Subcommittee Subcommittee Title Published standards Standards under development
ISO/TC 276/SC 1 Analytical methods 13 9
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Standard and/or project under the direct responsibility of ISO/TC 276 Secretariat Stage ICS
Biotechnology — Data publication — Preliminary considerations and concepts
60.60
Biotechnology — Data interoperability for stem cell data — Part 1: Framework
60.60
Biotechnology — Data interoperability for stem cell data — Part 2: Key characteristics of stem cell data
40.60
Biotechnology — Data interoperability for stem cell data — Part 3: Schema of the database structure
20.00
Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
90.92
Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
20.00
Biotechnology — Predictive computational models in personalized medicine research — Part 2: Guidelines for implementing computational models in clinical integrated decision support systems
30.92
Biotechnology — Biobanking — Requirements for human neural stem cells derived from pluripotent stem cells
60.00
Biotechnology — Biobanking of parasites — Part 1: Helminths
60.60
Biotechnology — Biobanking — Requirements for human natural killer cells derived from pluripotent stem cells
30.60
Biotechnology — Biobanking — Requirements for sample containers for storing biological materials in biobanks
40.20
Biotechnology — Biobanking — Requirements for deep-sea biological materials
40.20
Biotechnology — Biobanking — General requirements for biobanking
90.92
Biotechnology — Biobanking — General requirements for biobanking
20.60
Biotechnology — Biobanking — Requirements for animal biological material
90.20
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 1: General requirements
95.99
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 2: Best practice guidance for ancillary material suppliers
95.99
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users
95.99
Biotechnology — Ancillary materials present during the production of cellular therapeutic products and gene therapy products
60.60
Biotechnology — Bioprocessing — General requirements for the design of packaging to contain cells for therapeutic use
60.60
Biotechnology — Requirements for data formatting and description in the life sciences
60.60
Biotechnology — Bioprocessing — General requirements for the bacteriophage preparation for therapeutic use
20.60
Biotechnology — Biobanking — Process and quality requirements for establishment, maintenance and characterization of mammalian cell lines
90.93
Biotechnology — Biobanking — Process and quality requirements for establishment, maintenance and characterization of mammalian cell lines — Amendment 1
60.60
Biotechnology — Specification on data management and publication in microbial resource centers
60.60
Biotechnology — Biobanking — General requirements for the validation and verification of processing methods for biological material in biobanks
60.60
Biotechnology — General requirements for transportation of cells for therapeutic use
60.60
Biotechnology — Biobanking — Implementation guide for ISO 20387
60.60
Biotechnology — Biobanking — Requirements for human mesenchymal stromal cells derived from umbilical cord tissue
60.60
Biotechnology — Biobanking — Requirements for the biobanking of plant biological material for research and development
90.20
Biotechnology — Provenance information model for biological material and data — Part 1: Design concepts and general requirements
20.00
Biotechnology — Provenance information model for biological material and data — Part 1: Design concepts and general requirements
90.92
Biotechnology — Provenance information model for biological material and data — Part 2: Common Provenance Model
20.00
Biotechnology — Provenance information model for biological material and data — Part 3: Provenance of Biological Material
20.00
Biotechnology — General requirements and considerations for cell line authentication
90.92
Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
20.00
Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
90.92
Biotechnology — General requirements for nucleic acid- and protein-based bio-devices
20.60
Biotechnology — Biobanking of microorganisms — Part 1: Bacteria and archaea
60.60
Biotechnology — Massively parallel DNA sequencing — General requirements for data processing of shotgun metagenomic sequences
60.60
Biotechnology — Validation of database used for nucleotide sequence evaluation
60.60
Biotechnology — Biobanking — Requirements for human and mouse pluripotent stem cells
60.60
Biotechnology — Biobanking — Requirements for human mesenchymal stromal cells derived from bone marrow
60.60
Biotechnology — Biobanking — General requirements for (semi-)automated storage and retrieval equipment
20.60
Biotechnology — Bioprocessing — General requirements for purification of extracellular vesicles
20.00

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