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Wrong Joris Bannenberg?

Joris Bannenberg

Chief Marketing Officer

Factory-CRO BV

HQ Phone:  +31 30 229 2727

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I agree to the Terms of Service and Privacy Policy. I understand that I will receive a subscription to ZoomInfo Community Edition at no charge in exchange for downloading and installing the ZoomInfo Contact Contributor utility which, among other features, involves sharing my business contacts as well as headers and signature blocks from emails that I receive.

Factory-CRO BV

Prof Bronkhorstlaan 10, Bld 54

Bilthoven, Utrecht,

Netherlands

Company Description

Factory-CRO is a leading, full service contract research organization focused on the management of clinical studies for medical devices, IVDs, biologicals, and device-drug combinations internationally. Founded in 1994, the business offers a full suite of trial... more

Find other employees at this company (30)

Background Information

Employment History

Manager Clinical Trials Medical Devices

Genzyme Corporation


Web References(12 Total References)


www.gclabsite.com

Clinical Device Group is proud to present Dr. Joris Bannenberg, medical doctor and Chief Operating Officer of Factory CRO, in the upcoming e-


www.kestercapital.com [cached]

Factory-CRO was founded over 20 years ago by Dr. Dirk Meijer and Dr. Joris Bannenberg.
Adam Maidment, founding partner at Kester Capital said, "Dirk and Joris have built an exceptional business in Factory-CRO and we are delighted to have the opportunity to partner with them to deliver the next phase of the business' growth. Dirk Meijer / Joris Bannenberg +31 30 229 2727


www.AmeriStart.com [cached]

- Joris Bannenberg, CEO, Factory CRO in Bilthoven, The Netherlands


www.AmeriStart.com [cached]

- Joris Bannenberg, CEO, Factory CRO,


www.mtbeurope.co.uk [cached]

This detailed information can save a manufacturer weeks or months of delay, and thousands of dollars of consultant fees," says Joris Bannenberg, COO of Factory Reimbursement.
The site contains detailed data aggregated from Austria, Belgium, Denmark, Finland, France, Germany, Italy, Norway, Poland, Spain, Sweden, Switzerland, The Czech Republic, The Netherlands, and The United Kingdom. "Quick access to this detailed regulatory data and reimbursement timelines will help any medical device manufacturer plan a more efficient entry into Europe," adds Bannenberg.


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