Foreign Equivalent definition

Foreign Equivalent means the completion of the milestones in a foreign major market country such as the United Kingdom, Japan, Germany, Canada, etc.

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Foreign Equivalent means the performance or occurrence of activities in non-U.S. jurisdictions similar to the performance or occurrence of activities in the United States covered by the terms “Clinical Trial,” “Phase II Clinical Trial,” “Completion of a Phase II Clinical Trial,” “Phase III Clinical Trial,” “Completion of a Phase HI Clinical Trial,” “IND,” “NDA,” “Submit an NDA” “NDA Approval,” and “Regulatory Approval,” as each such term is defined in this Article.

Foreign Equivalent means the performance or occurrence of activities in non-U.S. jurisdictions similar to the performance or occurrence of activities in the United States covered by the terms “Clinical Trial,” “Regulatory Clearance”, “510(k) Clearance”, “PMA” and “Regulatory Approval,” as each such term is defined in this Article.

Examples of Foreign Equivalent in a sentence

• Mallinckrodt shall include MBI as an alternative manufacturing site, as Mallinckrodt deems necessary or as required, in all relevant submissions and applications to Foreign Equivalent Authorities.

• MBI shall have the right to review and approve any application or submission to Foreign Equivalent Authorities by Mallinckrodt pursuant to this SECTION 2.01(e) prior to submission to Foreign Equivalent Authorities, which approval shall not be unreasonably withheld or delayed.

• Mallinckrodt shall not be required to obtain any approval which Nycomed has obtained or which it is required to obtain under the Nycomed Agreement, if (i) Mallinckrodt is permitted by the applicable Foreign Equivalent Authorities to reference the approval or if it otherwise has or acquires the benefit of the approval and (ii) where the approval has not yet been obtained, Nycomed, is proceeding diligently to obtain the approval (as determined by Mallinckrodt in its judgment, after consultation with MBI).

• Clinical trials and other studies shall be conducted in accordance with applicable FDA (or Foreign Equivalent Authorities') requirements and procedures, including but not limited to Good Laboratory Practices and Good Clinical Practices (as those terms are defined pursuant to industry standards).

• A Supplemental Tranche with aggregate commitments from the Supplemental Lender in Foreign Equivalent amount of $ .

• Within sixty (60) months of the Election Amendment Effective Date, Licensee shall initiate Phase II Clinical Trials (or Foreign Equivalent) of a Diagnostic Licensed Product if necessary.

• For purposes of this Section, Foreign Equivalent Patents shall be patents based upon the disclosures in the patents listed on Exhibit A hereto and claiming identical or equivalent inventions.

• Cosmo shall provide Salix with the status of such Foreign Equivalent Patents and Salix Licensed Patents no less frequently than once per every semi-annual period.

• If on a given day an unfilled vacancy exists and a substitute is not available and an administrator assigns those students to be divided between two or three other teachers, this will result in compensation for each teacher as follows: Number of classrooms: Half Day Pay for Each Teacher: Full Day Pay for Each Teacher: 1 $67.50 $135 2 $33.75 $67.50 3 $22.50 $45 Nothing will be compensated at less than half a day, with the exception of teachers who are covering during their plan period.

• A Supplemental Tranche with aggregate commitments from the Supplemental Lender in Foreign Equivalent amount of $____________.

More Definitions of Foreign Equivalent

Foreign Equivalent means the performance or occurrence of activities in non-U.S. jurisdictions similar to the performance or occurrence of activities in the United States covered by the terms “Clinical Trial,” “Initiate Phase I Clinical Trial,” “Complete Phase I Clinical Trial,” “Phase II Clinical Trial,” “Initiate Phase II Clinical Trial,” “Complete Phase II,” “Phase III Clinical Trial,” “Initiate Phase III Clinical Trial,” “Complete Phase III Clinical Trial,” “BLA,” “BLA Approval,” and “Regulatory Approval,” as each such term is defined in this Article.

Foreign Equivalent means activities or approvals outside the United States that are similar to activities or approvals covered by “Clinical Trial”, “FDA”, “IND”, “Phase I Clinical Trial”, “Phase II Clinical Trial”, “Phase III Clinical Trial”, “NDA”, and “NDA Approval”.

Foreign Equivalent means the performance or occurrence of activities in non-U.S. jurisdictions similar to the performance or occurrence of activities in the United States covered by the terms “Clinical Trial,” “Initiate Phase I Clinical Trial,” “Phase II Clinical Trial,” “Initiate Phase II Clinical Trial,” “Phase III Clinical Trial,” “Initiate Phase III Clinical Trial,” “IND” and “Regulatory Approval,” as each such term is defined in this Article.

Foreign Equivalent means the performance or occurrence of activities in non-U.S. jurisdictions similar to the performance or occurrence of activities in the United States covered by the terms “Clinical Trial,” “Initiation of Phase I Clinical Trial,” “Completion of Phase I Clinical Trial,” “Phase II Clinical Trial,” “Initiation of Phase II Clinical Trial,” “Completion of Phase II,” “Phase III Clinical Trial,” “Initiation of Phase III Clinical Trial,” “Completion of Phase III Clinical Trial,” “NDA,” “Market Exclusivity Period,” “NDA Approval,” and “Regulatory Approval,” as each such term is defined in this Section.