| Subcommittee | Subcommittee Title | Published standards | Standards under development |
|---|---|---|---|
| ISO/TC 276/SC 1 | Analytical methods | 13 | 9 |
Filter :
| 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 | |
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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
|
30.20 |
|
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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
|
60.60 | |
|
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 | |
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Biotechnology — Biobanking — Requirements for deep-sea biological materials
|
40.20 | |
|
Biotechnology — Biobanking — General requirements for biobanking
|
90.92 | |
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Biotechnology — Biobanking — General requirements for biobanking
|
30.20 |
|
|
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 | |
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Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users
|
95.99 | |
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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
|
30.20 |
|
|
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 | |
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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 | |
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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
|
30.00 |
|
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Biotechnology — Provenance information model for biological material and data — Part 1: Design concepts and general requirements
|
90.92 | |
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Biotechnology — Provenance information model for biological material and data — Part 2: Common Provenance Model
|
20.00 |
|
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Biotechnology — Provenance information model for biological material and data — Part 3: Provenance of Biological Material
|
20.00 |
|
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Biotechnology — General requirements and considerations for cell line authentication
|
90.92 | |
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Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
|
20.00 |
|
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Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
|
90.92 | |
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Biotechnology — General requirements for nucleic acid- and protein-based bio-devices
|
30.20 |
|
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Biotechnology — Biobanking of microorganisms — Part 1: Bacteria and archaea
|
60.60 | |
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Biotechnology — Massively parallel DNA sequencing — General requirements for data processing of shotgun metagenomic sequences
|
60.60 | |
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Biotechnology — Validation of database used for nucleotide sequence evaluation
|
60.60 | |
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Biotechnology — Biobanking — Requirements for human and mouse pluripotent stem cells
|
60.60 | |
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Biotechnology — Biobanking — Requirements for human mesenchymal stromal cells derived from bone marrow
|
60.60 | |
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Biotechnology — Biobanking — General requirements for (semi-)automated storage and retrieval equipment
|
20.60 |
|
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Biotechnology — Bioprocessing — General requirements for purification of extracellular vesicles
|
20.20 |
|
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