All Stories

  1. Feedback from The EBF – Focus Workshop: Bringing Assay Validation and Analysis of Biomarkers Into Practice
  2. The application of capillary microsampling in GLP toxicology studies
  3. Biomarker assay validation: are we having the right discussions?
  4. Assessment of light stability of drugs in blood and plasma
  5. Co-medication and interference testing in bioanalysis: a European Bioanalysis Forum recommendation
  6. Best practices for metabolite quantification in drug development: updated recommendation from the European Bioanalysis Forum
  7. Microscale bioanalysis
  8. Bioanalysis of ibrutinib and its active metabolite in human plasma: selectivity issue, impact assessment and resolution
  9. Tiered approach into practice: scientific validation for chromatography-based assays in early development – a recommendation from the European Bioanalysis Forum
  10. Scientific or regulated validation: a tiered approach? Meeting report from a joint EBF/DVDMDG workshop
  11. Determination of tapentadol and tapentadol-O-glucuronide in human serum samples by UPLC–MS/MS
  12. Implementing Dried Blood Spot Sampling for Clinical Pharmacokinetic Determinations: Considerations from the IQ Consortium Microsampling Working Group
  13. Introduction to the Proposals from the Global Bioanalysis Consortium Harmonization Team
  14. EBF: reflection on bioanalytical assay requirements used to support liquid microsampling
  15. Feedback from the European Bioanalysis Forum Workshop: taking tiered approach to the next level
  16. European Bioanalysis Forum continued plans to support liquid microsampling
  17. Feedback from a European Bioanalysis Forum survey on bioanalysis of drugs in tissues
  18. Recommendations from the European Bioanalysis Forum on method establishment for tissue homogenates
  19. Tiered approach: from plan into practice
  20. Tiered approach revisited: introducing stage-appropriate or assay-appropriate scientific validation
  21. Bioanalysis for plasma protein binding studies in drug discovery and drug development: views and recommendations of the European Bioanalysis Forum
  22. Conference Report: AAPS and US FDA Crystal City V meeting on Quantitative Bioanalytical Method Validation and Implementation: feedback from the EBF
  23. New Frontiers—Accelerator Mass Spectrometry (AMS): Recommendation for Best Practices and Harmonization from Global Bioanalysis Consortium Harmonization Team
  24. In-depth study of homogeneity in DBS using two different techniques: results from the EBF DBS-microsampling consortium
  25. LC–MS/MS of large molecules in a regulated bioanalytical environment – which acceptance criteria to apply?
  26. The effect of hematocrit on bioanalysis of DBS: results from the EBF DBS-microsampling consortium
  27. IS addition in bioanalysis of DBS: results from the EBF DBS-microsampling consortium
  28. Update of the EBF recommendation for the use of DBS in regulated bioanalysis integrating the conclusions from the EBF DBS-microsampling consortium
  29. Current Regulations for Bioanalytical Method Validations
  30. The European Bioanalysis Forum community’s evaluation, interpretation and implementation of the European Medicines Agency guideline on Bioanalytical Method Validation
  31. Managing scientific, technical and regulatory innovation in regulated bioanalysis: a discussion paper from the European Bioanalysis Forum
  32. Conference Report: The 3rd EBF Focus Meeting: ‘Hatching’ – emerging technologies approaching the regulated bioanalysis laboratory
  33. European Bioanalysis Forum recommendation: scientific validation of quantification by accelerator mass spectrometry
  34. European Bioanalysis Forum recommendation on method establishment and bioanalysis of biomarkers in support of drug development
  35. Updates from the EBF DBS–microsampling consortium
  36. Conference Report: ‘Less is More’: defining modern bioanalysis
  37. Conference Report: ‘Large Meets Small’: connecting the bioanalytical community around peptide and protein bioanalysis with LC–MS(/MS)
  38. Anticoagulant counter ion impact on bioanalytical LC–MS/MS assay performance: additional validation required?
  39. Anticoagulant counter ion impact on bioanalytical LC–MS/MS assays: results from discussions and experiments within the European Bioanalysis Forum
  40. EBF and dried blood spots: from recommendations to potential resolution
  41. EBF recommendation on the validation of bioanalytical methods for dried blood spots
  42. Blood stability testing: European Bioanalysis Forum view on current challenges for regulated bioanalysis
  43. Conference Report: From challenges to solutions
  44. A screening UHPLC–MS/MS method for the analysis of amyloid peptides in cerebrospinal fluid of preclinical species
  45. Conference Report: Connecting strategies on dried blood spots
  46. Building the Global Bioanalysis Consortium – working towards a functional globally acceptable and harmonized guideline on bioanalytical method validation
  47. Best practices in a tiered approach to metabolite quantification: views and recommendations of the European Bioanalysis Forum
  48. Towards harmonized regulations for bioanalysis: moving forward!
  49. Request for Global Harmonization of the Guidance for Bioanalytical Method Validation and Sample Analysis
  50. Incurred sample reproducibility: views and recommendations by the European Bioanalysis Forum
  51. European Bioanalysis Forum and the way forward towards harmonized regulations
  52. Darunavir Concentrations in Cerebrospinal Fluid and Blood in HIV-1–Infected Individuals
  53. Which Human Metabolites Have We MIST? Retrospective Analysis, Practical Aspects, and Perspectives For Metabolite Identification and Quantification in Pharmaceutical Development
  54. Validated LC–MS/MS methods for the determination of risperidone and the enantiomers of 9-hydroxyrisperidone in human plasma and urine
  55. Selection of a Respiratory Syncytial Virus Fusion Inhibitor Clinical Candidate, Part 1:  Improving the Pharmacokinetic Profile Using the Structure−Property Relationship
  56. Population pharmacokinetic model of fluvoxamine in rats: Utility for application in animal behavioral studies
  57. New model for intravenous drug administration and blood sampling in the awake rat, designed to increase quality and throughput for in vivo pharmacokinetic analysis
  58. Synthesis of Novel Diarylpyrimidine Analogues and Their Antiviral Activity against Human Immunodeficiency Virus Type 1
  59. Self-assembling PEG-p(CL-co-TMC) copolymers for oral delivery of poorly water-soluble drugs: a case study with risperidone
  60. Short duration aerosols of JNJ 2408068 (R170591) administered prophylactically or therapeutically protect cotton rats from experimental respiratory syncytial virus infection
  61. Assay Methods for Sufentanil in Plasma
  62. Deuterated Ritanserin analysis by gas chromatography/mass spectrometry: A sensitive technique to study human Ritanserin pharmacokinetics
  63. The Use of Stable-Isotope Methodology in Pharmacokinetic Studies Involving Flunarizine
  64. Reliability of Sufentanil Plasma Level Assays in Patients