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Contacts: Anoto Partners within clinical trial solutions
Anoto licenses its de-facto standard digital pen & paper technology to a global network of partners. Our partners integrate our technology in their innovative, reliable solutions used in a growing number of industries. 

Below you find a list of partners working within the Clinical Trials area. Do not hesitate to contact them directly for any questions and requests.
 

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ExpeData, US
The EDW® digital writing platform solution powered by ExpeData automates the collection of handwritten information at the point of entry using multiple inputs including Anoto® digital pen and paper technology and the latest generation of tablet devices. Handwriting is captured in the field, immediately converted to digitized data and seamlessly integrated to backend business systems. This results in unsurpassed workflow optimization and significant cost reduction. For information visit www.expedata.net
Facts:
Number of pharma digital pens deployed: 1800
Number of countries of DPP Clinical Trial implementations: Over 25
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes

Case stories:
Accelerating information flow in clinical trials


Kayentis, FR
Kayentis is a leading integrator and operator of digital writing professional solutions specialized in Healthcare and Life Science, Manufacturing and Services sectors. Kayentis range of services improves key company process performance. Data collected by physicians, nurses, but also technicians and clerks in demanding environments such as healthcare, manufacturing or services are subject to strict levels of security and traceability. http://www.kayentis.com/

Facts:
Number of pharma digital pens deployed: 15.000
Number of countries of DPP Clinical Trial implementations: 50 over 5 continents
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes

Case stories:
Clinical trials worldwide aided by digital pen and paper
Digital pen and paper technology helps medical research centres in France

Video:
Make your CRF and Patient Diary Smart

Customer references:
Upon request
 
 

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Digital Field Solution, UK
We help businesses use mobile technology to make life easier and more productive for people in the field and on the move. For the pharmaceutical sector we have developed TRIALSCRIBE, a complete data capture solution for clinical trials.
http://www.digitalfieldsolutions.com/clinical/


Facts:

Number of pharma digital pens deployed: 100
Number of countries of DPP Clinical Trial implementations: 5
Audited by pharma companies: Yes
Certified CFR 21 part 11: No

 

 
Mi-Co, US
Mi-Co is the developer of Mi-Forms Digital Ink handwriting recognition and data cleaning technology and provides solutions for smart e-Forms data collection in a variety of industries including clinical research. Mi-Co’s enterprise Mi-Forms Software System enables flexible forms design and the capture, handwriting recognition, validation and automatic communication of forms-based data from handwritten source documents. Mi-Forms supports enterprise data capture using the Digital Pen & Paper technology, and has been validated for 21 CFR Part 11 compliance. Mi-Co’s Clinical Research customers include Sponsors, CROs and Clinical Sites that have seen up to 4x reductions in queries and 50% improvement in data-lock time using the technology. Mi-Co is headquartered in Durham, North Carolina. For more information on Mi-Co, please visit www.beyondedc.com

Facts:

Number of pharma digital pens deployed: 150
Number of countries of DPP Clinical Trial implementations: 5
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes

Case stories:
Providing fast and accurate data in Clinical Trials

White paper:
Beyond EDC: Resolving Data-entry Challenges faced by Electronic Data Capture Systems in Clinical Trials

Mi-Co in the media:
Pen-Based Site Visit Reporting Solution
SBIR Grant Award From the National Cancer Institute to Study Clinical Trials Data Collection
 
 

 
PharmaForms/Diagramm Hallbach, GE
Diagramm Halbach is an experienced service provider for digital pen and paper solutions. Being Anoto partner right from the beginning, we offer smart and complex solutions under the brand “dotforms® “. As we are certified print partner at the same time, dotforms® solutions are always harmonised regarding solution efficiency and paper functionality. http://www.pharmaforms.com/en/hn_3/hn_3_2.htm

Facts:

Number of pharma digital pens deployed: 800
Number of countries of DPP Clinical Trial implementations: 30
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes
 
 

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Arco Information, Belgium
Arco Information is a software editor and service provider specialized in document & workflow management, with a wide experience in Healthcare & Life Sciences (implementation of Phase I, II & III studies, patient diaries, healthcare /nursing records management for hospitals), as well as for the integration of  OCR (Optical Character Recognition) and digital pen technologies. A special emphasis is placed on flexibility (multimedia solutions, configurable workflows), performance, security and quality observance (21 CFR Part 11 compliance for the clinical area).
http://www.arco.be


GM Servizi, IT
ISO 27001 certified Service Provider focused and experienced in HealthCare and Facility Management sectors. Working with Anoto technology since 2003 we can supply our customer with full systems, consultancy, integration and validation services. Now dealing with many projects involving thousands of pens, patients and users (Clinical Trials / Reserarches). http://www.inkdata.eu/eng/default.htm

Facts:
Number of pharma digital pens deployed: 80-100
Number of countries of DPP Clinical Trial implementations: 1
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes

Case stories:
Clinical trials worldwide aided by digital pen and paper
Enabling broad epidemiological study 

Video:
Enabling broad epidemiological study

 

PopsiCube, FR
The next generation CRO, skilled in both IT and Clinical Research. We provide the best technology for data collection following your project specification under strict EU and FDA regulatory compliance.
Our offices based in Europe, North Africa and USA are cooperating with several CRO partners, which allows us to provide full CRO clinical services. http://www.popsicube.fr/

Facts:
Number of pharma digital pens deployed: 100+
Number of countries of DPP Clinical Trial implementations: 5
Audited by pharma companies: Yes
Certified CFR 21 part 11: Yes