Free Useful Info



 SCIENTIFIC LITERATURE SEARCH

  1. Pubmed/Medline: Free US National Library of Medicine database of references.
  2. Science Direct : An online books and journals resource.
  3. Scirus : Scientific research tool.
  4. Toxnet : Databases on toxicology, hazardous chemicals, environmental health and toxic release.
  5. Embase : Biomedical Answers.
  6. Doaj : Directory of open access journals.
  7. Springer : International publisher science, technology, and medicine subjects.
  8. Wiley: Online Library
  9. Scopus : Scientific, technical, medical, and social science literature.
  10. Ojose: Online journal search engine.
  11. Meta press: Metapress hosting services for academic publishers.
  12. High Wire : Free full text Science search.
  13. Karger : Connecting the world of biomedical science.
  14. Emerald : Advance search results on all the subjects.
  15. Web of science : Intellectual Property and science search.
  16. Cochrane : To provide the best evidence for health care.
  17. Thieme : Resources for students
  18. Sage: Publisher of books and journal in india and south asia.
  19. Medworm : Pharmacy, Medical and health related articles.
GUIDANCE DOCUMENTS AND INFORMATION
  1. ICH Guidelines : International conference on harmonisation guidelines.
  2. WHO Guidelines : World health organization guidelines.
  3. IPEC Guidelines: The international pharmaceutical excipients  council europe.
  4. PIC/S: The pharmaceutical inspection convention and pharmaceutical inspection co-operation scheme.
  5. EMA:  Europe medicines agency
  6. European Commission: Medicinal products for human and veterinary use.
  7. PAHO: Pan Americal health organization.
  8. 21 CFR Part 210: Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs (General)
  9. 21 CFR 211: Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs; Current good manufacturing practice for finished pharmaceuticals.
  10. 21 CFR 58: Good laboratory practice for non-clinical laboratory studies.
  11. 21 CFR 600 : Biological products in general.
  12. 21 CFR 601: Licensing.
  13. 21 CFR 610: General biological products standards.
  14. 21 CFR 606: CGMP for blood and blood components
  15. FDA: Food and drug administration.
  16. TGA: Therapeutic goods administraion.
  17. Heath Canada: Guidelines
  18. CDSCO: Central drugs standard control orgainzation.
  19. MHRA: Medicine and heath care products regulatory agency.
  20. PMDA: Pharmaceuticals and medical devices agency, Japan.
  21. MEDSAFE: New Zealand medicines and medical devices safety authority.  
PHARMACIST ZONE




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“Knowledge Grows When Shared” is my belief and hence this blog. It would be wonderful if the visitors to this blog too can contribute by answering to questions posed. Not all the questions here have an answer from me but we together can create a veritable pool of knowledge here. Thank you