Smartlab Europe

ETH Zurich, CloudBroker select IBM Cloud Computing

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Roche AI Factory Expansion to Boost Pharma R&D Capacity

Swiss drugmaker Roche has expanded its artificial intelligence infrastructure...

It’s Time for the 3rd Generation of Patient Recruitment

Key Takeaways 80% of clinical trials experience enrolment delays and massive...

Driving Documentation Integrity Through Structured Drug Data

Establishing a robust framework for regulatory success requires moving beyond fragmented information silos toward a unified, digital-first approach. Comprehensive oversight of the pharmaceutical lifecycle depends on the ability to transform raw information into actionable insights, ensuring that every data point contributes to a larger narrative of safety and efficacy. By prioritizing specialized platforms that aggregate and organize complex information, organizations can achieve a level of transparency that satisfies the most stringent global standards while fostering a culture of continuous improvement.
- Advertisement -

ETH Zurich and CloudBroker, a provider of computing applications in the cloud, have selected IBM for cloud computing technology for conducting research to develop new antibiotics.
Under the agreement, the researchers of ETH Zurich’s Institute of Molecular Systems Biology will use IBM’s SmartCloud Enterprise and data management solutions of CloudBroker for identifying around 250 virulence factors or molecules that are secreted by bacteria, viruses, fungi, or protozoa and then multiply within humans.

Using IBM Smart Cloud Enterprise, the team of researchers had access to almost 250,000 computing hours on a total of 1,000 parallel CPU’s producing research on the structure of specific proteins found in the streptococcus bacteria which commonly causes strep throat in humans.

ETH Zurich lead researcher Lars Malmstrom said Cloud computing allows to reserve this computing capacity whenever researchers need it, and it is available quickly.”Research teams do not need to set it up or maintain it, and thus can concentrate better on their research,” Malmstrom said.

Latest stories

Related stories

Roche AI Factory Expansion to Boost Pharma R&D Capacity

Swiss drugmaker Roche has expanded its artificial intelligence infrastructure...

It’s Time for the 3rd Generation of Patient Recruitment

Key Takeaways 80% of clinical trials experience enrolment delays and massive...

Driving Documentation Integrity Through Structured Drug Data

Establishing a robust framework for regulatory success requires moving beyond fragmented information silos toward a unified, digital-first approach. Comprehensive oversight of the pharmaceutical lifecycle depends on the ability to transform raw information into actionable insights, ensuring that every data point contributes to a larger narrative of safety and efficacy. By prioritizing specialized platforms that aggregate and organize complex information, organizations can achieve a level of transparency that satisfies the most stringent global standards while fostering a culture of continuous improvement.

Contamination Control with Toxicological Reference Data

Centralizing expert-verified toxicological datasets is now a critical requirement for modern pharmaceutical facilities operating under stringent global regulations. By transitioning from generic cleaning limits to precise Health-Based Exposure Limits derived from high-quality platforms, manufacturers ensure that cleaning validation protocols are scientifically sound and audit-ready. This approach integrates rigorous toxicological risk assessment into the broader contamination control strategy, safeguarding patient health while optimizing multi-product manufacturing efficiency and regulatory compliance.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »