Examples of Pharmaceutical Laws in a sentence
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.
Company employees with responsibilities in the areas governed by the FFDCA, FDA regulations and EU Pharmaceutical Laws are required to review, understand and comply with applicable laws and regulations.
This suggests that a more powerful means of support would therefore target such students with financial aid through bursaries, and more practical academic support throughout their time at university.
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.
Pharmaceutical Laws and Regulation are necessary because use of ineffective or poor quality drugs can result in therapeutic failure, worsening of disease condition, resistance development to drugs by microbes and even death resulting in undermining of the whole health sector.
Enact the necessary Pharmaceutical Laws and Regulations for the proper monitoring and control of the national pharmaceutical sector.
Cycle is committed to performing and conducting its business with integrity as demonstrated by compliance with federal, state, and other applicable laws, regulations, and guidance, including the Pharmaceutical Laws, Regulations, and Guidance discussed herein.
Adukiya, R., S., “Overview of Pharmaceutical Industry with Specific Reference to Pharmaceutical Laws of India”, PP., 1-97.
To Seller’s Knowledge, all preclinical and clinical investigations or trials sponsored by or conducted on behalf of Seller in connection with the Product have been conducted in material compliance with applicable Pharmaceutical Laws, including Good Clinical Practices requirements thereunder and Laws restricting the use and disclosure of individually identifiable health information.