevant statutory provision for the Health and Safety at Work, etc. Act 1974. Originally it provided for the registration and control of certain classes of chemical works. The Act has now been amended and the classes of premises, the scheduled works , are now included in the Health and Safety (Emission into Atmosphere) Regulations 1983 (amended 1989). There are 62 main categories of works, and in some cases only certain processes within a category are covered ... [Pg.754]

Control of Pollution Act 1974, 519 Control of Pollution (Amendment) Act 1989, 519 Control of Substances Hazardous to Health Regulations 1999, 1, 12, 112, 119, 137, 141 Control of Waste (Registration of Carriers and Seizure of Vehicles) Regulations 1991, 519 Conversion tables, 543 Copper, 30, 274... [Pg.601]

The conduct of clinical trials is regulated in all the countries, except Cypms. In Cypms, the policy of the Ministry of Health is not to permit clinical trials for experimental medical products. Multicountry clinical trials for products licensed in developed countries are undertaken in some institutions and regulated by ethics committees (Table 8.5). In these countries, approval of clinical trials is carried out either by the DRA, as in Estonia, Malaysia, Tunisia, Venezuela and Zimbabwe, or by ethics committees. When the DRA itself is responsible for control, information about the trials is processed centrally. In Tunisia, clinical trials form part of the registration process. Trials are requested, when deemed necessary, by the specialized committee charged with reviewing the new dmg. The trial proposal is then evaluated by the technical committee, and forwarded to the Health Minister for final approval. Cuba has a National Centre for the Coordination of... [Pg.93]

US Environmental Protection Agency (2009) Cyphenothrin. Human health assessment scoping document in support of registration review, EPA-HQ-OPP-2009-0842-0002. http //www. regulations.gov/ documentDetail D=EPA-HQ-OPP-2009-0842-0002. Accessed 15 Feb 2011... [Pg.103]

Hill S, Johnson K. Emerging challenges and opportunities in drug registration and regulation in developing countries. London Health Systems Resource Centre 2004. [Pg.35]

Regulation requiring pre-market registration of products has been indicted in the literature as a major negative factor on innovation. In addition, there is data that these regulations have actually created safety and health problems. [Pg.37]


See other pages where Health registration regulations is mentioned: [Pg.2604]    [Pg.2604]    [Pg.137]    [Pg.141]    [Pg.85]    [Pg.122]    [Pg.404]    [Pg.328]    [Pg.177]    [Pg.30]    [Pg.33]    [Pg.43]    [Pg.129]    [Pg.130]    [Pg.134]    [Pg.29]    [Pg.27]    [Pg.251]    [Pg.214]    [Pg.17]    [Pg.406]    [Pg.19]    [Pg.247]    [Pg.452]    [Pg.5]    [Pg.270]    [Pg.74]    [Pg.69]    [Pg.69]    [Pg.74]    [Pg.77]    [Pg.223]    [Pg.346]    [Pg.476]    [Pg.522]    [Pg.85]    [Pg.122]    [Pg.74]    [Pg.8]    [Pg.62]    [Pg.331]    [Pg.393]   
See also in sourсe #XX -- [ Pg.2604 ]




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Health Regulations

Registration

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