Purpose of the Specification Sample Clauses

Purpose of the Specification. To ensure a consistent and equitable approach across England, a common national service specification must be used to govern the provision and monitoring of NHS Diabetic Eye Screening Programmes (NDESP). The purpose of the service specification for the NDESP is to outline the service and quality indicators expected by NHS England (NHSE) for NHS England’s responsible population. The NDESP was in a development phase during the implementation of the common pathway and that development is now complete. Local providers should now be delivering a service that meets the national service specification. Further developments of the service may commence during 2016/17 relating to the implementation of extended screening intervals. The national service specification reflects requirements for any early implementers of that potential development. The service specification is not designed to replicate, duplicate or supersede any relevant legislative provisions which may apply, e.g. the Health and Social Care Act 2008 or the work undertaken by the Care Quality Commission. The specification will be reviewed and amended in line with any new guidance as quickly as possible. This service specification needs to be read in conjunction with the current NDESP guidance and recommendations. These can be found on the NDESP website: NHS DESP Programme Standards: Guidance and updates on KPIs: xxxxx://xxx.xxx.xx/government/publications/young-person-and-adult- screening-submit-key-performance-indicator-data NDESP Operational Guidance: xxxxx://xxx.xxx.xx/government/collections/diabetic-eye-screening- commission-and-provide Guidance on Failsafe: NHS Screening Programmes Guidance, Managing Serious Incidents in the English NHS National Screening Programmes xxxxx://xxx.xxx.xx/government/publications/managing-safety-incidents-in- nhs-screening-programmes
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Purpose of the Specification. To ensure a consistent and equitable approach across England a common national service specification must be used to govern the provision and monitoring of Down’s, Xxxxxxx’ and Patau’s syndromes Screening (Trisomy 21, 18 &13) as part of the Fetal Anomaly Screening Programme (FASP). The purpose of the service specification is to outline the service and quality indicators expected by NHS England for the population for whom it is responsible and which meets the policies, recommendations and standards of the NHS Screening programmes. The service specification is not designed to replicate, duplicate or supersede any relevant legislative provisions which may apply, e.g. the Health and Social Care Act 2008 or the work undertaken by the Care Quality Commission. The specification will be reviewed and amended in line with any new guidance as quickly as possible. This specification should be read in conjunction with: • current FASP guidance xxxxx://xxx.xxx.xx/topic/population-screening- programmes/fetal-anomaly • FASP Ultrasound Practitioners Handbook xxxxx://xxx.xxx.xx/government/publications/fetal-anomaly- screening-ultrasound-practitioners-handbook • FASP Laboratory Handbook xxxxx://xxx.xxx.xx/government/publications/fetal- anomaly-screening-laboratory-handbook-xxxxx-xxxxxxx-and-pataus- syndromes • any separate service specifications for the screening laboratory used by the Provider for antenatal screening services • UK NSC Guidance, Managing Safety Incidents in the English NHS National Screening Programmes xxxxx://xxx.xxx.xx/government/publications/managing-safety-incidents-in- nhs-screening-programmes • Guidance & updates on Key Performance Indicators xxxxx://xxx.xxx.xx/government/collections/nhs-screening-programmes-national- data-reporting • Clinical Excellence (NICE) Clinical guideline 62 Antenatal care June 2010 xxxx://xxx.xxxx.xxx.xx/guidance/CG62 • National Institute for Health and Clinical Excellence (NICE) Clinical guideline CG 129 Antenatal care September 2011 • Royal College of Radiologists. xxxxx://xxx.xxx.xx.xx/publication/standards- provision-ultrasound-service • Service Specification Number 17 Fetal Anomaly Screening xxxxx://xxx.xxxxxxx.xxx.xx/commissioning/wp-content/uploads/sites/12/2016/02/serv- spec-17.pdf • ‘Maternity Pathway Payments: Who pays for what?-Aspects of the Maternity Pathway Payment for the Screening and Immunisations Programmes June 2015 xxxxx://xxx.xxxxxxx.xxx.xx/expo/wp- content/uploads/sites/18/2015/06/who-pays-mpp-upd-06-2015....
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Purpose of the Specification. To ensure a consistent and equitable approach across England a common national service specification must be used to govern the provision and monitoring of bowel scope screening. The purpose of the service specification is to outline the service and quality indicators expected by NHS England and NHS Improvement for the population for whom it is responsible, and which meets the policies, recommendations and standards of the NHS Bowel Cancer Screening Programme. This specification is not designed to replicate, duplicate or supersede any relevant legislative provisions which may apply, e.g. of the Health and Social Care Act 2008 or the work undertaken by the Care Quality Commission. The specification will be reviewed and amended in line with any new guidance as quickly as possible. This specification should be read in conjunction with the bowel scope screening guidance
Sample 1
Purpose of the Specification. To ensure a consistent and equitable approach across England a common national service specification must be used to govern the provision and monitoring of bowel cancer screening. The purpose of the service specification is to outline the service and quality indicators expected by NHS England and NHS Improvement for the population for whom it is responsible, and which meets the policies, recommendations and standards of the NHS Bowel Cancer Screening Programme. This specification is not designed to replicate, duplicate or supersede any relevant legislative provisions which may apply, e.g. of the Health and Social Care Act 2008 or the work undertaken by the Care Quality Commission. The specification will be reviewed and amended in line with any new guidance as quickly as possible. This specification should be read in conjunction with all NHS BCSP guidance
Sample 1
Purpose of the Specification. To ensure a consistent and equitable approach across England a common national service specification must be used to govern the provision and monitoring of fetal anomaly ultrasound screening services as part of the Fetal Anomaly Screening Programme (FASP). The purpose of the service specification is to outline the service and quality indicators expected by NHS England and NHS Improvement for the population for whom it is responsible and which meets the policies, recommendations and standards of the NHS Fetal anomaly screening programme. This specification is not designated to replicate, duplicate or supersede any relevant legislative provisions which may apply, e.g. of the Health and Social Care Act 2008 or the work undertaken by the Care Quality Commission. The specification will be reviewed and amended in line with any new guidance as quickly as possible. This specification should be read in conjunction with: • Service Specification Number 16 Fetal Anomaly Screening • FASP screening standards • Antenatal and newborn screening key performance indicators (KPIs) • FASP Ultrasound Practitioners Handbook • FASP Laboratory Handbook • FASP Screening Programme Handbook • Managing Safety Incidents in the English NHS National Screening Programmes • NHS England Serious Incident Framework • FASP Checks and audits to improve quality and reduce risks • National Institute for health and Clinical Excellence (NICE) Clinical guideline 62 Antenatal care • National Institute for Health and Clinical Excellence (NICE) Clinical guideline CG 129 Antenatal care for twin and triplet pregnancies • Royal College of Radiologists. Standards for provision of an ultrasound service. • Guidelines for the safe use of diagnostic ultrasound. British Medical Ultrasound Society The national screening team in Public Health England (PHE Screening) provides expert advice and support to the NHS Screening Programme. It does those things which make sense to do once rather than by each individual screening service. This includes: • developing and monitoring standards • producing public information leaflets • developing and commissioning training and education Providers should subscribe to the PHE Screening blog for the latest national news and updates. National documentation and guidance is published on XXX.XX.
Sample 1

