You have accepted additional cookies. Reinstating Your License. M&A Pharmachem, a UK-based producer of complex molecules and OTC products, is recalling two batches of paracetamol 500mg tablets, each containing 12 pots of 1,000 tablets. You can also tell us about any factual errors that may have affected our decision. THANE ROAD, List of suspended licences for manufacturers and wholesalers of medicines updated, Updated the suspended list with two new suspensions and corrected suspension date for St Helen's Millennium Centre Services Limited. Updated 'Suspended manufacturing and wholesale distribution authorisations' attachment, Updated 'Suspended and revoked licences and registrations for manufacturers and wholesalers of medicines and ingredients', New Suspended manufacturing and wholesale distribution authorisations published, New list of suspended manufacturing and wholesale distribution authorisations, Addition of new revocation and suspension. A licence suspension is not a punishment: it is a temporary measure that gives us time to look into your case and/or await the outcome of investigations being carried out by the police or other public bodies. Dont include personal or financial information like your National Insurance number or credit card details. Following the end of the transition period, published information on new procedures for obtaining a marketing authorisation in the UK, Great Britain (England, Scotland and Wales) or Northern Ireland. Our legal power to do this is explained in Get Licensed (PDF, 3.03 MB, 90 pages). Download CSV If you respond to our letter we will take what you tell us into consideration. Visit the European Medicines Agency website for more information on the European requirements for cancellations or email the MHRA for UK requirements. Published updated 'Suspended manufacturing and wholesale distribution authorisations' spreadsheet. MHRA alerts & recalls PharmData maintains a list of all MHRA alerts and recalls relevant to community pharmacy. Use the pre-submission checklist (PDF, 129 KB, 7 pages) to help you with your application. Published a new version of the 'Get Licensed' document. The attorneys at The Davis Law Group, P.C. Do not send the corrected deficiencies by email. If we suspend your licence, the suspension comes into effect immediately. We publish the most up-to-date information for a medicine according to its licence history. Refusal of licence / variation or an existing licence being revoked. Any submission that does not meet the requirements will be rejected. CDL Disqualifications. The Medicines and Healthcare products Regulatory Agency (MHRA) may suspend a licence to wholesale or manufacture medicines and medical products if it: identifies safety issues needs to investigate a licence holder In certain circumstances MHRA will permanently revoke a licence. 09/02/2023. NOTTINGHAM, (MHRA) on safety, quality and efficacy of vaccines; MHRA responsible for Yellow Card Adverse Drug Reaction reporting system; Yellow Card reports can signal possibility that a product may be associated with certain risks. Converse Pharma could not be reached for comment. London, UK, 23 December 2021 Today Novartis announced that the Medicines and Healthcare products Regulatory Agency (MHRA) has approved the marketing authorisation to extend the licence in Great Britain for Piqray (alpelisib) for use in combination with fulvestrant for the treatment of postmenopausal women, and men, with hormone receptor Updated list of suspended licences added to the page. The information published in this Register was that held by the MHRA on the date of publication. . Download CSV UNITED KINGDOM, VIATRIS UK HEALTHCARE LIMITED, Dont include personal or financial information like your National Insurance number or credit card details. New document added to page for September 2017. We use some essential cookies to make this website work. The Medicines and Healthcare products Regulatory Agency (MHRA) first issued a partial suspension of the manufacturer's licence in August 2017, after it "identified non-compliance with good manufacturing practice" during an inspection of its Luton site in July.. Updated contact information for Department of Health for advice when seeking to fast-track an application due to a shortage of supply of essential medicines. Updated: list of suspended manufacturing and wholesale distribution authorisations, Updated: list of revoked manufacturing and wholesale distribution authorisations. Updated 'Medicines terminated, cancelled and revoked manufacturing and wholesale dealer licences'. We can suspend your licence for one or both of the following reasons: For example, we will suspend your licence if: Examples of what we mean by serious relevant offence are: terrorism, murder, manslaughter, rape, assault occasioning bodily harm (actual or grievous), battery, kidnapping, possession of indecent photographs of children, restriction of production and supply of controlled drugs. Updated both 'revoked' and 'Suspended' manufacturing and wholesale distribution authorisations lists. Post-license. Registered users can receive instant email notifications of new alerts, and record their responses to MHRA alerts within their PharmData account. A certificate of Good Manufacturing Practice (GMP) is issued to a manufacturer if the outcome of the inspection confirms that the manufacturer complies with