- Jordanian Food and Drug Administration (JFDA) Official Web
Site:
http://www.jfda.jo/index.aspx
- Clinical Research Law:
http://www.jfda.jo/custom/law/general/7.doc (Arabic version)
http://www.jfda.jo/custom/law/23.doc (English version)
- FDA Information Sheet Guidances for Institutional Review
Boards, Clinical Investigators, and Sponsors:
http://www.fda.gov/oc/ohrt/irbs/default.htm
- Guidance for Clinical Trial Sponsors: Establishment and
Operation of Clinical Trial Data Monitoring committees:
http://www.fda.gov/OHRMS/DOCKETS/98fr/01d-0489-
gdl0003.pdf
- Guidance for Industry: Guideline for the Monitoring of
Clinical Investigators:
http://www.fda.gov/ora/compliance_ref/bimo/clinguid.html
- ICH E6 Good Clinical Practice Consolidated Guidance:
http://www.fda.gov/cder/guidance/959fnl.pdf
- ICH E3: Guideline for Industry Structure and Content of
Clinical Study Reports:
http://www.fda.gov/cder/guidance/iche3.pdf
- Declaration of Helsinki:
http://www.rotrf.org/information/Helsinki_declaration.pdf
- Organisation for Economic Co-operation and Development
(OECD) Principles of Good Laboratory Practice (GLP)
http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-
7/a/7ag4a.pdf