Related to Purpose of the Specification

  • Escrow Format Specification Deposit’s Format. Registry objects, such as domains, contacts, name servers, registrars, etc. will be compiled into a file constructed as described in draft-xxxxx-xxxxxxx-registry-data-escrow, see Part A, Section 9, reference 1 of this Specification and draft-xxxxx-xxxxxxx-dnrd-objects-mapping, see Part A, Section 9, reference 2 of this Specification (collectively, the “DNDE Specification”). The DNDE Specification describes some elements as optional; Registry Operator will include those elements in the Deposits if they are available. If not already an RFC, Registry Operator will use the most recent draft version of the DNDE Specification available at the Effective Date. Registry Operator may at its election use newer versions of the DNDE Specification after the Effective Date. Once the DNDE Specification is published as an RFC, Registry Operator will implement that version of the DNDE Specification, no later than one hundred eighty (180) calendar days after. UTF-8 character encoding will be used.

  • Equipment Specifications All equipment must meet the contract specifications and all federal and State safety codes and regulations in effect at the date of manufacture. All equipment must be Original Equipment Manufacturer (OEM) equipment unless otherwise stated in the contract. All products, materials, supplies, replacement parts, and equipment offered and furnished must be new, of current manufacturer production, and must have been formally announced by the manufacturer as being commercially available, unless otherwise stated in this Contract.

  • DAF Specifications Developer shall submit initial specifications for the DAF, including System Protection Facilities, to Connecting Transmission Owner and NYISO at least one hundred eighty (180) Calendar Days prior to the Initial Synchronization Date; and final specifications for review and comment at least ninety (90) Calendar Days prior to the Initial Synchronization Date. Connecting Transmission Owner and NYISO shall review such specifications to ensure that the DAF are compatible with the technical specifications, operational control, and safety requirements of the Connecting Transmission Owner and NYISO and comment on such specifications within thirty (30) Calendar Days of Developer’s submission. All specifications provided hereunder shall be deemed to be Confidential Information.

  • Changes to Specifications All Specifications and any changes thereto agreed to by the parties from time to time shall be in writing, dated and signed by the parties. Any change to the Process shall be deemed a Specification change. No change in the Specifications shall be implemented by Catalent, whether requested by Client or requested or required by any Regulatory Authority, until the parties have agreed in writing to such change, the implementation date of such change, and any increase or decrease in costs, expenses or fees associated with such change (including any change to Unit Pricing). Catalent shall respond promptly to any request made by Client for a change in the Specifications, and both parties shall use commercially reasonable, good faith efforts to agree to the terms of such change in a timely manner. As soon as possible after a request is made for any change in Specifications, Catalent shall notify Client of the costs associated with such change and shall provide such supporting documentation as Client may reasonably require. Client shall pay all costs associated with such agreed upon changes. If there is a conflict between the terms of this Agreement and the terms of the Specifications, this Agreement shall control. Catalent reserves the right to postpone effecting changes to the Specifications until such time as the parties agree to and execute the required written amendment.

  • Service Specification The Parties have agreed upon the scope and specification of the Services provided under this Service Agreement in the Service Specification.

  • The Specifications The Specifications are that portion of the Contract Documents consisting of the written requirements for materials, equipment, systems, standards and workmanship for the Work, and performance of related services.

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