the principles of Good Manufacturing Practice. If you want to fast track your application because of a shortage of supply we recommend you discuss this with DHSC by emailing DHSCmedicinesupplyteam@dhsc.gov.uk. Link to companies GMP and GDP certificates, see EUDRAGMDP link above. Full Service We develop, source and fill an extensive range of packaging types to suit product function, brand design and especially consumer driven needs, which we monitor with our non-stop trends service. You can change your cookie settings at any time. Added August file for - Medicines terminated, cancelled and revoked manufacturing and wholesale dealer licences. Updated list of suspended manufacturing and wholesale distribution authorisations added to the page. You will need to register if you havent already. List of new manufacturing licences and wholesale distribution authorisations 2015: https://www.gov.uk/government/publications/medicines-new-manufacturing-and-wholesale-dealer-licences, List of manufacturers licences MIA and MANA, MIA(IMP) on EUDRAGMDP link below: http://eudragmdp.ema.europa.eu/inspections/displayHome.do. The MHRA announces recall of paracetamol tablets, after certain products were found to be discoloured due to the presence of fungi. UK WDA (H) 12426. City sources said the company, which was formed from a management buyout in 2013, was in talks with its lenders at the state-backed NatWest Group and Secure Trust Bank about the process. Updated 'Suspended manufacturing and wholesale distribution authorisations' link. Copy CSV Excel PDF Print Showing 1 to 10 of 325 entries Previous 1 2 3 4 5 33 Next Updated 'Medicines terminated, cancelled and revoked manufacturing and wholesale dealer licences' link to latest January 2021 version. News stories, speeches, letters and notices, Reports, analysis and official statistics, Data, Freedom of Information releases and corporate reports. If you do not use this template your submission will be rejected. have helped thousands of drivers regain their driving privileges after cancellation, suspension or revocation. Removed link to Excel spreadsheet list of products. It can also be checked on the following register: You can print blog posts using the keyboard shortcuts "Control P" or "Command P". For example, in Kentucky, it takes an accumulation of 12 points over the course of 2 years in order to receive a suspension. Name and address of the site: NISA RETAIL LIMITED , BLOOM LANE, NORMANBY ENTERPRISE PARK, SCUNTHORPE, DN15 9YA, UNITED KINGDOM. D ate of . This is based on the MHRA assessment report with any commercially or personally confidential information removed. Also is there any process to verify that MIA licence is still valid? Dont worry we wont send you spam or share your email address with anyone. If you have submitted an application for a new MA, traditional herbal remedy and/or a parallel import product licence and you no longer want to proceed with application, you need to submit a withdrawal form. Uploaded new version of Suspended and revoked licences list. The use of POs is an internal control process and cannot be used as a reason to withhold payment of legitimate invoices. 94 RICKMANSWORTH ROAD, Healthcare products Regulatory Agency (MHRA) inspectorate as soon as possible. Updated list of suspended and revoked licences for manufacturers and wholesalers of medicines. You must do so within 21 days of the suspension coming into effect. The list of terminated and cancelled manufacturing and wholesale dealer licences has been updated. either alone or jointly. A drug distributor which had its licence suspended earlier this year by Britain's medicines watchdog has hired City advisers to raise tens of millions of pounds of new funding. LICENCE TYPE MA Manufacture and Assembly . Pay Restoration Fee Provide proof of payment of outstanding fines/tickets Parking Violations How to Pay Parking Tickets Added new list of terminated and cancelled manufacturing and wholesale dealer licences. New version of the revocation and suspension lists has been uploaded. The portal should be used for wholesale distribution authorisations [WDA(H)] and active substance manufacturers, importers and distributors new applications, variation applications and annual compliance reports (active substance manufacturers, importers or distributors only). 1 REDWOOD AVENUE, The Agency has the power to withdraw a product from the market, and in the case of medicines, to suspend production. All UK and Great Britain (England, Scotland and Wales) national applications should be submitted through the MHRA Submissions Portal. Actavis, Forley Generics, and Goldshield Group also . Maalox 175mg/200mg Oral Suspension . The Medicines and Healthcare products Regulatory Agency (MHRA) The MHRA looks at new drugs when pharmaceutical companies want to license medicines outside of the EMA's centralised authorisation procedure. News stories, speeches, letters and notices, Reports, analysis and official statistics, Data, Freedom of Information releases and corporate reports. Uploaded new Suspended manufacturing and wholesale distribution authorisations list. An example of when we might do this is if you are under police investigation for a serious offence. CB4 0GW, New version of document has been