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Residents of village street claim they have been living with 'horrendous' rat infestations for years

Residents of village street claim they have been living with horrendous rat infestations for years
WARNING: This article contains an image of a dead animal which some may find distressing
16:20, 20 APR 2021
Neath Port Talbot has seen a 17% increase in calls about rats and mice since the start of the pandemic.
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Orphan medicinal products in Great Britain

Orphan medicinal products
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
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The MHRA offers incentives in the form of market exclusivity and full or partial refunds for marketing authorisation fees to encourage the development of medicines in rare diseases. Waiver from scientific advice fees will also be available for UK based
SMEs.
Application process
The MHRA is responsible for reviewing applications from companies for orphan designation at the time of a marketing authorisation application (
MAA).
There is no pre-marketing authorisation orphan designation.
Products with an orphan designation in the EU can be considered for a Great Britain orphan marketing authorisation (MA). In accordance with Regulation 50G of the Human Medicines Regulation 2012 (as amended), a UK-wide orphan marketing authorisation can only be cons ....

United Kingdom , Great Britain , Commission On Human Medicines , United Kingdom Licensing Authority , Customer Services Centre , United Kingdom Rare , Authorisation Applicants , Human Medicines , Marketing Authorisation , Products Characteristics , Trade Association , ஒன்றுபட்டது கிஂக்டம் , நன்று பிரிட்டன் , தரகு ஆன் மனிதன் மருந்துகள் , ஒன்றுபட்டது கிஂக்டம் உரிமம் அதிகாரம் , வாடிக்கையாளர் சேவைகள் மையம் , ஒன்றுபட்டது கிஂக்டம் ரேர் , மனிதன் மருந்துகள் , ப்ராடக்ட்ஸ் பண்புகள் , வர்த்தகம் சங்கம் ,

Register to make submissions to the MHRA

Register to make submissions to the MHRA
Submissions related to human medicines need to be submitted directly to the MHRA.
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For applications that you plan to submit to the UK (for example, a Marketing Authorisation for the UK or GB market), you will need to submit the information through our national portals. For those regulatory submissions made through European procedures you will need to continue to submit via the EU portals (for example, CESP).
The information on how to make submissions to the MHRA is for the following groups:
all pharmaceutical companies involved in making medicines regulatory submissions and vigilance activities for UK/GB licences ....

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