Skip to main content
v2026.11,610 entries · CC-BY 4.0

v2026.1 · 1686 entries

Browse the Dictionary

Filter by domain, track, or full-text. Every entry is citable and CC-BY 4.0.

Showing 48 of 1686 matching entries (1686 total)

Dictionary termProposed

NIH AI Policy

NIH AI policy is not one document but three separate NIH Guide notices, each governing a different actor at a different stage of the grant lifecycle: NOT-OD-23-149 (June 2023) prohibits NIH scientific peer reviewers from using generative AI tools to analyze…

Generative AI use and disclosure· Contribution
Dictionary termProposed

Sale-Leaseback (Equipment)

An equipment sale-leaseback is a two-part transaction, executed together, in which an institution that already owns a piece of equipment (1) sells it to a buyer-lessor at fair market value and (2) immediately leases the same equipment back for continued…

Compliance and regulatory· Compliance
Dictionary termProposed

Ancillary Materials in Cell Therapy Manufacturing

A raw material used during the manufacture of a cell, gene, or tissue-engineered product that contacts the cells or construct during processing but is not intended to remain in the final product administered to the patient (e.g., growth factors, cytokines,…

clinical-research· Contribution
Dictionary termProposed

Temperature Monitoring Alarm

A temperature monitoring alarm is the notification component of a temperature monitoring system: the function that detects a monitored storage condition moving outside its defined safe range and actively alerts a responsible person, rather than simply…

Compliance and regulatory· Compliance
Dictionary termProposed

21 CFR Part 11 Temperature Monitoring

A temperature-monitoring system (freezer, refrigerator, incubator, or cold-room monitor) is accurately called "21 CFR Part 11 compliant" only when its electronic records -- and any electronic signatures applied to them -- meet 21 CFR Part 11 Subpart B/C…

Compliance and regulatory· Compliance
Dictionary termProposed

Thermal Cycler Specifications

<p>Thermal cycler specifications are the documented set of performance parameters &mdash; block format and sample capacity, ramp rate, temperature accuracy and uniformity, gradient range, lid control, and connectivity/data-logging features &mdash; that a…

Life sciences and biology· Contribution
Dictionary termProposed

Scientific Data Management System (SDMS)

A scientific data management system (SDMS) is laboratory software that automatically captures, indexes, and archives electronic data files generated by lab instruments (chromatography, spectroscopy, balances, plate readers, raw instrument logs) in their…

Compliance and regulatory· Compliance
Dictionary termProposed

True Lease vs. Finance Lease

A true lease (an operating lease under ASC 842) is an equipment lease where the lessor retains ownership for tax purposes, claims depreciation, and bears residual-value risk; the lessee simply expenses rental payments and, if there is a purchase option, it is…

Funding lifecycle and financial vocabulary· Assessment
Dictionary termProposed

Veterinary Cytology

<p><strong>Veterinary cytology</strong> is the diagnostic technique of collecting, preparing, staining, and microscopically examining individual cells (rather than intact tissue architecture, as in histopathology) obtained from an animal by fine-needle…

Compliance and regulatory· Compliance
Dictionary termProposed

ELAP Certification (Environmental Laboratory Accreditation Program)

A laboratory holds ELAP certification when California's State Water Resources Control Board (Division of Drinking Water) has accredited it for specific matrix/analyte/method combinations, called "fields of accreditation," allowing it to perform environmental…

Compliance and regulatory· Compliance
Dictionary termProposed

What Is A2LA? American Association for Laboratory Accreditation Explained

A2LA (American Association for Laboratory Accreditation) is a US-based, nonprofit, third-party accreditation body, founded in 1978, that formally recognizes a testing/calibration laboratory, medical laboratory, inspection body, biobank, or certification body…

Compliance and regulatory· Compliance
Dictionary termProposed

Tier II Reporting Software

Tier II reporting software is compliance software purpose-built to compile a facility's hazardous chemical inventory into the data fields, threshold calculations, and submission format required under EPCRA Section 312 (40 CFR Part 370), and to generate or…

