'Conducting a clinical trial resembles steering a car through a heavy traffic jam'.
Factory-CRO can help you navigate through this:
Regulatory insight. Our excellent relationship with competent authorities, ethic committees and other independent committees such as radiation committees has enabled us to help client start rapidly with their clinical trials in Europe.
Therapeutic area of expertise. For detailed information take a look at Expertise
Responsiveness and efficiency. Factory’s flat organization is a guarantee for low overhead costs, short and efficient communication lines. We work closely with the client’s staff and are very keen on the quality performance of clinical studies
Combined medical and technical knowledge. Our team consists of experienced medical device professionals each with medical, surgical or a research background. Surgical support during device implant procedures can be performed by our experienced staff. (See “People ” for profiles)
Adaptive data management service. Combined medical and technical knowledge. Our data-philisophy is that quality comes through speed and transparency.
Extensive network. Factory’s extensive network of contacts with surgeons of many different disciplines and Notified Bodies throughout Europe will help you to jump-start your clinical studies.
Broad operation field. With our multilingual staff in The Netherlands, our employees in France, Italy, Sweden, Hungary and the Netherlands Antilles; we cover the whole of Europe and more.
Excellent quality system. Factory is the first CRO in Europe to obtain ISO9001 certification for its Standard Operating Procedures. For more information take a look at Quality.
Access to specific patient populations. For example: On the Dutch Antilles we have access to a group of patients with Diabetics.
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