Ministry of Health
Department of Health (Philippines)
Regulatory Authority
Food and Drug Administration, Philippines
Medical Device Regulation
Administrative Order 2018-0002
Official Language
Filipino, English
Classification
Class A, B, C, D
Registration Process
Documents Required
Applicable QMS
ISO 13485:2016
Registration Timeline
6-9 months
Authorized Representative
Yes
License Validity
5 years
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
To launch a medical device in a country, medical devices must comply with the local country’s regulatory requirements. Let us be your trusted partner in bringing your medical devices to the Global market. Contact us today to learn more about how we can assist you in every step of the way.
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