Our products are scalable and flexible.

  • AIMDD: Active Implantable Medical Devices Directive
  • AITS:Adverse Incident Tracking System
  • ARM:Application to Reclassify a Medicine
  • BLA:Biological License Application
  • CA:Competent Authority
  • CAPLA:Computer Assisted Product Licence Application
  • CANDA:Computer Assisted New Drug Application
  • CD:Controlled Drug
  • CMS:Concerned Member State
  • CP:Centralised Procedure
  • CPP:Certificate of Pharmaceutical Product
  • CR:Computed radiology
  • CRO:Contract Research Organisation
  • CTA:Clinical Trial Application
  • CTC:Clinical Trials Certificate
  • CTD:Clinical Trials Directive
    Common Technical Document
  • CTX:Clinical Trials Exemption scheme
  • DB:Device Bulletin
  • DCP:Decentralised Procedure
  • DDX:Doctors and Dentist Exemptions
  • DIR:Diiagnostic Imaging Review
  • DMF:Drug Master File
  • DMRC:Digital radiology
  • DR:Device Bulletin
  • DB:Device Bulletin
  • DCP:Decentralised Procedure
  • DDX:Doctors and Dentist Exemptions
  • OTC:Over-The-Counter products
  • DIR:Diagnostic Imaging Review
  • DMF:Drug Master File
  • DMRC:Defective Medicines Report Centre
  • DR:Digital radiology
  • MDA:Medical Device Alert
  • MDD:Medical Devices Directive
  • MDR:Medical Device Reporting
    Medical Device Regulation
  • MDLO:Medical Device Liaison Officer
  • MEDDRA (MedDRA):Medical Dictionary for Drug Regulatory Affairs
  • ML:Manufacturer's Licence
  • MORE:Manufacturer's On-line Reporting Environment
  • ODD:Orphan Drug Designation
  • CT:Computed tomography