IDMP Changes on your mind?
Pluaris™ to Automate IDMP Documents
A comprehensive IDMP software, backed by AI, which seamlessly brings in the necessary characteristics from various systems and databases to meet IDMP compliance.
Key Benefits of Pluaris
Remove manual data gathering, improve performance, and continually be compliant for IDMP standards.
What does Pluaris Solve?
No POC Needed
Value From Day One
Pluaris does not require a 3-4 month POC or project timeline. Our software connects to your existing systems, grabs the necessary information, and creates a report to submit for IDMP compliance. And Pluaris continuously updates its documentation as IDMP regulations evolve.
Standardize Product Information
Pluaris quickly and accurately extracts, standardizes, and structures thousands of data elements for each product.
Continued Compliance Checks
Pluaris continually checks IDMP regulations for new documentation requirements and standards.
Comprehensive Data Management
Pluaris pulls in information spread across various systems and databases to create IDMP compliance documents.
Ready to Use From Day One
What Data Is Gathered?
Data is broken up between Medicinal Products, Clinical Particulars, Pharma Particulars, Ingredients/Substances, Packaging and Manufacturing. There are approximately 250 data fields collected within those buckets, depending on your organization.
The amount of data required for IDMP quickly adds up when you consider its entire complex structure.
This information describes:
- What a product is
- Where it is authorized
- How it looks
- Where its ingredients and parts come from
Who Is Involved?
There must be an extremely high level of collaboration between departments to assure compliance.