Training on IVDMD Regulatory Frameworks, Selection, Assessment and Validation
Training on IVDMD Regulatory Frameworks, Selection, Assessment and Validation
Date Posted: March 11, 2025. Link to Post: bit.ly/hfdb-gppa-25010
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HFDB GPPA Code: HFDB-Q1-20250311-010
FULL TITLE OF GPPA: Training on In-Vitro Diagnostic Medical Devices (IVDMD) Regulatory Frameworks, Selection, Assessment and Validation
DESCRIPTION: This activity aims to provide a comprehensive understanding of IVDMD regulation, including its scope and basics, principles of classification, and examples of regulatory practices. Participants shall develop skills to draft IVDMD regulation documents, create action plans for implementation, and understand key concepts and terms used in IVDMD assessment and validation procedures. (Reference: Department Personnel Order No. 2025-1370, "Authority for Selected Officials and Personnel of the Department of Health (DOH) Central Office, National Reference Laboratory, and Food and Drug Administration to Attend the Training on IVDMD Regulatory Frameworks, Selection, Assessment and Validation on March 24-27, 2025 in Bayview Park Hotel, Manila" dated March 4, 2025)
STATUS AS OF THIS POST: Ongoing
RESPONSIBLE HFDB UNIT: OHL
For particulars or complaints about this project, please contact the Regional Office or Cluster which has audit jurisdiction on this project:
COA Cluster 6 - Health and Science
Address: Commonwealth Avenue, Quezon City, contact no. (02) 8952-4978 Ext. 5006 or 5023, text COA Citizen's Desk at (0917) 320-6543, or email at citizensdesk@coa.gov.ph
COA Cluster 6 - Health and Science
Address: Commonwealth Avenue, Quezon City, contact no. (02) 8952-4978 Ext. 5006 or 5023, text COA Citizen's Desk at (0917) 320-6543, or email at citizensdesk@coa.gov.ph
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