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My Lords, I say at once that I welcome certain aspects of the regulations we will debate tonight, specifically the help for social enterprises. However, I am concerned about their potential impact on the NHS, the enforced tendering of services that will entail and the potential confusion between two different...
My Lords, I say at once that I welcome certain aspects of the regulations we will debate tonight, specifically the help for social enterprises. However, I am concerned about their potential impact on the NHS, the enforced tendering of services that will entail and the potential confusion between two different...
My Lords, I am grateful to the noble Lord, Lord Hunt, for initiating this debate on what is a very important subject. Let me begin by emphasising one key point. The main purpose of the Public Contracts Regulations 2015 is to implement
the new EU procurement directive. There is no...
My Lords, I am grateful to the noble Lord, Lord Hunt, for initiating this debate on what is a very important subject. Let me begin by emphasising one key point. The main purpose of the Public Contracts Regulations 2015 is to implement
the new EU procurement directive. There is no...
My Lords, I thank the noble Earl for his response. He said that the imperative of the Government to introduce the regulations early is because of the economic benefits. Let me say at once that I have always accepted that there are some benefits in these regulations. I particularly welcome...
My Lords, I thank the noble Earl for his response. He said that the imperative of the Government to introduce the regulations early is because of the economic benefits. Let me say at once that I have always accepted that there are some benefits in these regulations. I particularly welcome...
Lords motion to regret that the Public Contracts Regulations 2015 laid before the House on 5 February are being implemented with unseemly haste, will cause confusion as to which procurement regime is to be used for integrated health and care contracts, and do not implement the assurances given by Ministers to Parliament during the passage of the Health and Social Care Act 2012 that NHS commissioners would be free to commission services in the way they consider in the best interests of NHS patients. (SI 2015/102). Motion withdrawn.
Lords motion to regret that the Public Contracts Regulations 2015 laid before the House on 5 February are being implemented with unseemly haste, will cause confusion as to which procurement regime is to be used for integrated health and care contracts, and do not implement the assurances given by Ministers...
My Lords, I am grateful to the noble Lord, Lord Hunt, for bringing this Motion. I will speak only very briefly because he has given most of the detail and said most of what I want to say, particularly about the confusion in the tendering and commissioning process. Integrating health...
My Lords, I am grateful to the noble Lord, Lord Hunt, for bringing this Motion. I will speak only very briefly because he has given most of the detail and said most of what I want to say, particularly about the confusion in the tendering and commissioning process. Integrating health...
To ask Her Majesty’s Government to what extent Council Directive 93/42 EEC of 14 June 1993 concerning medical devices and Directive 98/79 EEC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices applies to items such as IVF laboratory equipment or...
To ask Her Majesty’s Government to what extent Council Directive 93/42 EEC of 14 June 1993 concerning medical devices and Directive 98/79 EEC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices applies to items such as IVF laboratory equipment or...
The Human Fertilisation and Embryology Authority (HFEA) has informed us that it has been advised by the Medicines and Healthcare products Regulatory Agency (MHRA) that medical devices manufactured and used within the same healthcare institution without having been transferred to a different legal entity do not come within the scope of the Medical Devices Directives referred to, and do not therefore need to be CE marked.
I have nothing further to add to my previous answer of 20 February 2015, HL4711, regarding HFEA licencing conditions and guidance in relation to the use of CE marked and non-CE marked products.