Governance Quality Indicator The pharmacy reviews its own Standard Operating Procedures, and the Sample Clauses

Governance Quality Indicator The pharmacy reviews its own Standard Operating Procedures, and the referral pathways for the service, on an annual basis and whenever changes to the protocol are implemented. Community pharmacy providers will operate to appropriate standards of clinical governance as detailed in Essential Services 8 of the Community Pharmacy Contractual Framework (2005). In order to satisfactorily deliver this Enhanced Service as described in the Specification, pharmacy contractors will have a particular duty to ensure that: ▪ premises are of a standard suitable for such consultations ▪ usual steps are taken to maximise quality improvement and minimise risks involved in providing the service -which includes ensuring that ▪ there are demonstrably effective general policies, procedures and practice in place in relation to: • Health & Safety • Complaints • Confidentiality • Data ProtectionIncident ReportingInfection Control (Including Hand Hygiene) • Training, Development & Competence and also that ▪ pharmacists and staff involved in the provision of the stop smoking service (a) have relevant knowledge and are appropriately trained in the operation of the service and (b) are aware of and operate within the specific local operating protocols or procedures related to it. The Pharmacist Clinical Lead has overall responsibility for the safe and smooth running of the stop smoking service provided in their pharmacy. A Pharmacist Clinical Lead will normally be regularly employed to work in that pharmacy for at least 20 hours per week (35 - 40 hours in a 100 hour pharmacy). They will sign the SLA and have clinical responsibility for the operation of the service in that community pharmacy. Self assessment Describe how the governance criteria will be met and submit appropriate evidence • Provide copy of Standard Operating procedure • Infection control policies and associated SOPs Name of Pharmacist Clinical Lead Hours worked in pharmacy
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Related to Governance Quality Indicator The pharmacy reviews its own Standard Operating Procedures, and the

  • Quality Assurance/Quality Control Contractor shall establish and maintain a quality assurance/quality control program which shall include procedures for continuous control of all construction and comprehensive inspection and testing of all items of Work, including any Work performed by Subcontractors, so as to ensure complete conformance to the Contract with respect to materials, workmanship, construction, finish, functional performance, and identification. The program established by Contractor shall comply with any quality assurance/quality control requirements incorporated in the Contract.

  • Quality Assurance Program An employee shall be entitled to leave of absence without loss of earnings from her or his regularly scheduled working hours for the purpose of writing examinations required by the College of Nurses of Ontario arising out of the Quality Assurance Program.

  • Quality Control Program The Contractor shall describe the Quality Control Program in a written document which shall be reviewed by the Engineer prior to the start of any production, construction, or off-site fabrication. The written Quality Control Program shall be submitted to the Engineer for review at least ten (10) calendar days before the start of construction. The Quality Control Program shall be organized to address, as a minimum, the following items:

  • Drug and Alcohol Testing – Safety-Sensitive Functions A. Employees required to have a Commercial Driver’s License (CDL) are subject to pre-employment, post-accident, random and reasonable suspicion testing in accordance with the U.S. Department of Transportation rules, Coast Guard Regulations (46 CFR Part 16) or the Federal Omnibus Transportation Employee Testing Act of 1991. The testing will be conducted in accordance with current Employer policy.

  • Drug Testing Procedures a. The testing procedures and safeguards provided in this policy shall be adhered to by any laboratory personnel administering departmental drug tests.

  • Quality Management System Supplier hereby undertakes, warrants and confirms, and will ensue same for its subcontractors, to remain certified in accordance with ISO 9001 standard or equivalent. At any time during the term of this Agreement, the Supplier shall, if so instructed by ISR, provide evidence of such certifications. In any event, Supplier must notify ISR, in writing, in the event said certification is suspended and/or canceled and/or not continued.

  • Required Procurement Procedures for Obtaining Goods and Services The Grantee shall provide maximum open competition when procuring goods and services related to the grant-assisted project in accordance with Section 287.057, Florida Statutes.

  • Technical Standards Applicable to a Wind Generating Plant i. Low Voltage Ride-Through (LVRT) Capability A wind generating plant shall be able to remain online during voltage disturbances up to the time periods and associated voltage levels set forth in the standard below. The LVRT standard provides for a transition period standard and a post-transition period standard.

  • Use; Quality Control a. Neither party may alter the other party’s trademarks from the form provided and must comply with removal requests as to specific uses of its trademarks or logos.

  • NMHS Governance, Safety and Quality Requirements 3.1 Participates in the maintenance of a safe work environment.

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