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Solutions & Services

Technology Transfer

Our goal is continuous improvement of the quality of clinical data and optimization of processes for conducting clinical trials. Conduct your clinical research as efficiently and effectively as possible with our team and training.

  • Design and configuration of eCRFs (CDISC)
  • Specification and configuration of automatic checks
  • Dynamic logic for filling eCRFs
  • Validation of clinical trial data
  • Import of data from central laboratories, questionnaires, PK data, etc.
  • Data reconciliation in the EDC system with external sources
  • Generation of queries in the EDC system
  • Preparation of the database for interim and final analysis
  • AI Medical coding
  • Data processing for AEs and SAEs
  • Database lock
  • SAS datasets
  • Data export in any format
  • CDISC standards: CDASH, SDTM, Define.xml.
  • SCDM standards: GCDMP (Good Clinical Data Management Practice)

Advantages

Transparency at every step of working on the project
Quick project launch & speedy adjustments following protocol amendments
Consistent technology and know-how transfer
Validation effort optimization
Ongoing support and analytics
Best practices, useful techniques and knowledge sharing

Benefits from DM 365 Technology Transfer

  • Ensure smooth and deep dive
    into the system
  • Make use of generously shared useful techniques
    and data management best practices
  • Cut down costs and time when working on complex projects
  • Avoid redundancy and repetition of effort
  • Enjoy full tranparency of all processes on
    every step of the project

Pricing

Budget calculation of full Technology Transfer is based on the clinical trial design.
Having CDA mutually executed, please send your protocol/synopsis/assumptions to bd@datamanagement365.com and get your budget proposal.

Have you got any questions?

Contact us