White Papers in Bioanalysis from Previous WRIB

• 2021 White Paper in Bioanalysis 
  was based on the conclusions and consensus points from the 15th WRIB in September 2021. It was divided into 3 parts due to length, and was just published on the Bioanalysis Journal (Future Science, UK).

  • Part 1A – Mass Spec of Proteins, Extracellular Vesicles, CRISPR, Chiral Assays, Oligos; Nanomedicines Bioanalysis; ICH M10 Section 7.1; Non-Liquid & Rare Matrices
    Part 1B – Regulatory Inputs
    • Recommendations on Endogenous Compounds, Small Molecules, Complex Methods, Regulated Mass Spec of Large Molecules, Small Molecule, PoC
    • Regulatory Agencies’ Inputs on Bioanalysis, Biomarkers, Immunogenicity, Gene & Cell Therapy and Vaccine
  • Part 2 – ISR for Biomarkers, Liquid Biopsies, Spectral Cytometry, Inhalation/Oral & Multispecific Biotherapeutics, Accuracy/LLOQ for Flow Cytometry
    • Recommendations on Biomarkers/CDx Assays Development & Validation, Cytometry Validation & Innovation, Biotherapeutics PK LBA Regulated Bioanalysis, Critical Reagents & Positive Controls Generation
  • Part 3 – TAb/NAb, Viral Vector CDx, Shedding Assays; CRISPR/Cas9 & CAR-T Immunogenicity; PCR & Vaccine Assay Performance; ADA Assay Comparability & Cut Point Appropriateness
    • Recommendations on Gene Therapy, Cell Therapy, Vaccine Assays; Immunogenicity of Biotherapeutics and Novel Modalities; Integrated Summary of Immunogenicity Harmonization

• WRIB Special Focus Issue on Critical Reagents

  • Current and effective strategies for critical reagent characterization, storage, stability, retesting and life cycle management for ligand-binding assays and flow cytometry”

• 2020 White Paper in Bioanalysis 
  was based on the conclusions and consensus points from the 14th WRIB in June 2020. It was divided into 3 parts due to length, and was published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – BMV of Hybrid Assays, Acoustic MS, HRMS, Data Integrity, Endogenous Compounds, Microsampling and Microbiome
    • Recommendations on Industry/Regulators Consensus on BMV of Biotherapeutics by LCMS, Advanced Application in Hybrid Assays, Regulatory Challenges in Mass Spec, Innovation in Small Molecules, Peptides and Oligos
  • Part 2A – BAV Guidance, CLSI H62, Biotherapeutics Stability, Parallelism Testing, CyTOF
    Part 2B – Regulatory Feedback
    • Recommendations on Biotherapeutics Stability, PK LBA Regulated Bioanalysis, Biomarkers Assays, Cytometry Validation & Innovation
    • Regulatory Agencies’ Inputs on Bioanalysis, Biomarkers, Immunogenicity, Gene & Cell Therapy and Vaccine
  • Part 3 – Vaccine Assay Validation, qPCR Assay Validation, QC for CAR-T Flow Cytometry, NAb Assay Harmonization and ELISpot Validation
    • Recommendations on Immunogenicity Assay Strategies, NAb Assays, Biosimilars and FDA/EMA Immunogenicity Guidance/Guideline, Gene & Cell Therapy and Vaccine Assays

• 2019 White Paper in Bioanalysis, Biomarkers, Immunogenicity and Gene Therapy 
  was based on the conclusions and consensus points from the 13th WRIB in April 2019. It was divided into 3 parts due to length, and was just published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – Chromatographic Assays - Innovation in Small Molecules and Oligonucleotides & Mass Spectrometric Method Development Strategies for Large Molecule Bioanalysis
  • Part 2 – FDA BMV Guidance, ICH M10 BMV Guideline and Regulatory Inputs - Recommendations on 2018 FDA BMV Guidance, 2019 ICH M10 BMV Draft Guideline and Regulatory Agencies’ Input on Bioanalysis, Biomarkers and Immunogenicity
  • Part 3 – FDA Immunogenicity Guidance, Gene Therapy, Critical Reagents, Biomarkers and Flow Cytometry Validation - Recommendations on 2019 FDA Immunogenicity Guidance, Gene Therapy Bioanalytical Challenges, Strategies for Critical Reagent Management, Biomarker Assay Validation, Flow Cytometry Validation & CLSI H62

