Staying on top of all developments with regard to ISO IDMP and associated requirements consumes precious resources. arivis subject matter experts follow the developments and translate them to a practical approach for pharmaceutical companies. Apart from the compliance requirements our staff understands IDMP as an opportunity for our clients to harmonize global data and processes, effectively gaining complete transparency in terms of product data compliance.
How we do it
Our IDMP approach is divided in phases that allow establishing continuous data compliance and processes for data maintenance at the same time.
- Quick Check
- Create Metrics
- Liaise with Management
- Decide Policy
- Build Execution Plan
Data Collection Phase
- Identification of relevant data sources
- Data (quality) assessment
- Establish Change Management Process
- Compilation, Extraction from source(s)
- Data Manipulation
- Import in platform & Maintenance