For pharmaceutical and biotechnology managers seeking a production improvement partner that truly knows your business, RoviSys offers a full toolbox of proven automation resources, large-scale project management skills and a pragmatic get-it-done attitude. With RoviSys on your team, you can go confidently from requirements to post-implementation audit. We understand the philosophies and objectives behind your specifications and how the current project fits into your overall needs, current systems and potential opportunities. And we back it up with world-class automation and integration capability, extensive validation experience and the proven ability to implement and support our work.
As paper systems fall by the wayside, it is essential to have 21 CFR part 11 compliant automation and information systems that can keep you within the FDA requirements for reliable and secure records.
- Extensive project management experience from small to large scale projects
- Proven project execution methodology and a collaborative approach
- Dedicated experts capable of delivering solutions for your most challenging manufacturing applications
- Expertise of both modern and legacy automation and information systems
- Applications for your entire process:
- API Formulation
- Packaging & Inspection
- Control system architecture and design
- Life cycle documentation for GMP environments
- Validation services
- FEED studies
- Electrical and instrumentation design and installation
- Legacy migration
- MES design and implementation