e-SOCDAT™ is an innovative, flexible, complete and interactive e-Clinical solution. It is a single web-based application uniting all core functional needs for the effective setup and conduct of a clinical research study.
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Socar Research SA
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Socar Research SA
Sophie De Brouwer
Chemin d●●●●●●●●merle 18
N●n , VD, 1260
CH
View this contact
Socar Research SA
Sophie De Brouwer
Chemin d●●●●●●●●merle 18
N●n , VD, 1260
CH
View this contact
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The Complete e-Clinical Solution | e-SOCDAT™ - SOCAR Research SA | esocdat.com Reviews
https://esocdat.com
e-SOCDAT™ is an innovative, flexible, complete and interactive e-Clinical solution. It is a single web-based application uniting all core functional needs for the effective setup and conduct of a clinical research study.
esocdat.com
Coordinating Centre's perspective | e-SOCDAT™ - SOCAR Research SA
http://www.esocdat.com/Advantages/CoordinatingCentre.aspx
SOCDAT™ from the Coordinating Centre's perspective. E-Clinical solution uniting interconnected components within a single application and database allowing the collection and management of clinical and operational metadata. Efficient study design using reliable, pre-validated data items. Electronic management and tracking of the Trial Master File documents, site visit contacts, source data verification and on-site visit reports. Adjustable system enabling targeted customisation.
electronic Data Capture | e-SOCDAT™ - SOCAR Research SA
http://www.esocdat.com/Features/e-DC.aspx
DC - electronic Data Capture. DC functionality is a straightforward, logical and user-friendly tool with role-based, user restricted access which allows site personnel (e.g. study nurses, investigators, pharmacists) to capture and access data for patients from their site. During the data management process, e-. For any new or updated serious adverse event, an automatic email notification can be sent to authorised safety personnel thereby guaranteeing the reporting of SAEs / SUSARs within required timelin...
Site Map | e-SOCDAT™ - SOCAR Research SA
http://www.esocdat.com/SiteMap.aspx
Website developed by SOCAR Research SA.
Sponsor's perspective | e-SOCDAT™ - SOCAR Research SA
http://www.esocdat.com/Advantages/Sponsor.aspx
SOCDAT™ from the sponsor's perspective. Fully validated, regulatory compliant and independently audited. Reduces time from study design to study reporting by optimising all project and data management steps. The e-. TMF enables a paperless management and tracking of the trial master file. Reduces (a) the need for face-to-face meetings, (b) manpower, (c) time and (d) paper generation and distribution. Flexible and compliant to any standard data format (e.g. CDISC, ODM).
Company | e-SOCDAT™ - SOCAR Research SA
http://www.esocdat.com/AboutUs/Company.aspx
Cachexia (chronic heart failure, oncology). Cerebrovascular, Central Nervous System. Haematology (iron deficiency anaemia). Metabolic (diabetes, lipidology). We provide exceptional personalised service to clients which, enhances the conduct and execution of high quality, scientifically-robust research studies in a flexible, time-efficient and cost-effective manner. Website developed by SOCAR Research SA.
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SOCAR Research SA | Services | Pharmacovigilance
http://www.socar-research.com/Services/Pharmacovigilance.aspx
We offer high responsive, customised pharmacovigilance services which are industry-standard compliant, ranging from small studies to complex, large multinational clinical studies and registries. Our pharmacovigilance services can be deployed individually or as a package. SOCAR offers the following pharmacovigilance services:. Design, development and implementation of the complete Adverse Event database. Data entry of adverse Events reports for trials using paper CRFs. Data query resolution and management.
SOCAR Research SA | Services | Regulatory Affairs
http://www.socar-research.com/Services/RegulatoryAffairs.aspx
At SOCAR, we understand the importance of submitting complete dossiers to the Competent Authorities and Ethics Committees. Submission of incomplete dossiers will lead to substantial delays in obtaining the final approvals which can not be recovered during the project life cycle. The regulatory services provided by SOCAR include:. Translation of documents as required. Application for EUdract number. Completion of CTA application. Collection and collation of all documents required for submission.
