Pure Global AI
ABMed EC-FO-

EC-FO- 0001

Checklist des documents à soumettre pour une demande d’AEC
BeninAgence béninoise du Médicament et des autres produits de SantéClinical TrialsCurrentness under review
Official source linked
Document status

Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.

What this code is

EC-FO- 0001 is the official ABMed identifier for “Checklist des documents à soumettre pour une demande d’AEC”. EC-FO- 0001 is the official identifier ABMed uses for this instrument.

Instrument
EC-FO-
Full name
EC-FO- 0001
Category
Clinical Trials
Source links
Source publication
French
Open the source text
Linked source text; confirm the publisher, publication details and any later amendment or consolidated version.
Readable HTML
1 language version
Read the full text →
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
—
Effective
—
Readable full text

Open a language version

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

French full textFrench — original textRead HTML →
About this regulation

Checklist des documents à soumettre pour une demande d’AEC

Clinical-trial submission checklist. Device and IVD trials require general items 1–12 and 17–28 plus ten additional documents covering device design, risk assessment, biological safety, sterilisation and other supporting evidence.

EC-FO- 0001 is the official identifier ABMed uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

Source linked