# Epione EMR Template System v0.6 — Product / Device / Default Library

## Purpose

v0.6 adds a product and device default layer to the v0.5 clinical documentation framework.

This is **not** a formulary and not a claim that every named example is currently licensed or stocked. It is a structured verification and default-management library.

## Regulatory source logic

- Medications such as injectable corticosteroids, local anesthetics, contrast, ketamine, and injectable solutions should be checked in Health Canada's Drug Product Database (DPD): https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database.html
- Class II, III, and IV medical devices should be checked in MDALL: https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/licences/medical-devices-active-licence-listing.html
- MDALL API documentation for future automation: https://health-products.canada.ca/api/documentation/mdall-documentation-en.html
- PRP should be handled according to Health Canada's PRP clarification: https://recalls-rappels.canada.ca/en/alert-recall/health-canada-clarifies-position-platelet-rich-plasma-treatments
- Adult chronic pain nerve block image guidance/documentation should be checked against CPSO OHP requirements: https://www.cpso.on.ca/physicians/your-practice/accreditation-programs/out-of-hospital-premises-inspection-program/out-of-hospital-premises-standard-image-guidance-w

## Default hierarchy retained

Encounter input → per-form default → global default → blank for No Default fields.

## New sheets

1. Product_Dashboard
2. Product_Library
3. Product_Default_Profiles
4. Product_Field_Map
5. Verification_Workflow

## Practical use

1. Pick a product class in Product_Library.
2. Verify status in DPD/MDALL or supplier/MDEL pathway as applicable.
3. Record evidence in Verification_Workflow and your internal purchasing/QA records.
4. Only then set the product into Global_Defaults or Per_Form_Defaults.
5. Keep patient-specific items manual: laterality, diagnosis, lot/expiry, complications, actual volume, actual spread, dose/rate, image archive location, and procedure response.

## Current build counts

- Forms retained: 126
- Conditions retained: 36
- Product/device library rows: 32
- Product default profile rows: 20
- Product/device-related mapped fields: 473

