news

Rovi’s injectables CDMO rebrands as Rois and acquires BMS facility

0
SHARES

Gains US-based operations with its new Phoenix, Arizona injectable drug product manufacturing and packaging site.

Closed up image of a doctor holding a prefilled syringe in a line up of similar syringes

Spanish specialty pharma company Rovi Pharma Industrial Services has doubled down on its contract development and manufacturing organisation (CDMO) arm after deciding last year not to sell it.

 

ACCESS your FREE COPY

 


This report addresses the key factors shaping pharmaceutical formulation, including regulation, QC and analysis.

Access the full report now to discover the techniques, tools and innovations that are transforming pharmaceutical formulation, and learn how to position your organisation for long-term success.

What you’ll discover:

  • Key trends shaping the pharmaceutical formulation sector
  • Innovations leading progress in pharmaceutical formulation and how senior professionals can harness their benefits
  • Considerations and best practices when utilising QbD during formulation of oral solid dosage forms
  • And more!

Don’t miss your chance to access this exclusive report ! Access now – it’s free

The Madrid-headquartered firm will rebrand Rovi CDMO as Rois and it has gained a US facility through the acquisition of a Phoenix, Arizona injectable drug product manufacturing and packaging site from Bristol Myers Squibb (BMS).

Javier López-Belmonte, Vice Chairman of the Board and Chief Financial Officer at Rovi, said: “This acquisition is a strategic step in building Rois as a global CDMO for high-value injectables.

“The Phoenix site adds significant sterile fill-finish and high-potent capability, enabling us to better serve partners on US soil while continuing to invest across our network.”

The addition of direct US-based production capabilities comes amid sustained pressure from the US government for pharma companies to onshore their domestic production, with support for new-build pharma manufacturing facilities alongside tariff threats.

Rovi’s new Phoenix facility for its CDMO Rois occupies approximately 34,000 m² ofa site of around 80,000 m² that includes a cytotoxic/high-potent (OEB5) area and holds regulatory approvals from FDA, EMA and Japanese regulatory authorities. The US facility is also equipped for commercial-scale sterile fill-finish and packaging across vials, pre-filled syringes (PFS) and cartridges.

Over the next two years Rois plans to install an Optima PFS isolator line that is expected to add an annual PFS capacity of 65–70 million once it’s operational.

Before unveiling its new brand, Rovi had been considering a sale of its CDMO unit but decided not to last year despite receiving five offers for the business. Instead, Rovi will look to establish Rois as a global CDMO.

López-Belmonte added: “Our transformation into Rois reflects where we are today and where we are headed. We are proud of our legacy and excited about our future – growing, investing and expanding capacity to meet our partners’ needs worldwide.”

Share via
Share via