FDA 
Proposed Halal 
Plans or Program 
Terms of Reference
Outline 
 FDA Mandate 
 FDA TOR 
 Licensing 
 Registration 
 Post-market Surveillance
FDA-Regulated Products 
 Processed Food, Food Additives, Food 
Supplements and other Food Products 
 Cosmetic Products, Tobacco 
 Pharmaceutical Products (Human and 
Animals, Biological Products) 
 Medical Devices, Radiation-emitting 
equipment/devices 
 Others – Toys, Urban Pesticides, etc
FDA Terms of Reference 
(Halal) 
Licensing of Establishment 
Product Registration 
Post-Market Surveillance
FDA Initiatives on Halal 
 Creation of Halal Unit 
 To support the Halal industry (for health products) in 
the country with the other agencies, led by the NCMF 
 To ensure truthfulness of Halal claims in relation to 
issuance of Licensing of Establishments (LTO), Product 
Registration (CPR/Product Notification), and Post-market 
Surveillance of establishments and products 
(e.g. audits, sampling and testing of products for Halal) 
 To ensure that FDA health product policies or guidelines 
on Halal are consistent with the Philippine National 
Standards and national policy on Halal
Licensing 
(Health products-Food, Cosmetic, Pharmaceutical and Medical 
Devices) 
 FDA shall issue LTO to Manufacturers (cGMP) first 
before the establishment can apply for Halal 
certification issued by NCMF-accredited Halal 
Certifying Body (proposal) 
 Consistent with the TESDA plan to conduct 
Training on Halal, establishments that are Halal-certified 
shall employ TESDA-trained on Halal 
personnel
Registration 
(Health Products - Food, Cosmetics, Pharmaceuticals and Medical 
Devices) 
 All Halal label claims shall be substantiated 
by a Certification/Certificate issued by a 
Halal-certifying body recognized by NCMF 
 The FDA shall issue specific requirements or 
guidelines on how the Halal claim shall be 
substantiated, or to address any gaps fro clarity 
and consistency with the policies or guidelines 
NCMF or other agencies. (proposal)
Post-Market Surveillance 
(Health products – Food, Cosmetics, Pharmaceuticals) 
 Laboratories engaged in testing health products for 
Halal shall be required FDA-lab accreditation (RA 9711) 
 Halal laboratory certificates issued by FDA-accredited 
laboratories or laboratories recognized by the NCMF or 
Halal-certifying bodies shall be accepted by the FDA for 
regulatory purposes, e.g. licensing, registration and 
PMS 
 Develop FDA laboratory to test Halal health products 
(proposal) to act as a 3rd-party lab for the industry and 
independent laboratories
Challenges 
 Clear policy, rules and regulations issued by interagency committed on 
Halal, led by NCMF; FDA Circulars/Memos issued by the FDA shall be 
subjected to public consultation and public hearing, and the concurrence 
by the NCMF shall be sought out. 
 There is a Philippine National Standard (PNS) on Halal Food, but no PNS 
for Cosmetics, Pharmaceutical Products and Medical Devices 
 No application for FDA-accreditation for Halal laboratory (or under scope 
of test) has yet been received by the FDA. There is a need for capacity 
building on testing Halal. 
 Coordination with the DA NMIS/BAI in implementing PNS or FDA policies on 
Halal Food 
 Employment of FDA evaluators, analysts and inspectors, among other 
personnel, who are Muslim for effective implementation of rules and 
regulation on Halal
Thank you for listening 
Prepared by: 
NIDA G. ESCALO, RPH 
Food-Drug Regulation Officer V 
Policy and Planning Office 
For comments or suggestions, please call/email: 
Phone: (+63) 857 1900 loc 1121 
Email: ngescalo@fda.gov.ph

Fda

  • 1.
    FDA Proposed Halal Plans or Program Terms of Reference
  • 2.
    Outline  FDAMandate  FDA TOR  Licensing  Registration  Post-market Surveillance
  • 3.
    FDA-Regulated Products Processed Food, Food Additives, Food Supplements and other Food Products  Cosmetic Products, Tobacco  Pharmaceutical Products (Human and Animals, Biological Products)  Medical Devices, Radiation-emitting equipment/devices  Others – Toys, Urban Pesticides, etc
  • 4.
    FDA Terms ofReference (Halal) Licensing of Establishment Product Registration Post-Market Surveillance
  • 5.
    FDA Initiatives onHalal  Creation of Halal Unit  To support the Halal industry (for health products) in the country with the other agencies, led by the NCMF  To ensure truthfulness of Halal claims in relation to issuance of Licensing of Establishments (LTO), Product Registration (CPR/Product Notification), and Post-market Surveillance of establishments and products (e.g. audits, sampling and testing of products for Halal)  To ensure that FDA health product policies or guidelines on Halal are consistent with the Philippine National Standards and national policy on Halal
  • 6.
    Licensing (Health products-Food,Cosmetic, Pharmaceutical and Medical Devices)  FDA shall issue LTO to Manufacturers (cGMP) first before the establishment can apply for Halal certification issued by NCMF-accredited Halal Certifying Body (proposal)  Consistent with the TESDA plan to conduct Training on Halal, establishments that are Halal-certified shall employ TESDA-trained on Halal personnel
  • 7.
    Registration (Health Products- Food, Cosmetics, Pharmaceuticals and Medical Devices)  All Halal label claims shall be substantiated by a Certification/Certificate issued by a Halal-certifying body recognized by NCMF  The FDA shall issue specific requirements or guidelines on how the Halal claim shall be substantiated, or to address any gaps fro clarity and consistency with the policies or guidelines NCMF or other agencies. (proposal)
  • 8.
    Post-Market Surveillance (Healthproducts – Food, Cosmetics, Pharmaceuticals)  Laboratories engaged in testing health products for Halal shall be required FDA-lab accreditation (RA 9711)  Halal laboratory certificates issued by FDA-accredited laboratories or laboratories recognized by the NCMF or Halal-certifying bodies shall be accepted by the FDA for regulatory purposes, e.g. licensing, registration and PMS  Develop FDA laboratory to test Halal health products (proposal) to act as a 3rd-party lab for the industry and independent laboratories
  • 9.
    Challenges  Clearpolicy, rules and regulations issued by interagency committed on Halal, led by NCMF; FDA Circulars/Memos issued by the FDA shall be subjected to public consultation and public hearing, and the concurrence by the NCMF shall be sought out.  There is a Philippine National Standard (PNS) on Halal Food, but no PNS for Cosmetics, Pharmaceutical Products and Medical Devices  No application for FDA-accreditation for Halal laboratory (or under scope of test) has yet been received by the FDA. There is a need for capacity building on testing Halal.  Coordination with the DA NMIS/BAI in implementing PNS or FDA policies on Halal Food  Employment of FDA evaluators, analysts and inspectors, among other personnel, who are Muslim for effective implementation of rules and regulation on Halal
  • 10.
    Thank you forlistening Prepared by: NIDA G. ESCALO, RPH Food-Drug Regulation Officer V Policy and Planning Office For comments or suggestions, please call/email: Phone: (+63) 857 1900 loc 1121 Email: ngescalo@fda.gov.ph