International Ethical Guidelines for Health Related Research Involving Humans(CIOMS 2016)
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ICH Harmonised Guideline -Guideline for Good Clinical Practice_E6(R3)_06 January 2025
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WHO_Operational Guidelines for Ethics Committees that Review Biomedical Research
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WHO_Standards and Operational Guidance for Ethics Review of Health-Related Research with Human Participants
PHREB Policies and Requirements for Accreditation_v1_10
PHREB SOP Workbook 2020
SIDCER-FERCAP Survey Terms of Reference and SOP
SIDCER Recognition Requirements and Process
PHREB Resolution on COVID-19 Research proposals
DOH DO2017-0265 Streamling Ethics Review
DOH AO2020-0010-Regulations on the Conduct of Clinical Trials for Investigational Products
DOH AO2019-0049 SJREB
Implementing Rules and Regulations of Republic Act No.10173, known as the “Data Privacy Act of 2012”
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DOH AO2020-0010 Regulations on the Conduct of Clinical Trials for Investigational Products
DOH AO2018-002 Guidelines Governing the Issuance of an Authorization for a Medical Device based on the ASEAN Harmonized Technical Requirements
FDA Circular No. 2016-019-Revise Guidelines on submission of Equivalence Evidence for Registration of Pharmaceutical Products
FDA Circular No. 2016-017-Additional Post-Approval changes for Pharmaceutical Products
FC2021-002 Medical Devices Implementation
FC2020-001-A Medical Devices Classifications
FC2020-029-1 Applications COVID 19 Trials