Migrate critical business documentation securely and controlled
- Assessed project model based on current documentation standards
- Trained documentation specialists within ISO and GxP
- Practical and pragmatic consultancy services
Compliant documentation practice is vital to your business
But regulatory demands and often lacking document practices complicates your compliance processes around market entry, innovation, M&A, and project delivery.
You will lose opportunities
Administrative tasks take focus away from your actual, value-generating work.
You cannot go to market
Regulatory complexity puts your marketed products and business increasingly at risk.
You risk your reputation
Potentially ruining relationships and trust of stakeholders, public, and customers.
Get controlled data migration in full GxP
Avert regulatory backlash and get safely to market. We help your pharmaceutical business processes to ensure GxP in your clinical trials, mergers & acquisitions, and contractual agreements.
Migrate unstructured data in full GxP
Safely move critical documentation from legacy to modern enterprise document management systems without losing document integrity.
Import & classify eTMF in full control
Safely receive and consolidate Trial Master Files from external vendors. Mapped and ready for your internal systems and processes.
We got you covered
We carry your critical documentation tasks that you would rather not. We guide you through the critical phases with technological prowess and deep business accumen.
Free meeting, assessment & quote
Get a call and meeting. We help you identify where your project is and what you need to be aware of.
Structured plan & assistance
We help you control your document project and management, documented all throughout the project.
Business integrity maintained
Your documents and people connected to optimize your business processes and value.
