Full Regulatory Compliance definition

Full Regulatory Compliance. - means compliance with all applicable permits for a facility such that the owner and/or operator of such facility will at all times maintain the ability to lawfully operate such facility or service without any interference with the service provided to CCCSWA, the Franchisees, Contractors, Permittees or constituents.

Examples of Full Regulatory Compliance in a sentence

  • Any Approved Processing Facility must have all permits from Federal, State, regional, County and city agencies necessary for it to operate as a Processing Facility and must be in Full Regulatory Compliance with all such permits and Applicable Law.

  • Contractor shall collect data and information, and maintain records and reports necessary to comply with this Agreement and maintain Full Regulatory Compliance.

  • Franchisee shall, directly or through similar obligations in its subcontract(s) with facility operators, keep all existing permits and approvals necessary for use of the Approved Processing Facility in Full Regulatory Compliance.

Related to Full Regulatory Compliance

  • Safety compliance facility means a licensee that is a commercial entity that receives marihuana from a marihuana facility or registered primary caregiver, tests it for contaminants and for tetrahydrocannabinol and other cannabinoids, returns the test results, and may return the marihuana to the marihuana facility.

  • FDA means the United States Food and Drug Administration or any successor agency thereto.

  • Accessibility Standards means accessibility standards and specifications for Texas agency and institution of higher education websites and EIR set forth in 1 TAC Chapter 206 and/or Chapter 213.

  • Regulatory Floodway means the channel of a river or other watercourse and the adjacent land areas that must be reserved in order to discharge the base flood without cumulatively increasing the water surface elevation more than a designated height.

  • Public Procurement Regulatory Authority (PPRA) means the Government Agency responsible for oversight of public procurement.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Subject of a Clinical Trial means the health care service, item, or drug that is being evaluated in the Approved Clinical Trial and that is not a Routine Patient Cost.