Pi reads the paste
It checks the supplied evidence against this form’s field descriptions.

Prepare the current ANVISA petition form used for Class III and IV medical device registration under RDC 751/2022 from company, manufacturer, site, classification, model, accessory, and responsible-person facts. Keep the regulator’s original editable file instead of receiving a generic AI report.
Use notes, an email, a product description, company details, or copied dossier content. The agent maps reliable facts into this form’s fixed JSON contract, then a deterministic writer fills the official DOCX template.
ANVISA currently lists this Word form for Class III and IV medical device registration petitions.
The agent can reason over unstructured notes without being trusted to modify the document package. The expected JSON is the handoff contract.
It checks the supplied evidence against this form’s field descriptions.
Every one of the 31 expected keys is present; missing evidence is null.
A deterministic adapter writes accepted values into fixed locations in the stored official template.
Turn pasted company and device facts into a review-ready draft of ANVISA’s official Ficha de Enquadramento V2 Word form.
Paste an unstructured portfolio or product list and download the official ANVISA model-list spreadsheet populated with extracted model names.
Paste applicant, establishment, device, and manufacturer facts and receive a preliminary filled copy of COFEPRIS’s FF-COFEPRIS-21 medical device registration and renewal Word form.
Use the same paste-first workflow to prepare editable cover letters, authorization or representation letters, powers of attorney, declarations, truthful statements, and Free Sale Certificate requests.
Open regulatory document buildersThis tool does not create an authority account, pay fees, sign, certify, or submit a filing. It transcribes the evidence you paste into the stored official template so your team can review and finish the draft.