Human Samples definition

Human Samples means any human tissue or human biological material of a natural person (“Donor”), including any portion of an organ, any tissue, skin, bone, muscle, connective tissue, blood, cerebrospinal fluid, cells, gametes, or sub-cellular structures such as DNA, or any derivative of such human biological material such as stem cells, cell lines or xenograft tissues; and any human biological product, including, but not limited to, hair, nail clippings, teeth, urine, faeces, breast milk, and sweat.
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Human Samples means human biological material, including any portion of any tissue, blood, cerebrospinal fluid, cells or sub-cellular structures such as DNA, or any derivative of such human biological material such as pathogens (bacteria, viruses, fungi, parasites), serum, stem cells, cell lines and any human biological product. Access to, provision and exchange of Human Samples under the Project shall be carried out pursuant to the terms of this Consortium Agreement, any Study Protocols and the following principles: only Parties that are [hospitals //or// university/university hospital] shall be allowed to permanently store Human Samples. Collected Human Samples will be aliquoted (split) into fragments of the original sample at the microbiology institutions of each Party that is a [university/university hospital]. One aliquot will be shipped to the Party/ies performing examinations such as sequencing and metabolomics as described in the Project Description and/or the respective Study Protocol. Leftover aliquots will be stored at each microbiology institution for at least 5 years; Human Samples shall not be disposed of or acquired as such for research purposes in return for payment or other non-cash advantage. However, the foregoing shall not apply to operations such as preparation, transport, storage etc. of Human Samples; The Parties may only use the Human Samples received under this Consortium Agreement for the Project and shall either return or destroy the Human Samples after the related activities to the providing Party, or if requested by the patient.
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Human Samples has the meaning set forth in Section 3.11.
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Examples of Human Samples in a sentence

  • Recipients of MSF Datasets that include Personal Data and/or Human Samples will be informed if a Data Subject withdraws its consent and will be required to delete the appropriate data rows and inform MSF in writing that this has been done.

  • In case the requested MSF Dataset contains Personal Data or Human Samples, or is subject to limits relative to the consent of Data Subjects described in article 1.2.3, the Requestor shall seek and obtain ethics approvals from HCECs and MSF ERB.

  • The decision to include specific data, datasets and/ or Human Samples will be made by the Medical Director(s) representing their own Operational Directorate(s) Custodian of such data, datasets and/ or Human Samples.

  • The date for states and provinces within major emitter developing countries should be five years from the date that compliance obligations begin under the cap-and-trade program.

  • A plan for data management and data sharing, including Human Samples, shall be included in relevant Research proposals, consistent with the policy document and the procedures laid out for managed access in section II.

  • Approval of the data sharing plan in the research proposal rests with the Medical Director(s) of the Operational Directorate(s) that are Custodian of the proposed data or Human Samples.

  • Genotyping of Giardia duodenalis Cysts by New Real-Time PCR Assays for Detection of Mixed Infections in Human Samples.

  • The Beneficiaries must use Human Samples under and pursuant to this Consortium Agreement and the Grant Agreement in compliance with their respective obligations under applicable international and national laws and regulations.

  • Appendix 1 Authority to Import Human Samples QUB-HTA-008Appendix 1 Authority to Import Human SamplesTo be completed by the Chief Investigator or Person Responsible for undertaking the import of relevant material into the University and submitted to the Designated Individual (j.james@qub.ac.uk (MBC/BCH) or g.j.mckay@qub.ac.uk (RVH)) and the Research Governance Team (researchgovernance@qub.ac.uk).

  • Martin, High-Resolution Mass Spectrometry (HRMS) Methods for Nontarget Discovery and Characterization of Poly- and Per-fluoroalkyl Substances (PFASs) in Environmental and Human Samples, TrAC, Trends Anal.


More Definitions of Human Samples

Human Samples. Section 17.4.1.4
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Related to Human Samples

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Human use means the internal or external administration of radiation or radioactive material to human beings.

  • health and safety file means a file, or other record containing the information in writing required by these Regulations "health and safety plan" means a site, activity or project specific documented plan in accordance with the client's health and safety specification;

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical substance of the Drug in bulk form prior to incorporation into the Product.

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Human trafficking means a scheme or plan to which all of the following apply:

  • Human subject means a living individual about whom an investigator (whether professional or student) conducting research:

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Samples mean representative physical examples of materials, equipment or workmanship, used to confirm compliance with requirements and/or to establish standards for use in execution of the Work.

  • health and safety specification means a site, activity or project specific document prepared by the client pertaining to all health and safety requirements related to construction work;

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Human being means a person who has been born and is alive.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Health and Safety Plan means a documented plan which addresses hazards identified and includes safe work procedures to mitigate, reduce or control the hazards identified;

  • Study means the investigation to be conducted in accordance with the Protocol.

  • Animal means any nonhuman animate being endowed with the power of voluntary action.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Home health aide means an individual employed by a home health agency to provide home health services under the direction of a registered nurse or therapist.

  • Infectious Disease means an illness that is capable of being spread from one individual to another.

  • Diagnosis means the definition of the nature of the Client's disorder. When formulating the Diagnosis of Client, CONTRACTOR shall use the diagnostic codes and axes as specified in the most current edition of the DSM published by the American Psychiatric Association. DSM diagnoses will be recorded on all IRIS documents, as appropriate.

  • Electronic Health Record shall have the same meaning as the term is defined in section 13400 of the HITECH Act (42 U.S.C. §17921(5).

  • Active Ingredient means the clinically active material(s) that provide pharmacological activity in a pharmaceutical product (excluding formulation components such as coatings, stabilizers, excipients or solvents, adjuvants or controlled release technologies).

  • Human consumption means the use of water for drinking, bathing or showering, hand washing, oral hygiene, or cooking, including, but not limited to, preparing food and washing dishes.

  • Grab sample means an individual sample collected in less than 15 minutes in conjunction with an instantaneous flow measurement.

  • Contractor Materials means Materials owned or developed prior to the provision of the Work, or developed by Contractor independently from the provision of the Work and without use of the Court Materials or Confidential Information.