Pure Global AI
FDA Philippines RA

RA 9711

Republic Act No. 9711 - FDA Act of 2009
PhilippinesFood and Drug AdministrationGeneralEffective August 2009
What this code is

RA 9711 is the official FDA identifier for “Republic Act No. 9711 - FDA Act of 2009”. RA 9711 is the official identifier FDA uses for this instrument.

Instrument
RA
Full name
RA 9711
Category
General
Source links
Authority source
English
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
0 articles · 1 language version
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
18 August 2009
Effective
August 2009
Readable full text

Open a language version

Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

About this regulation

Republic Act No. 9711 - FDA Act of 2009

Republic Act No. 9711, the Food and Drug Administration (FDA) Act of 2009: renames BFAD the FDA and amends RA 3720 across Sections 1-28 — objectives, powers, prohibited acts, penalties, a Regulatory Enforcement Unit, retained income, Congressional oversight, and the effectivity clause. The recorded FDA page URL serves the official gazette-style scan (27 pages) as PDF bytes; the site’s WAF blocks non-browser user agents on that route, so retrieval uses a standard browser UA against the same official URL. Scan OCR artifacts (e.g. "SIX. 9." for "SEC. 9.") are corrected positionally by the parser, not by editing text.

RA 9711 is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.