PRISYM Medica ClinTrial, our clinical trials solution, is an "add-on" software module to PRISYM Medica labelling software that provides additional features for clinical trials managing randomised labelling and records. PRISYM Medica ClinTrial is ideal for securely and accurately managing clinical trials data for supplies and complete patient kit / patient pack labelling.

PRISYM Medica ClinTrial software is a turn-key solution which will support you in passing audits required by the FDA.

PRISYM Medica ClinTrial can also help in meeting GMP GLP, GCP and ISO guidelines for clinical research trial samples, clinical trial phases and clinical trial drug labelling, drug packaging, and record keeping.

PRISYM Medica ClinTrial enables you to:

• Produce clinical trials phase label printing
• Secure access, event and audit logging
• Patient stratification
• Remove patients during a trial
• Manage multiple centre, visit and treatment logging
• Customise user-defined variables
• Randomisation based on treatments and stratification
• Randomise user definable group-weighting and sizing
• Import/export legacy databases (ODBC, DSN, CSV)
• Produce full product lifecycle documentation

Read more information about our Clinical trials labelling software

For pricing and other details please contact PRISYMID sales team. To understand more regarding our Life Sciences Solutions, please visit: www.prisymls.com