Compliance and regulatory· Compliance
Dictionary termProposed

Colilert

Colilert is a defined-substrate technology (DST) reagent, manufactured by IDEXX Laboratories, used to simultaneously detect and enumerate total coliform bacteria and Escherichia coli (E. coli) in a single water sample. A test is correctly described as…

Compliance and regulatory· Compliance
Dictionary termProposed

Types of Equipment Leases

An equipment lease type is defined by two independent things: (1) the commercial end-of-term structure the vendor or leasing company offers -- fair market value (FMV), $1 buyout, 10% option, or Terminal Rental Adjustment Clause (TRAC) -- which determines…

Funding lifecycle and financial vocabulary· Assessment
Dictionary termProposed

TRAC Lease (Terminal Rental Adjustment Clause)

A TRAC lease is a motor-vehicle lease governed by IRC Section 7701(h)'s terminal rental adjustment clause exception: the lessee guarantees the vehicle's end-of-term residual value and pays (or is credited) the difference between that guaranteed figure and the…

Compliance and regulatory· Compliance
Dictionary termProposed

Scale vs Balance

A scale is a general-purpose weighing instrument (commonly strain-gauge based) optimized for capacity and ruggedness with coarser readability, while a balance is a precision weighing instrument (traditionally comparative, now typically electromagnetic force…

Compliance and regulatory· Compliance
Dictionary termProposed

What Is ANAB? ANSI National Accreditation Board Explained

ANAB (the ANSI National Accreditation Board) is a US laboratory and certification-body accreditation organization, operated as a subsidiary of ANSI, that formally recognizes a testing/calibration laboratory, medical laboratory, inspection body, biobank, or…

Compliance and regulatory· Compliance
Dictionary termProposed

Xeno-Free Media

Xeno-free (XF) media is cell-culture medium formulated to contain no components derived from a species other than the one being cultured, used to eliminate the risk of xenogeneic contamination (viral, prion, and immunogenic non-human antigens) that comes with…

Compliance and regulatory· Compliance
Dictionary termProposed

Unique Molecular Identifiers (UMIs)

Short, random or semi-random nucleotide sequences (typically 6-12 base pairs) added to individual DNA or RNA fragments during next-generation sequencing (NGS) library preparation, before PCR amplification, so that reads descended from the same original…

Life sciences and biology· Contribution
Dictionary termProposed

Cryo-EM Microscope

A cryo-EM microscope is a transmission electron microscope purpose-built or fitted with an integrated cryogenic specimen workflow -- a cryo-transfer/autoloader system, a stable cryo-stage held below devitrification temperature, a field emission electron…

Life sciences and biology· Contribution
Dictionary termProposed

SEFA 8 (Laboratory Fume Hoods Recommended Practice)

SEFA 8 is the Laboratory Fume Hoods Recommended Practice published by the Scientific Equipment and Furniture Association (SEFA), setting construction requirements and tracer-gas containment/face-velocity test protocols (As-Manufactured, As-Installed, As-Used)…

Compliance and regulatory· Compliance
Dictionary termProposed

PhiX Control

PhiX control (PhiX Control v3) is an adapter-ligated sequencing library derived from the bacteriophage PhiX174 genome, spiked into Illumina NGS runs at a defined percentage to calibrate base-calling and error-rate metrics, and, at higher spike-in levels, to…

Life sciences and biology· Contribution
Dictionary termProposed

Single-Use Assemblies (SUAs)

A single-use assembly (SUA) is a pre-fabricated, pre-sterilized fluid-path component -- typically some combination of flexible tubing, bags, connectors, filters, and sensors -- manufactured, irradiated, and supplied ready to install into a bioprocess for…

Compliance and regulatory· Compliance
Dictionary termProposed

Chemically Defined Media (CDM)

Chemically defined media (CDM) is a cell-culture growth medium in which every component -- salts, amino acids, vitamins, lipids, and any protein supplements -- is a known, individually specified chemical entity added at a documented concentration, with no…