• 2018 White Paper in Bioanalysis, Biomarkers, Immunogenicity and Gene Therapy 
  was based on the conclusions and consensus points from the 12th WRIB in April 2018. It was divided into 3 parts due to length, and was published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – small molecule regulated bioanalysis, small molecule biomarkers, peptides & oligonucleotide bioanalysis - A global bioanalytical community perspective on last decade of incurred samples reanalysis (ISR)
  • Part 2 – PK, PD & ADA assays by hybrid LBA/LCMS & regulatory agencies’ inputs on bioanalysis, biomarkers and immunogenicity - focus on immunogenicity assays by hybrid LBA/LCMS and regulatory feedback
  • Part 3 – LBA/cell-based assays: immunogenicity, biomarkers and PK assays - focus on flow cytometry, gene therapy, cut points and key clarifications on BAV

• 2017 White Paper in Bioanalysis, Biomarkers and Immunogenicity 
  was based on the conclusions and consensus points from the 11th WRIB in April 2017. It was divided into 3 parts due to length, and was just published on the Bioanalysis Journal (Future Science, UK).

  • Part 1: SM, Peptides and SM Biomarkers by LCMS - Aren’t BMV Guidance “Scientific”
  • Part 2: Hybrid LBA/LCMS and Inputs from Regulatory Agencies - Rise of the Hybrid LBA/LCMS Immunogenicity Assays
  • Part 3: Immunogenicity, Biomarkers and PK Assays - A Global Perspective on Immunogenicity Guidelines & Biomarker Assays Performance

• Decennial Index of all the recommendations from 2007 to 2016's WRIB White Papers to help you search easily by topics and see the evolution of the recommendations on the same topic over the years.

  • The Decennial Index of the White Papers in Bioanalysis: “A Decade of Recommendations (2007–2016)”
    Note: you must save the pdf file to your computer then re-open it from your computer in order to activate the search functions in the pdf.

• 2016 White Paper in Bioanalysis: Focus on Biomarker Assay Validation (BAV) 
  was based on the conclusions and consensus points from the 10th WRIB in April 2016. It was divided into 3 parts due to length, and was published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – Small Molecules, Peptides and Small Molecule Biomarkers by LCMS
  • Part 2 – Hybrid LBA/LCMS and Inputs from Regulatory Agencies
  • Part 3 – LBA, Biomarkers, and Immunogenicity

• 2015 White Paper in Bioanalysis: Focus on New Technologies and Biomarkers 
  was based on the conclusions and consensus points from the 9th WRIB in April 2015. It was divided into 3 parts due to length, and was published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – Small Molecules by LCMS
  • Part 2 – Hybrid LBA/LCMS and Inputs from Regulatory Agencies
  • Part 3 – LBA, Biomarkers, and Immunogenicity

• 2014 White Paper on Recent Issues in Bioanalysis: A Full Immersion in Bioanalysis 
  was based on the conclusions and consensus points from the 8th WRIB in March 2014. It was divided into 3 parts due to length, and was published on the Bioanalysis Journal (Future Science, UK).

  • Part 1 – Small Molecules by LCMS
  • Part 2 – Hybrid LBA/LCMS, ELN and Regulatory Agencies' Input
  • Part 3 – LBA & Immunogenicity

• 2013 White Paper on Recent Issues in Bioanalysis: "Hybrid" - The Best of LBA & LCMS 
  was based on the conclusions and consensus points from the 7th WRIB, and was published on the Bioanalysis Journal (Future Science, UK).

• 2012 White Paper on Recent Issues in Bioanalysis and Alignment of Multiple Guidelines 
  was based on the conclusions and consensus points from the 6th WRIB, and was published on the Bioanalysis Journal (Future Science, UK).

• 2011 White Paper on Recent Issues in Bioanalysis and Regulatory Findings from Audits and Inspections 
  was based on the conclusions and consensus points from the 5th WRIB, and was published on the Bioanalysis Journal (Future Science, UK).

• 2010 White Paper on Recent Issues in Regulated Bioanalysis & Global Harmonization of Bioanalytical Guidance 
  was based on the conclusions and consensus points from the 4th WRIB, and was published on the Bioanalysis Journal (Future Science, UK).

• 2009 White Paper on Recent Issues in Regulated Bioanalysis 
  was based on the conclusions and consensus points from the 3rd WRIB, and was published on the Bioanalysis Journal (Future Science, UK).

• 2008 White Paper was based on the conclusions and consensus points from the 2nd Workshop on Recent Issues in GLP Bioanalysis, and was published on the Bioanalysis Journal (Future Science, UK).