Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
|Articles|October 22, 2014

Roche to Expand and Improve its Basel Site

The renovation to Roche's historic office building in Basel, Switzerland will feature sustainable workplaces and a state-of-the-art research center.

Roche announced on Oct. 22, 2104 that it plans to expand its Basel office complex to “bring it into line with modern efficiency standards and building infrastructure requirements,” according to a press release from the company. The multibillion-dollar investment will help to upgrade existing infrastructure and will allow the site to satisfy standards for energy consumption, safety, and GMP.

“Roche is committed long-term to Switzerland and to Basel in its dual role as corporate headquarters and one of our most important sites worldwide . . . The new buildings will continue Roche’s tradition of elegant, distinctive, and functional architecture,” said Roche CEO Severin Schwan in a press release.

In addition to aesthetic changes, the makeover will include a new research center containing 950 offices and 950 laboratory workplaces, a new office building, and modern, low-rise buildings designed to encourage the use of public transportation and bicycles. The company is dedicated to sustainable design for the new construction project, which is projected to take 10 years to complete.

Source:
Roche

      


Related to this article

The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.
The BioPharm Brief: FDA Designations for a Bispecific CAR-T, a BLA for Friedreich’s Ataxia, and Phase 2b MASH Data for Efinopegdutide
FDA grants RMAT and Fast Track designations to AbelZeta’s CD20/CD19 bispecific CAR-T prizlon-cel in relapsed or refractory large B-cell lymphoma, Larimar Therapeutics completes a BLA seeking accelerated approval of nomlabofusp for Friedreich’s ataxia, and Merck’s GLP-1/glucagon receptor agonist efinopegdutide meets its primary endpoint in a phase 2b MASH trial.