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    12. Resources (listed in descending order of precedence)
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    Contents

    12. Resources (listed in descending order of precedence)

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    Article summary

    1. Sueblinwong T, Mahaisavariya P and Panichkul S (2007) The Ethical Guidelines for Research on Human Subject in Thailand, 2007, Forum for Ethical Review in Thailand
    2. RegDesk (16 November 2020) Thailand FDA on Direct Advertising and Labelling, RegDesk
    3. Baker McKenzie (n.d.) Global Data Privacy & Security Handbook – Thailand, Baker McKenzie
    4. DocuSign (n.d.) eSignature Legality in Thailand, Docusign
    5. Food and Drug Administration (FDA) (2020), COVID-19, FDA
    6. International Council for Harmonisation ICH (9 November 2016) Integrated Addendum to ICH E6(R1): Guideline for Good Clinical Practice, ICH
    7. Food and Drug Administration (FDA)(n.d.) Submission of Supporting Documents for Approval via Electronic Means (SKYNET Smart Drop box), FDA
    8. Food and Drug Administration (FDA) Guideline on Submission of Application for Drug Import Permit into Thailand for Clinical Trial, International Affairs and Investigational Drug Section
    9. Central Research Ethics Committee (CREC)(n.d.) HomePage, CREC
    10. Thai Clinical Trials Registry (TCTR)(n.d.) HomePage, TCTR
    11. Credevo (12 September 2021) Clinical Trial Regulatory & Approval Process in Thailand (Part-1), Credevo
    12. Food and Drug Administration Thailand (FDA) Welcome to FDA Thailand, FDA
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