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