FDA Philippines VigilanceVigilance Guidelines
Medical Device Vigilance and Post-Market Surveillance
PhilippinesFood and Drug AdministrationVigilanceEffective 2018
What this code is
Vigilance Guidelines is the official FDA identifier for “Medical Device Vigilance and Post-Market Surveillance”. Vigilance Guidelines is the official identifier FDA uses for this instrument.
- Instrument
- Vigilance
- Full name
- Vigilance Guidelines
- Category
- Vigilance
Source links
- Authority source
- English
- Readable HTML
- Not available yet
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Use the official source while a readable HTML version is being prepared.
Dates
- Published
- 2018
- Effective
- 2018
About this regulation
Medical Device Vigilance and Post-Market Surveillance
Post-market surveillance requirements including adverse event reporting, field safety corrective actions, and medical device advisories.
Vigilance Guidelines is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.