The following list is not complete and based on best current know-how. Therefore

thanks for indicating us valuable links to regulatory bodies!

Quality guidelines

Substances that may be used in Listed medicines in Australia - December 2007

Draft Resolution on GMP for Excipients - 28 May 2012

http://www.cir-safety.org/ingredients

European association with regard to pharmaceutical Quality Assurance and GMP compliance

European Medicines Agency - Quality - Excipients

Draft Guideline on the use of phthalates as excipients in human - 25 April 2013

Guideline on excipients in the dossier for application for
marketing authorization of a medicinal product - June 2007

Excipients in the label and package leaflet of medicinal products for human use - July 2003

STEP Database

List of certified companies

EXCiPACT-Standards

Drug Master File List

Meetings between FDA and the International Pharmaceutical Excipients Council (IPEC)

Inactive Ingredient Search for Approved Drug Products

Generally Recognized as Safe (GRAS)

http://www.finnbrit.com/SubPages/Excipients/regulatory.html

http://www.gelatine.org/en/applications/gelatine/pharma.html

http://www.pharmpress.com/product/9780857110275/excipients

Homepage

Excipient Qualification Guide (2008)

Meetings between FDA and the International Pharmaceutical Excipients Council (IPEC)

List of Acronyms

Regulatory Reference

http://www.ipec-china.org/EnAboutUs.asp?ID=1

Guidelines

Excipact

http://www.jpec.gr.jp/english/

Japanese Pharmacopiea

Ministry of Food and Drug Safety

http://www.who.int/medicines/areas/quality_safety/regulation_legislation/list_mra_websites_nov2012.pdf?ua=1