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- 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

 
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