Compliance and regulatory· Compliance
Dictionary termProposed

Chemical Safety Software

<p>Chemical safety software is a category of purchased or subscribed platforms that help a lab, facility, or manufacturer manage the compliance obligations that come with owning, using, or producing hazardous chemicals. In procurement terms, a product…

Compliance and regulatory· Compliance
Dictionary termProposed

Glove Compatibility Chart

A glove compatibility chart is a reference table, published by a glove manufacturer, distributor, or standards body, rating a specific glove product's resistance to specific named chemicals, typically as a breakthrough-time-based class (ANSI/ISEA 105's 0-6…

Compliance and regulatory· Compliance
Dictionary termProposed

NELAC (National Environmental Laboratory Accreditation Conference)

NELAC (National Environmental Laboratory Accreditation Conference) was the multi-state, EPA-supported effort that created the original national standard for accrediting environmental testing laboratories, replacing separate state-by-state certification…

Compliance and regulatory· Compliance
Dictionary termProposed

Fetal Bovine Serum (FBS)

Fetal bovine serum (FBS), also called fetal calf serum (FCS), is the liquid fraction of blood collected from bovine fetuses at slaughter, clarified and filtered for use as a growth-supporting supplement added to basal cell-culture media (typically 5-10% of…

Compliance and regulatory· Compliance
Dictionary termProposed

Eyewash Station

<p>An eyewash station is emergency safety equipment that delivers a controlled, hands-free stream of flushing fluid to a person's eyes (or eyes and face) to remove a hazardous substance following an accidental exposure. In U.S. laboratory and facility…

Compliance and regulatory· Compliance
Dictionary termProposed

Nitrile Glove Sizing: Chart, Fit, and Facility Size-Mix

Nitrile glove sizing is the mapping between a glove's dimensional designation (XS through XXL) and hand-circumference measurements, used both to fit an individual wearer and, for institutional buyers, to translate a facility's hand-size distribution into a…

Compliance and regulatory· Compliance
Dictionary termProposed

Nitrile Glove Thickness (Mil)

Nitrile glove thickness in mils measures the gauge of the glove material -- one mil equals 0.001 inch (0.0254 mm) -- and is reported per point on the glove (fingertip, palm, cuff) because dipped-glove manufacturing, the standard nitrile exam-glove process…

Compliance and regulatory· Compliance
Dictionary termProposed

Procurement Card (P-Card)

A procurement card (P-card, used interchangeably with 'purchasing card') is a commercial charge or credit card an institution issues to a named individual for direct, point-of-sale purchases within defined transaction and monthly limits, reconciled centrally…

Compliance and regulatory· Compliance
Dictionary termProposed

Central Stores

A centralized institutional department -- part of a university's or hospital's supply chain, procurement, or facilities organization -- that receives, inspects, warehouses, and internally distributes commonly used supplies, chemicals, and equipment to the…

Compliance and regulatory· Compliance
Dictionary termProposed

Simplified Acquisition Threshold (SAT)

The simplified acquisition threshold (SAT) is the dollar ceiling, set in FAR 2.101 and cross-referenced by 2 CFR 200.1 for federal grant recipients, up to which a buyer may use streamlined, informal purchasing procedures instead of formal sealed bidding or a…

Compliance and regulatory· Compliance
Dictionary termProposed

GPO Administrative Fee

A GPO administrative fee is the percentage-based payment a vendor makes to a group purchasing organization (GPO), tied to the volume of purchases its member institutions make under that vendor's GPO contract, which the GPO retains to fund its own contracting…

Compliance and regulatory· Compliance
Dictionary termProposed

What Is a DICOM Conformance Statement?