uploaded. https://www.gov.uk/government/publications/medicines-application-forms-for-a-manufacturer-licence, https://www.gov.uk/government/publications/medicines-variation-forms-for-a-manufacturer-licence, https://www.gov.uk/government/publications/mhra-fees, https://www.gov.uk/government/publications/medicines-new-manufacturing-and-wholesale-dealer-licences, http://eudragmdp.ema.europa.eu/inspections/displayHome.do, https://www.gov.uk/government/publications/human-and-veterinary-medicines-register-of-licensed-manufacturing-sites, https://www.gov.uk/government/publications/human-and-veterinary-medicines-register-of-licensed-wholesale-distribution-sites, https://www.gov.uk/government/publications/register-of-brokers-authorised-to-deal-in-human-medicines, https://www.gov.uk/government/publications/suspended-licences-for-manufacturers-and-wholesalers-of-medicines, https://www.gov.uk/export-a-human-medicine, https://www.gov.uk/government/publications/medicines-terminated-and-cancelled-manufacturing-and-wholesale-dealer-licences, Supply chain security: part 1 - introduction, Round Table: The impact of Electronic Health Records on UK Clinical Trials, Manufacture of Investigational Medicinal Products Frequently Asked Questions, MHRA Process for approving Manufacturing Authorisations or API Registrations in relation to unlicensed Cannabis-Based Products for Medicinal Use, Innovation, Quality & Transparency a Compliance Team 1 Perspective, licences for the manufacture/importation of licensed medicinal products for human use, commonly abbreviated to MIA, 'specials' licences for the manufacture/importation of unlicensed medicinal products for human use, commonly abbreviated to MS, authorisations for the manufacture/importation of investigational medicinal products for human use, commonly abbreviated to MIA(IMP), authorisations for the manufacture/importation of licensed medicinal products for veterinary use (ManA), 'specials' licences for the manufacture of unlicensed medicinal products for veterinary use, (ManSA), manufacturer's licences for exempt advanced therapy medicinal products (MeAT), licences for the wholesale distribution of medicinal products for human use, commonly abbreviated to WDA (H) (including those covering unlicensed medicines obtained from another EEA member state), licences for the wholesale distribution/importation of medicinal products for veterinary use - WDA (V), active substance manufacturer, importer or distributor registrations, certificates of Good Manufacturing Practice (GMP), certificates of Good Distribution Practice (GDP), new applications typically take 90 working days to process, variations where no inspection is required: 30 working days - variations where an inspection is required: 90 working days, new applications for registration as Active Substance manufacturers, importers and distributors take 60 working days - if an inspection is required: 90 working days. We updated the list of suspended manufacturing and wholesale distribution authorisations. Well send you a link to a feedback form. Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA. Updated the Suspended manufacturing and wholesale distribution authorisations list. Updated the Suspended manufacturing and wholesale distribution authorisations list, Added an updated version of the Suspended manufacturing and wholesale distribution authorisations list, Updated Suspended manufacturing and wholesale distribution authorisations csv file, New Suspended manufacturing and wholesale distribution authorisations list uploaded, Updated suspended manufacturing and wholesale distribution authorisations list, Suspended manufacturing and wholesale distribution authorisations updated to include HMS WHOLESALE LIMITED terminated licence, New Suspended manufacturing and wholesale distribution authorisations uploaded, New Suspended manufacturing and wholesale distribution authorisations updated. UNITED KINGDOM, WOODLEY BIOREG LIMITED, MILTON ROAD, Updated Suspended manufacturing and wholesale distribution authorisations CSV file. The list of terminated and cancelled manufacturing and wholesale dealer licences has been updated to include May 2015. You have rejected additional cookies. We look forward to hearing from you to discuss your case. UNITED KINGDOM, BCM LIMITED, If you use assistive technology (such as a screen reader) and need a The MHRA has been assured that acceptable standards of Good Manufacturing Practice are in place for . If the referral results in an immediate suspension of a manufacturer's/wholesale dealer's licence, there are no rights of appeal for the immediate suspension (which can last no longer than 3 months), but the suspension can be challenged in the High Court. It also covers 'sunset-clause' monitoring. We can maintain the suspension until we are in a position to make one of the following decisions: We will usually suspend your licence if you have been charged with a relevant offence. Or if you need to cancel a parallel import product. Updated 'Revoked manufacturing and wholesale distribution authorisations' and 'Suspended manufacturing and wholesale distribution authorisations' lists. Co-Amoxiclav DST Grunenthal 300/42.75mg Granules for Oral Suspension; Co-Amoxiclav DST Grunenthal 400/57mg Granules for Oral Suspension; Co-amoxiclav for Injection 1000/20mg; Co-amoxiclav for Injection 500/100mg; Co-Amoxiclav Injection 500/100; Co-Amoxiclav Oral Suspension 125mg/31.25mg/5ml Amoxi-Co 125/31

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