Castor EDC of Amsterdam at MEDICA 2018 in Düsseldorf -- MEDICA - World Forum for Medicine

Castor EDC

Paasheuvelweg 25, Vleugel 5D, 1105 BP Amsterdam
Netherlands

This company is co-exhibitor of
Wearable Technologies AG

Hall map

MEDICA 2018 hall map (Hall 15): stand A23

Fairground map

MEDICA 2018 fairground map: Hall 15

Contact

Rob Konterman

COO

Phone
+31 20 337409

Email
sales@castoredc.com

Matthias Havenaar

BUSINESS DEVELOPMENT

Phone
+31 20 337409

Email
matthias.havenaar@castoredc.com

Ben Driesen

LEAD QUALITY ASSURANCE ENGINEER

Phone
+31 20 337409

Email
sales@castoredc.com

Bart Torentsma

INTERNATIONAL SALES & CLINICAL EPIDEMIOLOGIST

Phone
+31 20 337409

Email
sales@castoredc.com

Visit us

Hall 15 / A23

12.11.2018

Topic

all-day

Castor EDC Demo

Heading to MEDICA in Dusseldorf? Visit our booth in Hall 15, #A23. Learn how #CastorEDC can help you conduct faster, smarter medical #research.

Our team would be happy to chat with you about your clinical study requirements. Interested? Contact us to book a Castor EDC demo at our stand.

We look forward to seeing you there! #MEDICA2018

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Our range of products

Product categories

  • 06  Information and Communication Technology
  • 06.05  Administrative information systems / software
  • 06.05.01  Healthcare information systems / software (HIS)

Our products

Product category: Healthcare information systems / software (HIS)

Castor EDC - Electronic data capture solution

Castor is an Electronic Data Capture solution for medical device companies that offers a single platform for your design validation, clinical investigation and posts-market surveillance. Using Castor enables your company to save resources and become a frontrunner in MDR and GDPR compliance.

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Product category: Healthcare information systems / software (HIS)

MyConsent - Electronic patient consent platform

MyConsent is a an electronic patient consent platform that allows you to anonimously reach out to patients. By using secure authentication and cryptographic techniques, MyConsent facilitates the creation of an anonymous link between a research participant and datasets stored elsewhere. My consent allows companies / researchers to ask patients for consent for participation in clinical trials without having to know their identity. This way, research participants can remain anonymous while being in full control over the use of their data.

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Company news

Date

Topic

Download

Nov 1, 2018

Blog Article: In-vitro diagnostics regulation: From oversight to overhead

The rising demand for early, accurate disease diagnosis and the growing possibilities in personalised medicine are driving the demand for In-Vitro Diagnostic medical devices (IVDs). Thermometers, blood glucose monitoring devices and pregnancy tests, are an integral part of our lives.

Traditionally IVDs have been subject to little regulation when compared to medical devices or pharmaceuticals. The new In-Vitro Diagnostic Regulation (IVDR), however, will constitute a true quantum leap in regulatory burden. This white paper we will focus on the IVDR and how IVD companies can meet these regulatory changes. We will cover:

The regulatory framework
The new scope of IVDs
Changes in classification
New clinical evidence requirements

Download your copy of the White Paper from the link below

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Nov 1, 2018

Blog Article: What does the MDR tell us about post-market surveillance?

With the Medical Device Regulation (MDR) coming into full force in 2020, medical device companies should prepare for tougher Post-Market Surveillance (PMS) requirements. Companies will need to update their PMS procedures and should budget for more Post-Market Clinical Follow-up (PMCF) studies.

This article will address the role of Post-Market Surveillance during the lifecycle of your device, the specific requirements for Post-Market Surveillance under the MDR, and how an EDC system can help you fulfill these requirements in a cost-effective way. We will cover:

1) the role of Post-Market Surveillance during the lifecycle of your device;

2) the specific requirements for Post-Market Surveillance under the MDR;

3) how an Electronic Data Capture (EDC) system can help you fulfill these requirements in a cost-effective way.

Download your copy of the White Paper from the link below

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About us

Company details

Castor is an Electronic Data Capture solution that offers a single platform for your design validation, clinical investigation and posts-market surveillance. Using Castor enables your company to save resources and become a frontrunner in MDR and GDPR compliance.

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Company data

Sales volume

1-9 Mio US $

Number of employees

50-99

Area of business
  • Information and Communication Technology
  • Medical Services and Publications