Redacted Version definition

Redacted Version means this Agreement and its Schedules other than Schedule 2 (The Initial Consenting Creditors), Part 1 (Initial Backstop Parties) of Schedule 4 (Backstop Parties and Undertakings) and the signature pages of the Initial Consenting Creditors to this Agreement.

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Redacted Version means a version of the proposal with the information considered confidential as defined by NMAC 1.4.1.45 and defined herein and outlined in Section II.C.8 of this RFP blacked out BUT NOT omitted or removed.

Redacted Version has the meaning set forth in Section 7.4.2.

Examples of Redacted Version in a sentence

• These two (2) identical CDs should be entitled “For Public Release: Redacted Version of [Name of Vendor]’s Proposal and Exhibits.

• Notwithstanding the foregoing, MorphoSys shall be permitted to take any action in order to comply with any applicable law, EXECUTION COPY (Redacted Version) CONFIDENTIAL regulation or court order in any proceeding that is not initiated directly or indirectly by MorphoSys, whether or not such proceeding relates to any challenge or dispute concerning the validity of any AME Patent Rights in a patent office proceeding or a court of law.

• If the parties do not mutually agree on the Redacted Version within thirty (30) days after the Effective Date, this Seventh Amendment shall be null and void.

• The PDF should be entitled Public Release: Redacted Version of RFP/RFO/IFB solicitation No.

• If the parties do not mutually agree on the Redacted Version within thirty (30) days after the Effective Date, this Sixth Amendment shall be null and void.

• Sixty per cent of the victims were men, see ‘Public Redacted Version Of Corrigendum to the Report on Victims’ Representations (ICC-01/09-17-Conf-Exp- Corr) and annexes 1 and 5’ (29 March 2010) ICC-01/09-17-Corr-Red, paras 40-45.

• NDEE over £1 Milllion Projects Framework Centrica Business Solutions UK Limited - Open Contracting Redacted Version minus Schedule 5 1.

• The Employer will assign bargaining unit work to bargaining unit employees only, except in case of emergency.

• In order for Licensee to comply with the Act on Registration of Agreements, WDCL shall provide Licensee with Redacted Version of this first amendment sent via email within five (5) business days of the execution date of this first amendment in order for such Redacted Versions to be disclosed.

• In the event that the sum of such variations is greater than [****] percent ([**]%) but less than, or equal to, [*******] percent ([**]%), then such target shall be considered partially met, and the payment under Section 4.1 of this Amendment shall be reduced Redacted Version by [******************] dollars ($[*******]).

More Definitions of Redacted Version

Redacted Version has the meaning set forth in Section 9.3.3.

Redacted Version means the redacted copy of this Agreement as agreed by

Redacted Version has the meaning set forth in Section 11.3.2. 1.156 “Regulatory Approval” means all approvals of the applicable Regulatory Authority necessary for the commercial marketing and sale of a product in a country(ies), excluding any pricing and reimbursement approvals that may be required. 1.157 “Regulatory Approval Application” means: (a) a BLA; or (b) any other application to seek Regulatory Approval of a product in any country or multinational jurisdiction, as defined in applicable Laws and filed with the relevant Regulatory Authorities of such country or jurisdiction. 1.158 “Regulatory Authority” means the FDA in the United States or any Governmental Authority in another country or regulatory jurisdiction in the Territory that is a counterpart to the FDA and holds responsibility for granting Regulatory Approval for a product in such country or regulatory jurisdiction, including the EMA and PMDA, and any successor(s) thereto. 1.159 “Regulatory Exclusivity” means any exclusive marketing rights or data exclusivity rights conferred by any Regulatory Authority with respect to any Product, excluding Patent Rights, that precludes the use of any clinical data collected and filed for such Product for the benefit of any Regulatory Approval for a generic or biosimilar product (for any use), including orphan or pediatric exclusivity where applicable. 1.160 “Regulatory Filing” means, with respect to a product, any documentation comprising any filing or application with any Regulatory Authority with respect to such product, or its use or potential use in the Field, any document submitted to any Regulatory Authority, including any IND and any Regulatory Approval Application, and any correspondence to, from or with any Regulatory Authority with respect to such product (including minutes of any meetings, telephone conferences or discussions with any Regulatory Authority). 1.161 “Reimbursable Costs” has the meaning set forth in Section 4.1.1. 1.162 “Related Third-Party IP” has the meaning set forth in Section 5.2.2. 1.163 “Representatives” means a Party’s or its Affiliate’s officers, directors, employees, contractors, consultants, agents and other representatives. 1.164 “Royalty Term” has the meaning set forth in Section 8.4.

Redacted Version has the meaning set forth in Section 8.4(b). 1.79 “Registration Application” means any filing(s) made with the Regulatory Authority in any country or jurisdiction in the Territory to obtain Regulatory Approval for the Commercialization of a product in such country or jurisdiction, including an NDA in the United States. 1.80 “Regulatory Approval” means, with respect to any country in the Territory, the registrations, authorizations and approvals of the applicable Regulatory Authority that are required for Commercialization of pharmaceutical products in such country (but excluding any Pricing Approvals). 1.81 “Regulatory Authority” means, in a particular country or jurisdiction in the Territory, any applicable Governmental Authority involved in granting approval (a) to initiate or conduct clinical testing in humans, (b) for issuing the authorizations, approvals, licenses, permits, consents, registrations and filings necessary for the commercialization of a product in a country in the Territory including marketing authorizations and manufacturing licenses, or (c) to the extent required in such country or jurisdiction, for Pricing Approval for a product in such country or jurisdiction. 1.82 “Representatives” means, with respect to a Person, such Person’s officers, directors, employees, consultants, agents or other representatives.