Clinical Trial Subject definition

Clinical Trial Subject means a person recruited to participate in the Clinical Trial.

Clinical Trial Subject means a subject, whether healthy volunteer or patient, in the Clinical Trial;

Clinical Trial Subject means a person enrolled to participate in the Clinical Trial according to criteria detailed in the Protocol; Confidential Information means all confidential information (however recorded or preserved) disclosed by a Party and/or its Affiliate (as defined above) to the other Party in connection with the Clinical Trial which is information that would be regarded as confidential by a reasonable business person relating to the business, affairs, plans, intentions or market opportunities of the disclosing Party and/or its Affiliate, including (but not limited to): the operations, processes, product information, designs, trade secrets or Know-How of the disclosing party any information developed by the Parties in the course of carrying out this Agreement in the case of Sponsor Confidential Information, the Protocol, the Investigator Brochure(s) relating to the Clinical Trial and Appendix 4 to this Agreement (‘Financial Arrangements’);

Examples of Clinical Trial Subject in a sentence

• Any right or remedy of a third party which existed or is available apart from the Third Party Rights Act is not affected; in particular, without limitation, any right of any Clinical Trial Subject to claim compensation in accordance with the Clinical Trial Compensation Guidelines referred to in Appendix 4.

• Personal data (as defined in the Data Protection Act 1998) shall not be disclosed to the Sponsor or CRO by the Trust save where this is required to satisfy the requirements of the Protocol or for the purpose of monitoring or adverse event reporting, or in relation to a claim or proceeding brought by the Clinical Trial Subject in connection with the Clinical Trial.

• Neither the Sponsor nor CRO shall disclose the identity of Clinical Trial Subjects to third parties without prior written consent of the Clinical Trial Subject, except in accordance with the provisions of the Data Protection Act 1998 and the principles set out in the NHS Confidentiality Code of Practice (November 2003), unless in relation to a claim or proceeding brought by the Clinical Trial Subject in connection with the Clinical Trial.

• The Sponsor shall not disclose the identity of Clinical Trial Subjects to third parties without prior written consent of the Clinical Trial Subject, except in accordance with the provisions of the Data Protection Act 1998 and the principles set out in the NHS Confidentiality Code of Practice (November 2003), unless in relation to a claim or proceeding brought by the Clinical Trial Subject in connection with the Clinical Trial.

• The Sponsor shall not disclose the identity of Clinical Trial Subjects to third parties without prior written consent of the Clinical Trial Subject, except in accordance with the provisions of the Data Protection Act 1998 and the principles set out in the NHS Scotland Code of Practice on Protecting Patient Confidentiality (August 2003), unless in relation to a claim or proceeding brought by the Clinical Trial Subject in connection with the Clinical Trial.

More Definitions of Clinical Trial Subject

Clinical Trial Subject means a person enrolled to participate in the Clinical Trial according to criteria detailed in the Protocol; Confidential Information means all confidential information (however recorded or preserved) disclosed by a Party and/or its Affiliate to another Party, in connection with the Clinical Trial, which is information that would be regarded as confidential by a reasonable business person, including (but not limited to): business, affairs, plans, intentions or market opportunities operations, processes, product information, designs, trade secrets or Know-How any information developed by the Parties in connection with the Clinical Trial in the course of carrying out this Agreement the Protocol, the Investigator Brochure(s) relating to the Clinical Trial and Appendix 4 to this Agreement (‘Financial Arrangements’);

Clinical Trial Subject means A patient who consents to take part in the Study

Clinical Trial Subject means a person enrolled at any time in a Clinical Trial (whether or not that person meets all eligibility criteria for enrolment into the Clinical Trial set out in any Trial Protocol or otherwise).

Clinical Trial Subject an individual who participates in the Clinical Trial as a recipient of the Product, some other treatment or product, or without receiving any treatment or product (as a control). CHDR2227-AGN-188-1 29 Jul. 22 Page 2 of 20 "Competent Authority": any local or national agency, court, authority, department, inspectorate, minister, ministry official or public or statutory person of, or of any government of, any country having jurisdiction over the Agreement, either of the Parties, or the development or marketing of medicinal products.

Clinical Trial Subject means a person who is enrolled in a Clinical Trial, whether or not that person meets all eligibility criteria for enrolment into the Clinical Trial set out in any Trial Protocol or otherwise.

Clinical Trial Subject or “Subject” means an individual, whether a patient or not, who participates in the Clinical Trial as a recipient of Investigational Medicinal Product.

Clinical Trial Subject means a person participating in a Clinical Trial.