Pharmaceutical Laws definition

Pharmaceutical Laws means federal, state and local laws, rules or regulations, codes, orders, decrees, judgments or injunctions issued, promulgated, approved or entered, relating to dispensing, storing or distributing prescription medicines or products, including laws, rules or regulations relating to the qualifications of Persons employed to do the same.
Pharmaceutical Laws has the meaning set forth in Section 3.7(b).
Pharmaceutical Laws means Laws primarily regulating the testing, clinical trials, manufacturing, storage, packaging, sale or distribution of drugs and/or medical device products.

Examples of Pharmaceutical Laws in a sentence

  • Except as provided under applicable law, including any applicable Health Care Laws, Pharmaceutical Laws and privacy laws, and except as would not be expected to result in a Material Adverse Effect, (i) there are no limitations or restrictions on the rights of any Grantor to sell, transfer or otherwise assign any Prescription List to any third party; and (ii) each Prescription List is in good and marketable condition.

  • The Company and each Subsidiary has, in all material respects, complied with all laws, regulations and orders applicable to their respective businesses, including Pharmaceutical Laws (as defined below), and have all material permits and licenses required thereby.

  • All such filings, declarations, listings, registrations, reports, applications or submissions were in material compliance with applicable Pharmaceutical Laws when filed and remain in full force and effect.

  • Each Loan Party will, and will cause each of the Subsidiaries to, comply with all Applicable Laws (including Pharmaceutical Laws, Health Care Laws and HIPPA), except where the failure to do so, individually or in the aggregate, could not reasonably be expected to result in a Material Adverse Effect.

  • Pharmaceutical Laws..................................................................................

  • The Borrower and its Subsidiaries have obtained all material permits, licenses and other authorizations which are required with respect to the ownership and operations of their businesses under all Pharmaceutical Laws.

  • The Company and each Subsidiary has, in all material respects, complied with all laws, regulations and orders applicable to its business, including Pharmaceutical Laws (as defined below), and has all material permits and licenses required thereby.

  • Except as set forth in Section 3(h) of the Disclosure Letter, the Company has, to the Company’s knowledge, in all material respects, complied with all laws, regulations and orders applicable to its business, including Pharmaceutical Laws (as defined below), and has all material permits and licenses required thereby.

  • In marketing, distributing, offering to sell or selling the LdT Drug Product, SUMITOMO will, and will make Commercially Reasonable Efforts to cause its Affiliates and any Permitted Sub-Distributors to comply with all applicable Pharmaceutical Laws, Laws (as hereinafter defined), and all other applicable laws, rules, regulations and guidelines generally accepted in the pharmaceutical industries in the Territory.

  • The Company has, in all material respects, complied with all laws, regulations and orders applicable to its business, including Pharmaceutical Laws (as defined below), and has all material permits and licenses required thereby.


More Definitions of Pharmaceutical Laws

Pharmaceutical Laws means, with respect to the United States, the United States Food, Drug and Cosmetic Act of 1938, as amended from time to time, and the regulations and guidelines promulgated thereunder, and with respect to any other governmental unit in the Territory (whether federal, state, municipal or other), the laws, regulations and guidelines of such governmental unit pertaining to pharmaceuticals, including the development, exportation, importation, use, manufacture, distribution, marketing and/or sale thereof.
Pharmaceutical Laws means federal (including, without limitation, the FFDCA), state and local laws, rules or regulations, codes, orders, decrees, judgments or injunctions issued, promulgated, approved or entered, relating to dispensing, storing or distributing prescription medicines or products, including laws, rules or regulations relating to the qualifications of Persons employed to do the same. Plan – an employee benefit plan now or hereafter maintained for employees of any Loan Party or any of their Subsidiaries that is covered by Title IV of ERISA.
Pharmaceutical Laws means the Pharmacy Act, 1991, the Drug and Pharmacies Regulation Act, 1990 the Regulated Health Professions Act, 1991 (each in force in the Province of Ontario from time to time) and the equivalent Laws or similar in other provinces or territories of Canada, the Controlled Drugs and Substances Act (Canada), the Food and Drugs Act (Canada), and the published rules, regulations, instruments and policies of any Governmental Authority administering those Laws, as well as all requirements, policies, directives, guidelines, guidance, principles, rulings, orders, decisions, interpretations, administrative views and codes and practices of any applicable Pharmaceutical Governing Body (whether in Ontario or otherwise) and the National Association of Pharmacy Regulatory Authorities and any applicable provincial or territorial pharmaceutical associations (whether in Ontario or otherwise).