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Research ArticleResearch

Roadmap to Implementation of a Rapid “Lab in a Pouch” NAT Method for Mycoplasma Testing

Philip Breugelmans, Karen De Roy, Orm Nieuwenhuizen and Heike Merget-Millitzer
PDA Journal of Pharmaceutical Science and Technology September 2025, 79 (5) 500-512; DOI: https://doi.org/10.5731/pdajpst.2024-003022.1
Philip Breugelmans
1Janssen Pharmaceutica NV, a Johnson & Johnson company, Turnhoutseweg 30, 2340 Beerse, Belgium;
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Karen De Roy
1Janssen Pharmaceutica NV, a Johnson & Johnson company, Turnhoutseweg 30, 2340 Beerse, Belgium;
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Orm Nieuwenhuizen
2Janssen Biologics B.V., a Johnson & Johnson Company, 2333 Leiden, The Netherlands; and
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Heike Merget-Millitzer
3Cilag GmbH International, a Johnson & Johnson Company, 8200 Schaffhausen, Switzerland
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  • For correspondence: hmergetm{at}its.jnj.com
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Abstract

Mycoplasma testing is a mandatory assay for all cell-derived products as part of the microbial control strategy. The compendial methods include an indicator cell culture method and a culture assay. Because the culture assay takes 28 days, the time-to-result (TTR) is one of the longest in the microbiology laboratory. Besides this, the compendial Mycoplasma methods are highly complex, subjective, and need strict segregation of labs to avoid cross-contamination with Mycoplasma. The pharmaceutical industry is seeking faster solutions, like nucleic acid testing (NAT)-based methods. There are alternative and rapid NAT methods on the market enabling a reduction of the TTR to approximately 1 day (1). Although some of these NAT methods offer partial automated solutions (e.g., nucleic acid extraction), many of them still require strict separation of test areas to avoid false-positive results and provide only limited hands-on-time reduction and simplification. In contrast, the BioFire® Filmarray® technology is a NAT method that is easy to use thanks to a closed process—a so called “lab in a pouch”—and provides the result within only 2 hours, including sample preparation. Besides the risk reduction of human errors due to the limited manual work involved, the automation can also lead to improved data integrity compared to the compendial method. This paper describes the roadmap of implementation of the BioFire® Filmarray® technology. The approach from feasibility studies to validation and regulatory submission for a monoclonal antibody (mAb)-based product is provided. As a first, J&J received regulatory approval from several agencies (including the US FDA and the EMA) to apply this technology for a biopharmaceutical product and has started global roll-out to additional products and testing sites. Understanding the risk concomitant with introducing new methods is essential to develop an appropriate validation, implementation, and filing strategy. The process applied at J&J for the first product will be shared in this publication.

  • Mycoplasma
  • Alternative and rapid microbiology method
  • PCR
  • Method validation
  • Comparability
  • Suitability testing
  • Simplification of microbiology testing
  • © PDA, Inc. 2025
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PDA Journal of Pharmaceutical Science and Technology: 79 (5)
PDA Journal of Pharmaceutical Science and Technology
Vol. 79, Issue 5
September/October 2025
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Roadmap to Implementation of a Rapid “Lab in a Pouch” NAT Method for Mycoplasma Testing
Philip Breugelmans, Karen De Roy, Orm Nieuwenhuizen, Heike Merget-Millitzer
PDA Journal of Pharmaceutical Science and Technology Sep 2025, 79 (5) 500-512; DOI: 10.5731/pdajpst.2024-003022.1

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Roadmap to Implementation of a Rapid “Lab in a Pouch” NAT Method for Mycoplasma Testing
Philip Breugelmans, Karen De Roy, Orm Nieuwenhuizen, Heike Merget-Millitzer
PDA Journal of Pharmaceutical Science and Technology Sep 2025, 79 (5) 500-512; DOI: 10.5731/pdajpst.2024-003022.1
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  • Article
    • Abstract
    • Introduction
    • Overview of the BioFire® Technology
    • Implementation Approach
    • Phase 1: Method Feasibility
    • Phase 2: Method Comparability
    • Phase 3: Generic GMP Method Validation
    • Phase 4: Suitability Testing
    • Phase 5: Filing and Regulatory Submission Approach
    • Phase 6: Implementation
    • Global Roll-Out of Method (Method Transfer)
    • Summary
    • Materials and Methods
    • BioFire® Mycoplasma PCR
    • Compendial Mycoplasma Assays
    • Conflict of Interest Declaration
    • Acknowledgments
    • References
  • Figures & Data
  • References
  • Info & Metrics
  • PDF

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Keywords

  • Mycoplasma
  • Alternative and rapid microbiology method
  • PCR
  • Method validation
  • Comparability
  • Suitability testing
  • Simplification of microbiology testing

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