Technology that makes the operation visible.
Pixoom digitizes regulatory management: processes, documents and indicators in one place, with automation in place of spreadsheets.
Fewer spreadsheets, more visible process.
Pixoom is the group's software house. It brings processes, documents and indicators into one platform, with automation in place of manual controls, so every regulatory step is recorded and visible.
Who it is for
Organizations regulated by the Brazilian Health Regulatory Agency (Anvisa) and other oversight bodies, in these segments:
- Medicines
- Medical devices
- Cosmetics
- Sanitizers
- Food
- Other regulated products
The history of each process, in one place.
Medical device registration calls for a form, a technical dossier and, for imports, specific documents. Scattered across spreadsheets, folders and emails, they are hard to follow. At Pixoom, each document, action and delivery is recorded in a single history.
Form
- Scattered
- Spreadsheet
- In a single history
- Recorded
Technical dossier
- Scattered
- Folder
- In a single history
- Recorded
Import documents
- Scattered
- In a single history
- Recorded
How Pixoom works.
Diagnosis
We identify bottlenecks and inefficient flows, with interactive mapping and data analysis.
Modeling and automation
We design custom flows and automate tasks, with less rework and more traceability.
Monitoring
Custom dashboards and alerts show what is happening as it happens.
Results
Every indicator, action and delivery is recorded, with regulatory business intelligence (BI) and auditable compliance.
Pixoom serves the whole group.
Receives from Ávita Care
Receives the strategy from Soluto Regulatórios and the registrations from Ávita Care: documents, steps and deadlines.
Technology & Automation
Hands over to Évira Pharma
Keeps the access journey of Évira Pharma visible in real time.
Which regulated sectors Pixoom works in: Regulated sectors
