Full forms List

Full Form List :

UDV Unit Dose Vial UKECA United Kingdom Ethics Committee Authority USP United States Pharmacopoeia WIPO World Intellectual Patent Office TGA Therapeutic Goods Administration, Australia TMF Trial Master File SARS Severe Acute Respiratory Syndrome SCDM Society for Clinical Data Management SIDS Sudden Infant Death Syndrome SIGAR Special Interest Group on Adverse Reactions R&D Research and Development RAPS Regulatory Affairs Professionals Society RCT Randomised Clinical Trials RDE Remote Data Entry RDS Research Defence Society REC Research Ethics Committee RGN Registered General Nurse RPSGB Royal Pharmaceutical Society of Great Britain RSM Royal Society of Medicine Rx Prescription QA Quality Assurance QSM-WHO Quality Assurance and Safety of Medicines (WHO) PDS Pharmacoepidemiology and Drug Safety (journal) PEM Prescription Event Monitoring PHRMA Pharmaceutical Research and Manufacturers Association PIL Package Insert Leaflet PMDA Pharmaceuticals and Medical Devices Agency, Japan PMS Post-Marketing Surveillance POM Prescription Only Medicine PSM Procurement and Supply Management PSUR Periodic Safety Update Report NAFDAC National Agency for Food and Drug Administration and Control, Nigeria NCPA National Community of Pharmacist Association NCPO National Conference of Pharmaceutical Organisations NDA New Drug Application NDMS National Disaster Medical System NME New Molecule Entity NSAID Non-Steroidal Anti-Inflammatory Drug IACUC Institutional Animal Care and Use Committee IAES Institutional Animal Ethics Committee ICDRA International Conference for Drug Regulatory Authorities ICH International Conference on Harmonization IIG Inactive Ingredient Guide  IMP Investigational Medicinal Products IMP - Investigational Medicinal Products IMPD Investigational Medicinal Product Dossier INDA Investigational New Drug Application INN International non-proprietary names (for pharmaceutical substances) INTDIS International Drug Information System - the previous WHO adverse reactions database IPC Indian Pharmaceutical Congress IPGA Indian Pharmacy Graduate Association ISO International Organization for Standardization ISoP International Society of Pharmacovigilance ISPE International Society for Pharmacoepidemiology HIS Indian Health Services  HPLC High Performance Liquid Chromatography HRSA Health Resources & Service Administration GCP Good Clinical Practices GLP Good Laboratory Practices GMP Good Manufacturing Practices FDA Food & Drug Administration FIP International Pharmaceutical Federations DRA Drug Regulatory Affairs DUMP Disposal of Unwanted Medicines and Poisons CADD Computer Aided Drug Design CDC Centre for Disease Control CIOMS Council for International Organisations of Medical Sciences CPCSEA Committee for Purpose of Control & Supervision of Experimental Animals CPI Consumer Price Index  CRA Clinical Research Associate CRC Clinical Research Council CRF Case Report Form CRN Clinical Research Network CRO Contract Research Organisation CSM Committee on Safety of Medicine CTC Clinical Trials Centre BMA British Medical Association BMJ British Medical Journal BPC Bulk Pharmaceutical Chemicals BPI British Pharmaceutical Index BrAPP British Association of Pharmaceutical Physicians AAAS American Association of Advancement of Science AALAS American Association for Laboratory Animal Science AIDS Acquired Immune Deficiency Syndrome  AIOPI Association of Information Officers of the Pharmaceutical Industry ALF American Liberation Front ANDA Abbreviated New Drug Application