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certain substances for medical and scientific purposes, while preventing their diversion into illicit channels. In the Single Convention on Narcotic Drugs of 1961, as amended by the 1972 Protocol, narcotic drugs and their preparations are essentially listed in four schedules according
This publication is intended to give a brief description of the drugs most frequently manufactured/processed and/or abused, as well as definitions of the most relevant scientific terms used in this context. It is by no means exhaustive, nor is it meant to replace any of the more comprehensive textbooks and encyclopedias on drugs of abuse.
1 Μαρ 2016 · PDF | The UNODC publication Terminology and Information on Drugs introduces basic concepts and materials on substances under international control,... | Find, read and cite all the research...
30 Απρ 2021 · Now in its 37th edition, it is still the ideal first-line reference work and remains a trusted source of information for more detailed drug inquiries. Alongside conventional medicines, information is included on herbals, diagnostic agents, radiopharmaceuticals, pharmaceutical excipients, toxins, and poisons making Martindale your complete ...
WHODrug is a global medicinal information dictionary that contains medicinal products and active ingredients intended for human use, such as active chemical substances, biother-apeutics, vaccines, dietary supplements, herbal remedies, radio pharmaceuticals and diagnostic agents.
Terminology and Information on Drugs: This publication introduces basic concepts and materials on substances under international control, which are most frequently manufactured or processed and/or abused, as well as definitions of scientific terms used in this context.
FDA U.S. Food and Drug Administration (www.fda.gov) Health Canada Federal departmentresponsible for health product regulation in Canada (www.hc-sc.gc.ca) HPRA Health Products Regulatory Authority, Ireland (www.hpra.ie) HSA Health Sciences Authority, Singapore (www.hsa.gov.sg) ICDRA International Conference of Drug Regulatory Authorities