SOCAR Research SA | About Us | Values
http://www.socar.org/AboutUs/Values.aspx
Vision, Mission, Core Values. Our vision is to be an outstanding full-service clinical research organisation dedicated to good science, client satisfaction and industry-best solutions and innovation. We strive to deliver the most knowledgeable, timely, complete and responsive service possible. We aim to attract and retain talented and well-educated employees who serve our clients best interests working individually and as a team. We foster a collaborative and supportive work environment. We place the utm...
SOCAR Research SA | Communications
http://www.socar.org/Communications.aspx
Selected SOCAR publications and presentations. Selected list of publications:. 2011 Dec, 2(4):201-207. Epub 2011 Oct 16. Int J Cardiol. 161, 143 (2012). Circulation, 2011 May 3; 123 (17):1873-80. Zoltán Vokó, MD, PhD; Sophie de Brouwer, PhD; Jacobus Lubsen, MD, PhD; Nicolas Danchin, MD; Jan-Erik Otterstad, MD; Peter HJM Dunselman MD, PhD; Bridget-Anne Kirwan, PhD: Long-term impact of secondary preventive treatments in patients with stable angina. European Journal of Epidemiology: 02/2011;26 (5):375-83.
SOCAR Research SA | About Us | Careers
http://www.socar.org/AboutUs/Careers.aspx
SOCAR Research prides itself on hiring highly skilled and dedicated professionals. Our employees come from diverse backgrounds and generally fit one or more of the following profiles:. Have a record of excellence at a highly regarded college or university. Show advanced understanding in a relevant area of scientific expertise, mathematical modelling or statistics. Possess advanced skills in software programming, design, application or usage. Able and willing to work both independently and as a team member.
SOCAR Research SA | Services | Pharmacovigilance
http://www.socar.org/Services/Pharmacovigilance.aspx
We offer high responsive, customised pharmacovigilance services which are industry-standard compliant, ranging from small studies to complex, large multinational clinical studies and registries. Our pharmacovigilance services can be deployed individually or as a package. SOCAR offers the following pharmacovigilance services:. Design, development and implementation of the complete Adverse Event database. Data entry of adverse Events reports for trials using paper CRFs. Data query resolution and management.
Site Map | e-SOCDAT™ - SOCAR Research SA
http://www.socar.org/SiteMap.aspx
Website developed by SOCAR Research SA.
SOCAR Research SA | About Us | Industries Served
http://www.socar.org/AboutUs/IndustriesServed.aspx
SOCAR serves the following industries:. SOCAR can provide all of the resources needed to design, coordinate, manage, monitor and report on phase I to phase IV clinical trials and registries. Website developed by SOCAR Research SA.
SOCAR Research SA | About Us | Quality Management
http://www.socar.org/AboutUs/QualityManagement.aspx
SOCAR's approach to quality. SOCAR recognises that maintaining accuracy and quality is an essential continual, dynamic process in the lifecycle of a clinical research study. SOCAR's Quality Management System ensures reliability and accuracy of information in all steps of the clinical research projects carried out by us. SOCAR's Quality Management System may be summarised as follows:. SOCAR's approach to Quality. Sign off and approval of all study-related documents. Change control management procedures.
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The Complete e-Clinical Solution | e-SOCDAT™ - SOCAR Research SA
SOCDAT™ - The straightforward way to manage patient and operational metadata. SOCDAT™ is an innovative, flexible, complete and interactive e-Clinical solution. It is a single web-based application uniting all core functional needs for the effective setup and conduct of a clinical research study. This includes complete e-CRF design, electronic data capture, interactive web-based randomisation, electronic code break, complete data management, pharmacovigilance, electronic (a) endpoint adjud...
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