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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
    • Corporate Profile
    • Therapeutic Areas
    • Clients
  • News
    • SciAn News Publications
    • Press Releases
Latest News
May 16, 2012
Advanced EDC Trials - Webinar Session #1: The Unique Needs of Biotech/ Biopharma
March 12, 2012
SCiAN Services to Present at the Outsourcing in Clinical Trials Conference in Philadelphia, March 26, 20102: "Making EDC part of your quality control team through intelligent system implementation"
March 01, 2012
SCiAN Services to Present at the End-to-End Clinical Data Management Conference in Philadelphia, March 21, 2012: "Realizing the original promise of EDC: Achieving quality data on time in Phase II-III studies"
February 28, 2012
SCiAN Services Will be Exhibiting at Partnerships in Clinical Trials Conference in Orlando, Florida, March 4-7, 2012
November 02, 2011
Miklos Schulz, SciAn presents at “Lunch & Learn” seminar at Pennsylvania Discovery District

Welcome

Indication-Targeted EDC for Phase II-III Trials

SCiAN - a science-technology based Contract Research Organization - 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.

Services

Experience. Responsive. Standards.

With a portfolio of over 650 clinical trials, SCiAN's dedicated clinical data management and biostatistics 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
  • Clinical Data Management
  • Medical Monitoring - Review
  • Central Data Monitoring
  • Data Coding
  • SAE Reconciliation
  • Data Import - Exports
  • DSMBs
  • Pharmacovigilance - SAE Management
  • Biostatistics
  • Reporting - Safety Updates - CSRs

With 25 years experience as a North American Contract Research Organization:

Delivering Consistent & Credible Results



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