Draft for Comments || Guidelines on the Filing and Submission of Applications for the Licensing of Household/Urban Hazardous Substances (HUHS) Establishments through the Food and Drug Administration (FDA) eServices Portal System
The Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) is soliciting comments on the proposed FDA Circular, provisionally entitled, “Guidelines on the Filing and Submission of Applications […]
Draft for Comments || Recognition of Accredited Technical Service Providers for Radiation Dosimetry of Individual Monitoring Services
All comments and recommendations shall be sent as a *.docx or *.pdf to [email protected]. The comment sheet may be accessed through the following link: http://wf26.2.vu/tsprecog/ I. BACKGROUND The Food and […]
Draft for Comments || Guidelines for the Notification of All Importation and Exportation of Finished Drug Products and Raw Materials
All comments may be sent to [email protected]. The deadline for submission of comments is on 25 August 2023. I. RATIONALE Republic Act (RA) No. 9711, otherwise known as the […]
Draft for Comments || Application Process and Requirements for Post-Approval Changes of Biological Products Adopting the World Health Organization Guidelines for Changes to Approved Vaccines and Biotherapeutic Products for Human Use
The extended deadline for submission of comments is until 22 August 2023. All comments may be sent at [email protected]. I. BACKGROUND By virtue of Administrative Order (A.O.) No. 47-a, […]
Draft for Comments || Rules and Regulations for Establishment and Operation of Medical Magnetic Resonance Imaging (MRI) Facilities in the Philippines
All comments may be sent at [email protected]. The deadline for submission of comments is on 14 August 2023. Attachments Draft_AO_ Rules and Regulations for Establishment and Operation of Medical Magnetic […]
Draft for Comments || Rules and Regulations on the Issuance of Authorization for Registration Applications of Drug Products and Drug Substances by the Food and Drug Administration
All comments may be sent at [email protected]. The deadline for submission of comments is on 31 July 2023. Comment Form Word File >> https://bit.ly/43m51qr I. BACKGROUND Article II, Section 15, of the […]
Draft for Comments || Guidelines on the Publishing of Package Insert and Patient Information Leaflet of Registered Drug Products in the Food and Drug Administration (FDA) Verification Portal System
All comments may be sent at [email protected]. The deadline for submission of comments is on 7 July 2023. I. BACKGROUND Article I Section 2 of the Implementing Rules and […]
Draft for Comments || Updated Guidelines on the Application for License to Operate of Health Product Establishments with the Food and Drug Administration
All concerned stakeholders may submit comments in MS word format via email to [email protected], copy furnish [email protected]. The deadline for submission of comment is on 30 June 2023. I. RATIONALE […]
Draft for Comments || Guidelines for the Importation and Exportation of Finished Drug Products and Raw Materials
All comments may be sent at [email protected]. The deadline for submission of comments is on 23 June 2023. I. RATIONALE Republic Act (RA) No. 9711, otherwise known as the “Food […]
Draft for Comments || Submission of Comments on the Draft Philippines National Standard (PNS) and Recommended Code of Practice (RCP) for Peanut Butter by the Center for Food Regulation and Research (CFRR)
All concerned stakeholders may submit comments in MSWord format via email to [email protected] on or before 19 May 2023 using the format attached. Attachments PNS Peanut Butter (520 […]