Your Trusted Global Partner
The future of pharma is here.
ALTEN Technology, at your service.
From lab to launch, we’ve got you covered.
Do you need help in CQV/CSV or Validating your Pharma production systems? ALTEN Technology can provide full services from design, install, launch, validation and verification from lab to launch.
When you partner with ALTEN Technology, you dramatically improve your Deviation Management controls on your production line. With a robust global network consisting of 3,000+ consultants and 53,000+ forward-thinking engineers, we can provide systemic processes for identifying, reporting, investigating, documenting, correcting, and preventing any departures from established standards in your pharmaceutical manufacturing process.
Let’s get to work.
ALTEN Technology can help with classification of deviations based on risk, root cause analysis, corrective and preventive actions (CAPA), and ensuring regulatory compliance through proper documentation and trending analysis. Our five main areas of expertise include:
- Automation
- Manufacturing — including Design & Installation
- Quality Assurance/Compliance/Deviation Management
- Validation/CQV/CSV/IT Solutions Powered by AI — including Commissioning, Qualification and Validation (CQV) and Computer System Validation (CSV)
- CRO full development cycle
Optimize how you produce products and protect patients with ALTEN Technology.
Case Studies
Here are a few examples of how we’ve served the world’s top pharma companies.
How We Partner
We partner with innovators in a variety of ways based on specific needs, including SOW-driven development; dedicated, flexible, and global teams; and on-site consulting. With offshore and nearshore resources necessary to control costs, our unmatched ability to accelerate ramp-up with a fully integrated team results in speed to market and product excellence. And with ALTEN Technology, you fully own all the IP we generate.