ISO 20688, Biotechnology - Nucleic acid synthesis - General definitions and requirements for the production and quality control of synthetic nucleic acids
ISO 20397, Biotechnology - Methods to evaluate the quality of the massive sequencing data
ISO 20691, Biotechnology — Requirements for data formatting and description in the life sciences for downstream data processing and integration workflows
ISO 21710, Biotechnology - Specification on data management and publication in microbial resource centers
ISO 21709, Biotechnology - Biobanking - Process and quality requirements for establishment, maintenance and characterization of mammalian cell lines
ISO 23033, Biotechnology — Analytical methods — General guidelines for the characterization and testing of cellular therapeutic products
ISO/TS 20388, Biotechnology — Biobanking — Requirements for the collection, processing, storage and transportation of animal biological material
ISO/TS 23105, Biotechnology - Biobanking - Requirements for the collection, processing, transportation and storage of plant biological material
ISO 23118, Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
ISO 23162, Basic semen analysis - Specification and test methods
ISO/TS 22859, Biotechnology - Biobanking - Quality requirements for human mesenchymal stem cells
ISO 20166-4, Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: in situ detection techniques
ISO/TS 23565, Biotechnology - Bioprocessing - General requirements and considerations for equipment systems used in manufacturing of cellular therapeutic products
ISO 21474-2, In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Part 2 — Validation and Verification
ISO 20397-1, Biotechnology — General Requirements for Massive Parallel Sequencing — Part 1: Part 1: Nucleic acid and library preparation
ISO 24190, Biotechnology - General Requirements for Massive Parallel Sequencing - Part 1: Part 1: Nucleic acid and library preparation
EN ISO 17511, Medicintekniska produkter för in vitro-diagnostik - Krav för att fastställa metrologisk spårbarhet av värden som tilldelas kalibratorer, truenesskontrollmaterial och human prover
ISO 20184-3, Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNA
ISO 23511, Biotechnology — General requirements for cell line authentication
ISO 20397-2, Biotechnology - General requirements for massive parallel sequencing - Part 2: Methods to evaluate the quality of sequencing data
ISO 24088, Biotechnology - Collection, processing, storage and transportation requirements for microorganisms - part 1: Bacteria and archaea
ISO 24603, Biotechnology - Biobanking - The establishment, maintenance, characterization and distribution requirements for pluripotent stem cells
ISO 24651, Biotechnology - Biobanking - General requirements for biobanking of human mesenchymal stromal cells derived from bone marrow
EN ISO 20916, In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice
ISO 17593, In vitro diagnostik - Krav avseende självtestning vid peroral trombosförebyggande behandling
ISO 20399, Biotechnology — Ancillary materials present during the production of cellular therapeutic products
ISO 20688-2, Biotechnology — Nucleic acid synthesis — Part 2: General definitions and requirements for the production and quality control of synthesized gene fragment, gene, and genome
ISO 4307, Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for saliva — Isolated human DNA
EN ISO 20166-4, Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO/DIS 20166-4:2020)
ISO 15189, Kliniska laboratorier - Särskilda krav på kvalitet och kompetens
ISO/TR 3985, Biotechnology - Data Publication - Preliminary Considerations and Concepts
ISO 5058-1, Biotechnology — Genome Editing — Part 1: Terminology
ISO/TS 23494-1, Biotechnology — Provenance information model for biological material and data — Part 1: Design Concepts and General Requirements
ISO 24421, Biotechnology — Minimum requirements for optical signal measurements in photometric methods for biological samples
ISO 24420, Biotechnology — Massively parallel DNA sequencing — General Requirements for Data Processing of Shotgun Metagenomics
ISO 18113-1, In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
ISO 18113-2, In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
ISO 18113-3, In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
ISO 18113-4, In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
EN ISO 4307, Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated DNA
ISO 20776-3, Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 3: Part 3: Disc-diffusion agar reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases
EN ISO 20184-3, Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO/DIS 20184-3:2020)
ISO 5441, Competence of Biorisk Management Advisors
ISO 16256, In vitro diagnostik - Laboratoriemedicin och system för in vitro-diagnostiska undersökningar - Referensmetod för provning av in vitro-aktiviteten hos antimikrobiella ämnen mot jästsvampar inom infektionssjukdomar
EN ISO 23118, Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
EN ISO 23162, Basic semen examination - Specification and test methods (ISO/DIS 23162:2020)
ISO 20776-2, In vitro diagnostik - Laboratoriemedicin och system för in vitro-diagnostiska undersökningar - Bestämning av mikroorganismers känslighet för antimikrobiella medel och utvärdering av utrustning för känslighetsbestämning - Del 2: Utvärdering av prestanda hos utrustning för känslighetsbestämning
EN ISO 6717, In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020)
ISO/TS 5798, Quality Practice for detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods
ISO 24088-1, Biotechnology — Biobanking — Requirements for the collection, processing, storage and transportation of microorganisms — Part 1: Bacteria and archaea
