Explore Biotech Products, Systems and Solutions
From concept through to design, biotech validation and production across all biotech applications, we can help you adapt to changing market conditions
with innovative technologies and solutions. Whether that means quickly developing a process for a new drug, vaccine production, helping you ensure regulatory compliance,
or making existing processes easier, faster and better, we are ready to work with you to address your process needs.
Overcome development and viral vector manufacturing obstacles to accelerate delivery of commercially viable gene therapies to patients.
Adeno-associated viruses (AAV) are small viruses that can infect humans and primates and can be found everywhere. In this blog, Dr Martin Glenz examines AAV in detail and explains why they lend themselves to gene therapy.
Join Dr Razan Jammal to discover a new level in filter integrity testing as we introduce our newest instrument and show you how it meets the latest industry needs and regulations to be first choice in critical applications.
Todd Lundeen and Andrew Laskowski take a detailed, technical look at how Aber’s FUTURA biomass proble provides reliable measurements when used with the iCELLis® nano bioreactor, correlating cumulative glucose consumption, nuclei counts, and capacitance.
More Posters and Presentations
Introducing the Palltronic® Flowstar V Filter Integrity Test Instrument
Watch our on-demand webinar to hear about our latest addition to the Palltronic family. Discover how you can get
- The highest assurance of data integrity and test accuracy
- Advanced automation options and faster network integration
- Improved quality risk management in your process
- All the benefits of our most intuitive and easy to use design yet
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Moving to integrated solutions will help simplify and streamline your manufacturing process, speeding time to market and reducing overall cost of goods. The simplified process using standard equipment, qualified designs and components lowers the risk for operator error, which helps assure compliance with cGMP and assure product quality. Our integrated solutions team combines best engineering and project management practices with in-depth industry knowledge and diverse equipment portfolio to deliver these benefits on time, and on budget.
Transparency and partnership are at our heart. We know the availability of high quality product documentation helps manage the documentation required for regulatory submission.
The Accelerator Documentation Center collates all current documentation to help you navigate compliance quickly and efficiently, and the electronic regulatory dossiers help you in your ongoing risk assessments to help alleviate the pressures of preparing documentation for regulatory compliance and audits.