British Pharmacopoeia (BP)
http://www.pharmacopoeia.org.uk
Canadian HPFB Inspectorate
http://www.hc-sc.gc.ca/hpfb-dgpsa/inspectorate/index_e.html
European Chemical Industry Council – Active Pharmaceutical Ingredients Sector (CEFIC/APIC)
http://apic.cefic.org
The European Commission DG Enterprise
http://europa.eu.int/comm/enterprise/pharmaceuticals/index_en.htm
European Compilation of Procedures for GMP Inspections
http://www.emea.eu.int/Inspections/docs/335103en.doc
European Federation of Pharmaceutical Industries and Federations (EFPIA)
http://www.efpia.org
European Guide to GMP
http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/homev4.htm
European Guide to GMP – updates etc
http://ec.europa.eu/enterprise/pharmaceuticals/pharmacos/gmp_doc.htm
European Guidelines on Quality, Safety, and Efficacy
http://www.emea.eu.int/sitemap.htm
European Medicines Agency (EMEA)
http://www.emea.europa.eu
European Medicines Agency Inspections Sector
http://www.emea.eu.int/Inspections/index.html
European Pharmacopoeia (EP)
http://www.pheur.org
Food and Drug Administration (FDA)
http://www.fda.gov
FDA CBER Guidance / Guidelines / Points to Consider
http://www.fda.gov/cber/guidelines.htm
FDA GMP Regulations (CFR21)
http://www.access.gpo.gov/nara/cfr/waisidx_01/21cfr211_01.html
FDA Inspections Operations Manual
http://www.fda.gov/ora/inspect_ref/iom/iomtc.html
FDA Inspection Guides
http://www.fda.gov/ora/inspect_ref/igs/iglist.html
FDA portal providing access to the different parts of their website
http://www.fda.gov/oc/industry/default.htm
Good Automated Manufacturing Practice (GAMP)
http://www.ispe.org/gamp
Health Sciences Authority (HSA) – Singapore
http://www.hsa.gov.sg
International Conference on Harmonisation (ICH)
http://www.ich.org/UrlGrpServer.jser?@_ID=276&@_TEMPLATE=254
International Pharmaceutical Excipients Council (IPEC)
http://www.ipec.org
International Pharmaceutical Federation (FIP)
http://www.fip.nl
International Society for Pharmaceutical Engineers (ISPE)
http://www.ispe.org
Irish Medicines Board (IMB)
http://www.imb.ie
Japanese Ministry of Health, Labor and Welfare (MHW)
http://www.mhlw.go.jp/english
Malaysian National Pharmaceutical Control Board (NPCB)
http://www.bpfk.gov.my
Medical Device Link
http://www.devicelink.com
Mutual Recognition Agreements (MRAs)
http://www.emea.eu.int/Inspections/MRA.html
The Parenteral Society – UK
http://www.parenteral.org.uk
Pharmaceutical Inspection Cooperation Scheme (PIC/S)
http://www.picscheme.org/index.htm
Pharmaceutical Online
http://www.pharmaceuticalonline.com
Pharmaceutical and Research Manufacturers of America (PhRMA)
http://www.phrma.org
The Pharmaceutical Quality Group (PQG)
http://www.pqg.org
Pharmacos Enterprise DG
http://pharmacos.eudra.org
PharmWeb
http://www.pharmweb.net
Regsource – Regulatory Information
http://www.regsource.com
Risk-Based Approach to Pharmaceutical Current Good Manufacturing Practices (cGMP) for the 21st Century – Table of Contents
http://www.fda.gov/cder/gmp/gmp2004/GMP_finalreport2004.htm
Therapeutic Goods Administration (TGA) – Australia
http://www.tga.gov.au
Therapeutic Products Directorate – Canada
http://www.hc-sc.gc.ca/hpfb-dgpsa/tpd-dpt
UK Medicines and Healthcare Products Regulatory Agency (MHRA)
http://www.mhra.gov.uk
UK Official Documents including the “Orange Guide” and Medicines Legislation
http://www.tso.co.uk/bookshop/bookstore.asp
United States Pharmacopoeia (USP)
http://www.usp.org
World Health Organisation GMP Information (WHO)
http://www.who.int/medicines/areas/quality_safety/quality_assurance/production/en/index.html
World Pharma Web
http://www.worldpharmaweb.com
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