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  • Solutions
    • Overview
    • Phase II - III Clinical Trials
    • Clinical Data Management
    • Oncology Clinical Trials
    • Investigator-Driven Clinical Trials
    • Proof-of-Concept Phase II Trials
    • IND Drug Safety Solutions
    • for Startups / Biotechs
    • for Pharma
    • for Academic Groups
    • for CROs
  • Services
    • Overview
    • Consulting - Clinical Trial Designs
    • CRF Design
    • Routine Data Management
    • Medical Review
    • Central Data Monitoring
    • Data Coding
    • SAE Reconciliation
    • Data Imports - Exports
    • DSMBs
    • SAE Management
    • Biostatistics
    • Reporting - CSRs
  • Products
    • Overview
    • EDCpro - Clinical Data Management Software
      • EDCpro - Overview
      • CRF Libraries and Protocol Guided Data Entry™
      • EDCpro: Randomization - IWRS
      • EDCpro: Study Drug Supply Management
      • EDCpro: Protocol Amendments
      • EDCpro: Data Imports
      • EDCpro: Data Management
      • EDCpro: Data Exports
    • SAEpro - IND Drug Safety System
    • CDMmanager: Paper-based Data Management System
    • e-Clinical Solutions for IND Stage Trials
  • Compliance
    • Data Standards
    • Quality Policy Quality Assurance
    • Compliance - IT Infrastructure
  • About Us
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  • News
    • SciAn News Publications
    • Press Releases
Latest News
November 02, 2011
Miklos Schulz, SciAn presents at “Lunch & Learn” seminar at Pennsylvania Discovery District
October 26, 2011
St. Clare Chung, SciAn presents at Outsourcing In Clinical Trials - CANADA, Toronto, Canada
October 24, 2011
SciAn Introduces a Ground-Breaking Cost Effective Technology for Managing Clinical Data in EDC Oncology Trials
April 05, 2011
SciAn to attend Bio 2011 International Convention in Washington, D.C.
January 28, 2011
SciAn’s SAEpro software assists biotechs to comply with safety reporting under the new IND Safety Reporting requirements.

Welcome

Indication-Targeted EDC for Phase II-III Trials

SCiAN - a science-technology based contract clinical research company - provides e-clinical and EDC / Clinical Data Management services and systems to the healthcare industry.

Our edc / e-clinical system has been developed and refined over 15 years to:

  • Meet the demands of IND phase II - III clinical trials in indication-specific trial settings; 
  • Meet the needs of Project Managers, Study Coordinators, and CRAs;
  • Ensure the availability of consistent, credible, analysis-ready results throughout the study.

With the emergence of Software as a Service (SaaS) technology, we now offer our e-clinical, clinical data management (EDCPRO), and SAE-management (SAEPRO) solutions to Sponsors and clinical CROs on a monthly subscription basis with 3 levels of support.  

We invite you to visit our site and discover how we can assist you in your next clinical trial by:

Delivering Consistent & Credible Results

Services

Experience. Responsive. Standards.

With a portfolio of over 650 clinical trials, SCiAN's dedicated team can step in and support all data management, drug safety, biostatistics and medical writing aspects of a study in most indications, including: oncology, autoimmune - inflammatory, cardiovascular, CNS - neurology - pain, dermatology, diabetes - metabolic, gastroenterology, infectious, and respiratory diseases.

  • Consulting, Study Design
  • CRF Design
  • Clincal Data Management
  • Medical Review
  • Central Data Monitoring
  • Data Coding
  • SAE Reconciliation
  • Data Import - Exports
  • DSMBs
  • SAE Management
  • Biostatistics
  • Reporting - CSRs

All SciAn personnel are trained in EDCPRO and SAEPRO making the transition seamless for your study.



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