End-of-Phase 2AMeetings(EoP2)Confidentialityagreement(CDA)efficacyQualityAssuranceDeviationBiologicsLicenseApplication(BLA)ActivePharmaceuticalIngredient (API)EndpointPotencyInvestigationalNew DrugApplication(IND)21 CFRPart 210SpecificityPurityDrugproductexvivoInternationalConferenceonHarmonization(ICH)pharmacodynamicsChemistryManufacturingControls(CMC)CarcinogenicityNewChemicalEntity(NCE)FunctionalityBatchRecordsDrugMasterFile(DMF)FDAExpeditedPrograms orFast-TrackreviewCenter forBiologicsEvaluationand Research(CBER)OncologicDrugsAdvisoryCommittee(ODAC)Pre-ClinicalISO8Identity505(b)(1)vs.505(b)(2)QualityControlOrphandrugdesignation(ODD)BioequivalenceTeratogenicityAllogeneicCRISPRAdverseeventImmunogenicNon-disclosureagreement(NDA)INitial TargetedEngagement forRegulatoryAdvice CBERproducTs(INTERACT)BioavailabilityPhase321 CFRPart 11Phase1US Food andDrugAdministration(USFD/FDA)Phase2singleascendingdoseDrugsubstanceSterilityToxicityCertificateofAnalysisOut ofSpec(OOS)pharmacokineticsSafetyOpen-labelbenefit-riskprofilePre-NDA21 CFRPart 312StabilityAbbreviatedNew DrugApplication(ANDA)PharmacologyinvivoProof-of-ConceptCriticalrawmaterialEuropeanMedicinsAgency(EMA)ISO5ISO9001Free!Center forDrugEvaluationand Research(CDER)Pre-INDISO7BatchrecordsEnd-of-Phase 2AMeetings(EoP2)Confidentialityagreement(CDA)efficacyQualityAssuranceDeviationBiologicsLicenseApplication(BLA)ActivePharmaceuticalIngredient (API)EndpointPotencyInvestigationalNew DrugApplication(IND)21 CFRPart 210SpecificityPurityDrugproductexvivoInternationalConferenceonHarmonization(ICH)pharmacodynamicsChemistryManufacturingControls(CMC)CarcinogenicityNewChemicalEntity(NCE)FunctionalityBatchRecordsDrugMasterFile(DMF)FDAExpeditedPrograms orFast-TrackreviewCenter forBiologicsEvaluationand Research(CBER)OncologicDrugsAdvisoryCommittee(ODAC)Pre-ClinicalISO8Identity505(b)(1)vs.505(b)(2)QualityControlOrphandrugdesignation(ODD)BioequivalenceTeratogenicityAllogeneicCRISPRAdverseeventImmunogenicNon-disclosureagreement(NDA)INitial TargetedEngagement forRegulatoryAdvice CBERproducTs(INTERACT)BioavailabilityPhase321 CFRPart 11Phase1US Food andDrugAdministration(USFD/FDA)Phase2singleascendingdoseDrugsubstanceSterilityToxicityCertificateofAnalysisOut ofSpec(OOS)pharmacokineticsSafetyOpen-labelbenefit-riskprofilePre-NDA21 CFRPart 312StabilityAbbreviatedNew DrugApplication(ANDA)PharmacologyinvivoProof-of-ConceptCriticalrawmaterialEuropeanMedicinsAgency(EMA)ISO5ISO9001Free!Center forDrugEvaluationand Research(CDER)Pre-INDISO7Batchrecords

Untitled Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. End-of-Phase 2A Meetings (EoP2)
  2. Confidentiality agreement (CDA)
  3. efficacy
  4. Quality Assurance
  5. Deviation
  6. Biologics License Application (BLA)
  7. Active Pharmaceutical Ingredient (API)
  8. Endpoint
  9. Potency
  10. Investigational New Drug Application (IND)
  11. 21 CFR Part 210
  12. Specificity
  13. Purity
  14. Drug product
  15. ex vivo
  16. International Conference on Harmonization (ICH)
  17. pharmacodynamics
  18. Chemistry Manufacturing Controls (CMC)
  19. Carcinogenicity
  20. New Chemical Entity (NCE)
  21. Functionality
  22. Batch Records
  23. Drug Master File (DMF)
  24. FDA Expedited Programs or Fast-Track review
  25. Center for Biologics Evaluation and Research (CBER)
  26. Oncologic Drugs Advisory Committee (ODAC)
  27. Pre-Clinical
  28. ISO 8
  29. Identity
  30. 505(b)(1) vs. 505(b)(2)
  31. Quality Control
  32. Orphan drug designation (ODD)
  33. Bioequivalence
  34. Teratogenicity
  35. Allogeneic
  36. CRISPR
  37. Adverse event
  38. Immunogenic
  39. Non-disclosure agreement (NDA)
  40. INitial Targeted Engagement for Regulatory Advice CBER producTs (INTERACT)
  41. Bioavailability
  42. Phase 3
  43. 21 CFR Part 11
  44. Phase 1
  45. US Food and Drug Administration (USFD/FDA)
  46. Phase 2
  47. single ascending dose
  48. Drug substance
  49. Sterility
  50. Toxicity
  51. Certificate of Analysis
  52. Out of Spec (OOS)
  53. pharmacokinetics
  54. Safety
  55. Open-label
  56. benefit-risk profile
  57. Pre-NDA
  58. 21 CFR Part 312
  59. Stability
  60. Abbreviated New Drug Application (ANDA)
  61. Pharmacology
  62. in vivo
  63. Proof-of-Concept
  64. Critical raw material
  65. European Medicins Agency (EMA)
  66. ISO 5
  67. ISO 9001
  68. Free!
  69. Center for Drug Evaluation and Research (CDER)
  70. Pre-IND
  71. ISO 7
  72. Batch records