Case Report Form (CRF) Design & Clinical Coding
Case Report Form
The Case Report Form (CRF) is the central tool used in clinical trials. The CRF captures all the necessary data for each patient during a clinical trial. PAREXEL's experienced CRF design team understands that mistakes can cause expensive re-work and could compromise the validity of the data. We have the skill and knowledge to complete key set up task to the highest quality in order for your clinical trial to begin on a solid foundation.
Our CRF designers are located worldwide, these experts design CRFs and eCRFs for every phase of a clinical trial in numerous therapeutic areas. PAREXEL preserves a strong cross-functional relationship between the CRF design team, Clinical, Medical, Data Management, Clinical Programming and Biostatistics. This established relationship ensures database design, while ease of data entry and statistical output are equally considered during the creation of each CRF.
Data Services Printing Solutions
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Clinical Coding
PAREXEL’s extensive data management experience across a large number of therapeutic areas for many sponsors has directly resulted in the development of specialized global coding services. This provides our customers with a tailored and established service for your clinical coding needs.
Coding Related Services*
Stand-alone Coding: Provision of coding only services from within the WW Data Management organization. Coding can be performed through transfer of clinical trial datasets into PAREXEL systems or coding directly in the sponsors own environment.
Retrospective Coding: Re-coding of legacy Adverse Event data using specified versions of MedDRA. PAREXEL coding systems are utilized to standardize coding across desired projects / sponsor data.
Dictionary Upgrades: Analysis and upgrade of coded medical terminology to a required version of MedDRA or WHODRUG as appropriate.
*Subject to sponsor dictionary license status
Expert, Customized Training
Choose between customized or standard courses with high-level overviews and detailed technical information. We offer courses such as Introduction to MedRA, Advanced MedDRA and WHODRUG, which include hands on coding. We will work within your timelines, with convenient on-site training worldwide.
- Courses adapted to your system and organizational requirements
- Standard courses – provided per industry standards
- Sponsor defined timelines
- Efficient pricing – per class rather than per individual attendee
- Global coverage – to meet the needs of your global organization