RESEARCH Development Manufacture Distribution
ACTIVITY
  • Risk & safety assessment
  • Standard operating protocols
  • Commercial trials
  • Clinical trials
 
REQUIREMENT
  • Record; review, signature, filing, referencing
  • Material/sample identification/labeling
  • Material/sample tracking
  • Material/sample auditing
 
REGULATIONS
  • COSHH, D 91/356, CHIP3, GCP, GLP, GMP, GHS, 21 CFR Part 11, ISO


PRISYMLS COMPLIANT PRODUCT OFFERING:
 
PRISYM LAB PRISYM LAB/WEB PRISYM MEDICA
PRISYM MEDICA/WEB PRISYM CLINTRIAL PRISYM DEVICE
PRISYM SCL PRISYM CHEMICA  
 
See the reference, PR, links and glossary section of this page for more information and documentation on compliance requirements and regulations.