A DICOM conformance statement is a vendor-published document, structured per DICOM PS3.2 (Conformance), that specifies exactly which SOP (Service-Object Pair) classes a medical-imaging device or software supports and in which network role (SCU or SCP), which…

clinical-research· Contribution
Dictionary termProposed

ECCN (Export Control Classification Number)

An Export Control Classification Number (ECCN) is a five-character alphanumeric code assigned to an item, software package, or technology when it matches a specific entry on the US Commerce Control List (CCL) under the Export Administration Regulations (EAR,…

Research security· Compliance
Dictionary termProposed

CGA Pamphlet P-1

<p>CGA Pamphlet P-1 (<em>Safe Handling of Compressed Gases in Containers</em>) is the Compressed Gas Association's industry consensus standard covering the in-plant handling, storage, and use of compressed gas cylinders, portable tanks, and similar…

Compliance and regulatory· Compliance
Dictionary termProposed

CGA Fittings

A CGA fitting is the standardized valve outlet/regulator inlet connection, identified by a CGA (Compressed Gas Association) three-digit number under CGA V-1 / ANSI B57.1, that is matched to a specific gas or group of compatible gases so that a regulator built…

Compliance and regulatory· Compliance
Dictionary termProposed

USP Class VI Certification

USP Class VI certification is a designation that a specific plastic material or component has passed the most stringent tier of biological reactivity testing under United States Pharmacopeia (USP) General Chapter <88>, "Biological Reactivity Tests, In Vivo."…

Compliance and regulatory· Compliance
Dictionary termProposed

Type I Borosilicate Glass

Type I borosilicate glass is a pharmaceutical primary-packaging glass classified under USP General Chapter <660>, Containers—Glass, as meeting the highest hydrolytic-resistance category through borosilicate composition and a passing result on the chapter's…

Compliance and regulatory· Compliance
Dictionary termProposed

Biospecimen

A biospecimen is a biological material — such as blood, tissue, urine, saliva, or a derived product like extracted DNA/RNA, plasma, or a cell line — that has been collected from a human or other living source and preserved under a documented chain of custody…

clinical-research· Contribution
Dictionary termProposed

EAR99 Classification

EAR99 is the residual classification for an item, software, or technology that is subject to the US Export Administration Regulations (EAR, 15 CFR 730-774) but matches no specific Export Control Classification Number (ECCN) entry on the Commerce Control List…

Research security· Compliance
Dictionary termProposed

Vendor Neutral Archive (VNA)

A vendor neutral archive (VNA) is a medical-imaging storage architecture that ingests, indexes and stores diagnostic images and related clinical content in standard formats (typically DICOM for images, non-DICOM objects via XDS-style wrapping) with…

Research data infrastructure· Identifiers
Dictionary termProposed

What Is a Radiology Information System (RIS)?

A radiology information system (RIS) is the software that manages a radiology or imaging department's operational workflow around an exam — patient scheduling and registration, order/accession tracking from request through signed report, radiologist reporting…

clinical-research· Contribution
Dictionary termProposed

cGMP Facility

A cGMP facility is a drug, biologic, device, or API manufacturing site that meets FDA's current Good Manufacturing Practice regulations (21 CFR Parts 210/211 for drugs; Part 600-series provisions for biologics; Part 820/QMSR for devices; ICH Q7 for APIs)…

clinical-research· Contribution
Dictionary termProposed

ANSI/AIHA Z9.5 (Laboratory Ventilation)

ANSI/AIHA Z9.5 ("Laboratory Ventilation") is the American National Standards Institute-approved consensus standard, developed and maintained by AIHA (the American Industrial Hygiene Association), that specifies engineering and performance criteria for…

Compliance and regulatory· Compliance
Dictionary termProposed

GMP Facility

A GMP facility is a manufacturing, packaging, testing, storage, or distribution site that is designed, qualified, and operated to meet Good Manufacturing Practice requirements applicable to its product type (21 CFR Part 211 for finished drugs, ICH Q7 for…

Compliance and regulatory· Compliance

Referenced across the research world

University of Cambridge logoColumbia University logoCrossref logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logoUniversity of Cambridge logoColumbia University logoCrossref logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logo
  • University of Cambridge logo
  • Columbia University logo
  • Crossref logo
  • University of Edinburgh logo
  • Harvard University logo
  • University of Oxford logo
  • Princeton University logo
  • Stanford School of Medicine logo
  • University College London logo
  • ORCID logo

View CASRAI adoption →