Фильтр :
Стандарт и/или проект находящийся в компетенции ISO/TC 276 Секретариата Этап ICS
Biotechnology — Data publication — Preliminary considerations and concepts
60.60
Biotechnology — Genome editing — Part 1: Vocabulary
60.60
Biotechnology — Genome editing — Part 1: Vocabulary — Amendment 1
60.60
Biotechnology — Data interoperability for stem cell data — Part 1: Framework
30.20
Biotechnology — General considerations and requirements for cell viability analytical methods — Part 1: Mammalian cells
20.00
Biotechnology — Recommendations and requirements for predictive computational models in personalized medicine research — Part 1: Guidelines for constructing, verifying and validating models
30.00
Biotechnology — Biobanking — Requirements for human neural stem cells derived from pluripotent stem cells
20.20
Biotechnology — Biobanking of parasites — Part 1: Helminths
20.20
Biotechnology — Biobanking — General requirements for biobanking
60.60
Biotechnology — Biobanking — Requirements for animal biological material
60.60
Biotechnology — Cell counting — Part 1: General guidance on cell counting methods
60.60
Biotechnology — Cell counting — Part 2: Experimental design and statistical analysis to quantify counting method performance
60.60
Biotechnology — Requirements for evaluating the performance of quantification methods for nucleic acid target sequences — qPCR and dPCR
60.60
Biotechnology — Massively parallel sequencing — Part 1: Nucleic acid and library preparation
60.60
Biotechnology — Massively parallel sequencing — Part 2: Quality evaluation of sequencing data
60.60
Biotechnology — Massively parallel sequencing — Part 3: General requirements and guidance for metagenomics
20.00
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
40.99
Biotechnology — Nucleic acid synthesis — Part 1: Requirements for the production and quality control of synthesized oligonucleotides
60.60
Biotechnology — Nucleic acid synthesis — Part 2: General definitions and requirements for the production and quality control of synthesized gene fragment, gene, and genome
30.60
Biotechnology — Requirements for data formatting and description in the life sciences
60.60
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 — Analytical methods — General requirements and considerations for the testing and characterization of cellular therapeutic products
60.60
Biotechnology — Biobanking — Requirements for the biobanking of plant biological material for research and development
60.60
Biotechnology — Provenance information model for biological material and data — Part 1: Design concepts and general requirements
30.20
Biotechnology — General requirements and considerations for cell line authentication
30.60
Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
60.60
Biotechnology — Biobanking of microorganisms — Part 1: Bacteria and archaea
60.60
Biotechnology — Analytical Methods — Risk-based approach for method selection and validation for rapid microbial detection in bioprocesses
40.60
Biotechnology — Massively parallel DNA sequencing — General requirements for data processing of shotgun metagenomics
30.60
Biotechnology — Minimum requirements for optical signal measurements in photometric methods for biological samples
40.60
Biotechnology — Minimum requirements for cellular morphological analysis — Image capture, image processing, and morphometry
30.00
Biotechnology — Validation of Database used for nucleotide sequence evaluation
30.00
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

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