Better Clinical Trial Execution Through eClinical Technology

Are You Ready for 2022?

Our experienced project management team and clinical monitors are trained to provide accurate, efficient, and on-time deliverables. We leverage industry-leading eClinical technology whenever possible to manage the trial, ensure participant safety, provide transparency, and proactively manage and mitigate risks. ICH-GCP and FDA mandate that Sponsors have meaningful oversight of their vendors and ensure subject safety and data integrity. DZS provides direct access to the experts you need to get it right.

Want insight into how we partner with organizations like yours on specific tasks?

 

 Our Whitepaper Is Out!

Click image to download

 

Business Matters

The Happy Secret to Better Work | Shawn Achor

 

Happy Thanksgiving!

Our team here at DZS wishes you a holiday filled with all the things that make you happiest, and the joy of being with those you love.

 

Connect With Us!

New to DZS?

Have you been looking for a full-service CRO providing clinical study support, data analytics solutions and pharmacovigilance capabilities to maximize efficiencies in your clinical trials?

If you are considering outsourcing these activities, connect with our team at www.dzs.com.

 

A Note From Our CEO

GREG AMBRA – CEO

At DZS, we are proud of our long history as a small, quality-focused service provider with a unique model to provide flexible client solutions through design and operational execution.

We believe true success is found in repeat clients. More than 90 percent of our sponsors execute multiple contracts with us, demonstrating our reputation for delivering exacting quality, our ability to meet aggressive timelines and our flexibility to customize solutions to meet specific needs. We’d love to know how we can support your team in the future!

Find out more about our services by contacting us directly at info@dzs.com!

 

DZS Clinical Services is a full-service CRO providing clinical study support, data analytics solutions and pharmacovigilance capabilities to maximize efficiencies in your global clinical trials.