PSC Register definition
PSC Register means the “PSC register” within the meaning of section 790C(10) of the Companies ▇▇▇ ▇▇▇▇.
PSC Register means “PSC register” within the meaning of section 790(c)(10) of the Companies Act 2006.
PSC Register means the register of people with significant control required to be maintained by an entity pursuant to Part 21A of the Companies ▇▇▇ ▇▇▇▇ or the “central register” maintained by Companies House where an entity has elected for its register to be kept by Companies House.
Examples of PSC Register in a sentence
In the event that the Company is legally required to comply with Part 21A of the Companies Act 2006, to the extent not available from public records at Companies House, a copy of the PSC Register of the Company (provided that, for the avoidance of doubt, such PSC Register shall not be required to be in a form and substance satisfactory to the Interim Facility Agent).
Attached thereto is a certified copy of the PSC Register of each such Loan Party whose share capital is subject to security created under any U.K. Security Document.
Guidance on the new PSC Register is just one of the things Cthhatinsmaall businesses need to understand.
All minute books and statutory books and registers of the Company (including the register of members, the register of people with significant control (PSC Register), all certificates of incorporation, articles of association, other Constitutive Documents and (if applicable) common seal(s)) duly written up to date shall have been delivered to Buyer or confirmation in writing that the same is in the possession of the Company as at Closing.
More Definitions of PSC Register
PSC Register means the Register of Persons with Significant Control of relevant companies established by the Registrar under section 372;
PSC Register means “PSC register” within the meaning of section 790C(10) of the Companies Act 2006 of the Parliament of the United Kingdom.
PSC Register means the “PSC register” within the meaning of section 790C(10) of the Companies Act 2006. “Qualified Cash” means an amount equal to (a) the amount of Borrower’s Cash held in accounts subject to an Account Control Agreement in favor of Agent, minus (b) the Qualified Cash A/P Amount. “Qualified Cash A/P Amount” means the amount of ▇▇▇▇▇▇▇▇’s accounts payable under GAAP not paid after the 90th day following the invoice for such account payable. “Receivables” means (i) all of Borrower’s Accounts, Instruments, Documents, Chattel Paper, Supporting Obligations, letters of credit, proceeds of any letter of credit, and Letter of Credit Rights, and (ii) all customer lists, software, and business records related thereto. “Registration” means any registration, authorization, approval, license, permit, clearance, certificate, and exemption issued or allowed by any governmental authority that is necessary for Borrower or any of its Subsidiaries to conduct its respective activities. “Required Lenders” means at any time, the holders of more than fifty percent (50%) of the sum of the aggregate unpaid principal amount of the Term Loans then outstanding. “Resolution Authority” means any body which has authority to exercise any Write-down and Conversion Powers. “Responsible Officer” means any of the Chief Executive Officer, General Counsel (or Chief Legal Officer) and Chief Financial Officer of Borrower. “Restricted License” means any material License or other similar material agreement with respect to which Borrower is the licensee (a) that prohibits or otherwise restricts Borrower from granting a security interest in Borrower’s interest in such License or agreement or any other property, or (b) for which a default under or termination of could interfere with Agent’s right to sell any Collateral. For the avoidance of doubt, “Restricted License” does not include any commercially available or open source software. “Sanctioned Country” means, at any time, a country or territory which is the subject or target of any Sanctions. “Sanctioned Person” means, at any time, (a) any Person listed in any Sanctions-related list of designated Persons maintained by the Office of Foreign Assets Control of the U.S. Department of
PSC Register has the meaning given to in s 790C of the Companies Act 2006;
PSC Register means the “PSC register” within the meaning of section 790C(10) of the Companies ▇▇▇ ▇▇▇▇. “Public Health Laws” means all Requirements of Law relating to the procurement, development, clinical and non-clinical evaluation, product approval or licensure, manufacture, production, analysis, importation, exportation, use, handling, quality, sale, labeling, promotion, clinical trial registration or post market requirements of any drug, biologic or other product (including, without limitation, any ingredient or component of the foregoing products) subject to regulation under the Federal Food, Drug, and Cosmetic Act (21 U.S.C. § 301 et seq.) and the Public Health Service Act (42 U.S.C. § 201 et seq.), including without limitation the regulations promulgated by the FDA at Title 21 of the Code of Federal Regulations, or any other FDA Laws, and all applicable regulations promulgated by the NIH and codified at Title 42 of the Code of Federal Regulations. “Products” means all products, software, service offerings, technical data or technology currently being designed, manufactured or sold by Borrower or any of its Subsidiaries or which Borrower or any of its Subsidiaries intends to sell, license, or distribute in the future including any products or service offerings under development, collectively, together with all products, software, service offerings, technical data or technology that have been sold, licensed or distributed by Borrower or such Subsidiary since formation.
PSC Register has the meaning set forth in Section 4.06(k).
PSC Register means “PSC Register” within the meaning of section 790C(10) of the Companies Act 2006. “PSC Registrable Person” means a “registrable person” or “registrable relevant legal entity”. “Public Health Law” means all Requirements of Law relating to the procurement, development, clinical and non-clinical evaluation or investigation, product approval or clearance manufacture, production, analysis, distribution, dispensing, importation, exportation, use, handling, quality, reimbursement, sale, labeling, advertising, promotion, or postmarket requirements of any drug, medical device, food, dietary supplement, or other product (including any ingredient or component of, or accessory to, the foregoing products) subject to regulation under the Federal Food, Drug and Cosmetic Act (21 U.S.C. et seq.) and similar state or foreign laws, pharmacy laws, or consumer product safety laws. “Recipient” is defined in Section 2.6(g)(ii). “Register” is defined in Section 2.8(a). “Registered Organization” means any “registered organization” as defined in the Code with such additions to such term as may hereafter be made. “Regulation” is defined in Section 13.2 -114-