How pharma can speed up digital transformation without risking quality or control?
Pharmaceutical manufacturers face a growing need to digitize operations yet paper-based processes and traditional validation methods continue to slow progress in regulated environments.
Composable low-code and no-code platforms offer a way forward, enabling rapid deployment and operational agility. Combined with Validation 4.0 principles, these solutions help organizations achieve both speed and compliance.
In this webinar, NNIT and Tulip will show how new technologies and modern validation strategies are transforming regulated manufacturing.
The webinar will cover:
- Revolutionizing Frontline Operations with Modern Solutions
- Platform-based solutions
- Enhancing composability in operations
- Embracing Validation 4.0
- Principles of Validation 4.0
- Transformative benefits and overcoming challenges
- Empowering Software Vendors
- How can software vendors support this journey
- Streamlining Regulated Customer Processes and Fast-Track Implementation with NNIT's Expert Services
- Efficient requirement gathering and system analysis
- Achieving compliance and speed in implementation
- Interactive Q&A Session
Speakers:
Michelle Vuolo, Head of Quality at Tulip
Nils Arne Jonescheit, Managing Consultant at NNIT
