Expected field
Document date
Date displayed on the letter.
Free editable Word draft · No signup
Free Medical Device Letter of Authorization Builder
Create an editable preliminary medical device Letter of Authorization draft from manufacturer, authorized party, market, product, scope, duration, and signatory facts.
Paste facts in any format14 expected JSON fieldsEditable branded DOCXUnsupported facts stay blank
Paste the facts for this document
Formatting does not matter. Pi maps reliable facts into this document’s fixed JSON; deterministic code writes the branded editable Word file.
No signature, seal, notarization, legalization, or submission is applied.0 / 50,000
Document-specific contract
Facts this letter of authorization expects
Each field has its own description in the agent prompt and output schema. A key is always present in the JSON, but its value is null when the pasted material does not support it.
Expected field
Authorizing party legal name and address
Exact legal entity granting authority.
Expected field
Authorized party legal name and address
Exact authorized entity and identifiers.
Expected field
Territory and authority
Exact country/territory and regulator or purpose.
Expected field
Product and model scope
Only named products, models, accessories, and registrations.
Expected field
Authorized actions
Exact granted powers and responsibilities.
When applicable
Express limitations
Excluded powers, non-exclusivity, delegation limits, or other restrictions.
Expected field
Effective date
Effective date when supplied.
When applicable
Expiry and termination
Expiry date and termination mechanism when supplied.
Expected field
Signatory name
Name only; the generated file does not apply a signature.
Expected field
Signatory title
Job title or legal capacity.
Expected field
Signatory organization
Legal organization represented by the signatory.
When applicable
Signatory email
Contact email when supplied.
When applicable
Signatory telephone
Contact telephone when supplied.
Continue the regulatory workflow
Build a product master
Structure repeated company, product, model, approval, certificate, and evidence facts first.
Fill an official form
Use current stored ANVISA and COFEPRIS source artifacts with form-specific JSON.
Map dossier gaps
Turn an evidence index into a source-backed missing-attachment worklist.
Preflight the package
Check repeated facts, files, signatures, portal mapping, and release blockers.
Other regulatory document builders
Regulatory document builder FAQ
Does the AI write directly into an uncontrolled Word file?
No. Pi must first return the complete document-specific JSON contract. Deterministic code validates that object and writes the editable DOCX.
What happens when a required fact is not in my paste?
The field stays blank and appears in the review list. The workflow is instructed not to guess names, identifiers, dates, powers, classifications, standards, certificates, or authority language.
Does the tool sign, notarize, legalize, certify, or submit the document?
No. The output is an editable preliminary draft. Execution, acceptance, local wording, signatures, notarization, apostille, legalization, translation, and submission remain human responsibilities.
Can I edit the generated file?
Yes. The result is a native DOCX draft intended for review and editing in Microsoft Word or another compatible editor.