The National Clause Samples
The National clause typically designates a specific national entity, authority, or standard that is relevant to the agreement or contract. In practice, this clause may identify which country's laws, regulations, or standards will govern certain aspects of the contract, or it may specify a national organization responsible for oversight or compliance. Its core function is to provide clarity and certainty regarding the national context or authority that applies, thereby reducing ambiguity and potential disputes over jurisdiction or applicable standards.
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The National. Red Cross Societies disseminate and assist their Governments, as auxiliaries to their public authorities in the humanitarian field, in disseminating International Humanitarian Law. They take initiatives in this respect. They disseminate the principles and ideals of the Movement and assist those governments which also disseminate them. They also cooperate with their governments to ensure respect for International Humanitarian Law.
The National. Land Commission shall be representative and independent. The composition of the membership and terms of appointment of the National Land Commission shall be set by the legislation constituting it. The Chairperson of the National Land Commission shall be appointed by the Presidency.
The National. Grievance Committee may decide a case upon transcripts, minutes and records of the Committee previously considering the case, if any. The Committee may, in any specific case, by a majority vote, agree upon other methods and procedures by which additional evidence may be obtained. In the hearing of cases, each party will submit a written statement of all facts involved in each case at the time of the hearing. If such written statement is not submitted to the Committee at the time of the hearing, the case will not be heard. Except in cases of discharge or suspension, the Union shall present its summary first. Only authorized employees of the Union and the Employer shall be permitted to participate in the presentation and hearing of cases covered by these Rules of Procedure. Arguments on the case can be cut off by majority vote after all factual information is presented. Each side shall have one opportunity for rebuttal. Cross-examination shall only come through, or by Panel members. The Panel will go into executive session and render a decision after each case has been presented. The Committee will mail in each case, or recall the parties for an announcement of the decision. The National Grievance Committee shall have the authority to refer matters to Subcommittees for investigation and report, as directed, to the National Grievance Committee. Decisions on the National Grievance Committee shall be final and binding upon all parties.
The National. Coordinating Centre shall ensure that Study Drug provided by the Coordinating Sponsor is exclusively used for the Study. The National Coordinating Centre shall ensure that Sites keep an up to date written record of the Study Drug supplied.
The National. Coordinating Centre shall ensure that publications acknowledge the financial support received for the Study from its funder(s).
The National. Coordinating Centre shall promptly notify the Coordinating Sponsor of a Site Investigator is suspected of non-compliance with section 2.3
The National. Coordinating Centre shall provide the personal details including but not limited to name, of the National Coordinating Investigator and all Site Principal Investigators and relevant employees supporting the Study and shall obtain the consent of all such persons for the Coordinating Sponsor and third parties involved in the Study to use the personal data for any purpose permitted by law.”
2.1.17 Inserting an additional clause after the existing clause 11.6 as follows: “The National Coordinating Centre represents and warrants to the Coordinating Sponsor that to the best of the National Coordinating Centre’s knowledge, neither the National Coordinating Investigator, Site Principal Investigator or any Sub-Contractor has been debarred by a regulatory authority including the FDA pursuant to its authority under Sections 306(a) and (b) of the U.S. Food, Drug and Cosmetic Act (21 U.S.C. § 335(a)) (“FDC Act”) or is the subject of any investigation or proceeding which may result in debarment by the FDA.”
2.1.18 Inserting an additional clause after the existing clause 13.19 as follows:
2.1.19 Deleting Schedule 1 in its entirety and replacing it with the annexed Schedule 3:
2.1.20 Deleting the definition of “Standard Contractual Clauses” in paragraph 1 in Schedule 3 in its entirety.
2.1.21 Deleting paragraph 2.6 in schedule 3 in its entirety.
2.1.22 Updating Appendix 1 by adding the following to the breakdown of Personal Data to be collected, as follows: “Investigator’s Financial Disclosure”
2.1.23 Deleting the Standard Contractual Clauses from the Contract in its entirety.
2.1.24 Adding Schedule 4 to the Contract as annexed to this Agreement at Schedule 2.
3 The existing Clauses, Sub-Clauses, and clause referencing of the Contract shall be re-numbered to take account of the deletions, amendments and/or additions set out above.
4 The amendments set out in this Agreement shall have effect from the date of this Agreement. 5 Unless expressly amended by this Agreement, the Contract shall remain in full force and effect.