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