european medicines agency — Deutsch Übersetzung - TechDico Wörterbuch (2023)

EuropeanMedicinesAgency

p.m.

allgemein - eur-lex.europa.eu

A rare adverse reaction of sorafenib... The European Medicines Agency (EAMA) and Food and Drug Administration (FDA) approved the use of sorafenib in late-stage hepatic cellular cancer (HCC) on October 30, 2007, and November 19, 2007, respectively...

Stressregulation in der schwangerschaft und effekte auf die geburt... Die psy-chosoziale Stressbelastung des untersuchten Studienkollektivs von N = 405 Probandinnen im letzten Trimenon der Schwangerschaft (36,77 ± 1,89 SSW p...

Gesundheit / Tierisches Erzeugnis- core.ac.uk -PDF: doaj.orgEuropa / Zolltarifpolitik- core.ac.uk -PDF: archiv.ub.uni-heidelberg.de

Use of real-world evidence in postmarketing medicines regulation in the european union: a systematic assessment of european medicines agency referrals 2013-2017.OBJECTIVES:To assess the use, and evaluate the usefulness, of non-interventional studies and routinely collected healthcare data in postmarketing assessments conducted by the European Medicines Agency (EMA)...

Ungleichheit und heterogenität: die mehrebenenanalyse als instrument zur schätzung der effekte struktureller differenzierung... die aus der Sozialstruktur P...

Emcdda–europol joint report on a new psychoactive substance: n-phenyl-n-[1-(2-phenylethyl)piperidin-4-yl]cyclopropanecarboxamide (cyclopropylfentanyl).... The Joint Report was submitted to the Council, the Commission and the European Medicines Agency on 19 December 2017

Wirklichkeitsdarstellungen im kuba der 1960er jahreDie vorliegende Arbeit mit dem Titel „Wirklichkeitsdarstellungen im Kuba der 1960er Jahre – Eine Analyse der Filme Ciclón von Santiago Álvarez und P...

Regulatory issues: ema the europeanmedicines agency review of pertuzumab for the treatment of adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer: summary of the scientific assessment of the committee for medicinal... Pertuzumab x Perjeta x Breast cancer x EMA x European Medicines Agency Pertuzumab is a recombinant humanized monoclonal anti-body that specifically targets the extracellular dimerization domain (subdomain II) ofHER2...

Wieso achtsamkeitsmeditation vor depressionen schützen kann: erkenntnisse aus der hirnforschung..., Keune, P...

Russische und baltiache characterbilder aus geschichto und literatur....--P...

European Medicines Agency

EMA

Institutionen der Europäischen Union und Europäisc - iate.europa.eu

appointing four members of the Management Board of the European Medicines Agency (EMEA

zur Ernennung von vier Mitgliedern des Verwaltungsrats der Europäischen Arzneimittel-Agentur (EMA

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

appointing four members of the Management Board of the European Medicines Agency (EMA

zur Ernennung von vier Mitgliedern des Verwaltungsrats der Europäischen Arzneimittel-Agentur (EMA

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

An application for the establishment of MRLs for ciclesonide in equidae has been submitted to the European Medicines Agency (EMA').

Der Europäischen Arzneimittel-Agentur (im Folgenden EMA) liegt ein Antrag auf Festsetzung von Rückstandshöchstmengen für Ciclesonid bei Equiden vor.

Umweltschädigung -

eur-lex.europa.eu

on discharge in respect of the implementation of the budget of the European Medicines Agency (EMA) for the financial year 2017

über die Entlastung für die Ausführung des Haushaltsplans der Europäischen Arzneimittel-Agentur (EMA) für das Haushaltsjahr2017

Haushaltsplan -

eur-lex.europa.eu

An application for the establishment of MRLs for bambermycin in rabbit tissue has been submitted to the European Medicines Agency (EMA').

Der Europäischen Arzneimittel-Agentur (im Folgenden EMA) liegt ein Antrag auf Festsetzung von Rückstandshöchstmengen für Bambermycin in Gewebe von Kaninchen vor.

Tierisches Erzeugnis -

eur-lex.europa.eu

Interfaces of supercritical fluid chromatography with mass spectrometry and supercritical fluid extraction - applications in medicinal chemistry and bioanalysis

... Critical applications such as quantification of the newly approved antidepressant ketamine or the recently withdrawn analgesic flupirtine were comprehensively validated according to guidelines on bioanalytical method validation by the European Medicines Agency...

... Notably, this included the first fully validated chromatographic methods for the putative antidepressant (2R,6R)-6-hydroxynorketamine, and the first report of EMA-conforming quantification by on-line SFE-SFC-MS from urine...

Naturwissenschaften und angewandte Wissenschaften / Landwirtschaftliches Verarbeitungserzeugnis / Europa- core.ac.uk -

Best practice guide for clinical trials in accordance with the new european regulations and ich e6(r2)

The new European Clinical Trial Regulation 536/2014 will replace the Directive 2001/20/EC after the Clinical Tri...

...al Information System (CTIS) is published by the European Medicines Agency (EMA)...

Zolltarifpolitik- core.ac.uk -

European Medicines Agency

EMEA

Institutionen der Europäischen Union und Europäisc - iate.europa.eu

First amending budget of the European Medicines Agency (EMEA) for 2004

Erster Berichtigungshaushaltsplan der Europäischen Arzneimittel-Agentur (EMEA) für das Haushaltsjahr 2004

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

First amending budget of the European Medicines Agency (EMEA) for 2005

Erster Berichtigungshaushaltsplan der Europäischen Arzneimittel-Agentur (EMEA) für das Haushaltsjahr 2005

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

First amending budget of the European Medicines Agency (EMEA) for 2006

Erster Berichtigungshaushaltsplan der Europäischen Arzneimittel-Agentur (EMEA) für das Haushaltsjahr 2006

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

Second amending budget of the European Medicines Agency (EMEA) for 2004

Zweiter Berichtigungshaushaltsplan der Europäischen Arzneimittel-Agentur (EMEA) für das Haushaltsjahr 2004

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

First amending budget of the European Medicines Agency (EMEA) for 2007

Erster Berichtigungshaushaltsplan der Europäischen Arzneimittel-Agentur (EMEA) für das Haushaltsjahr 2007

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

Evaluation of the traditional and well-established use of hyperici herba

... The assessment of the literature was performed considering the guidelines of the EMEA (European Medicines Agency)...

... Der Bericht wurde nach den Richtlinien der EMEA (European Medicines Agency) erstellt...

allgemein- core.ac.uk -PDF: core.ac.uk

European Medicines Agency

Europäische Agentur für die Beurteilung von Arzneimitteln

Institutionen der Europäischen Union und Europäisc - iate.europa.eu

It may be necessary to review the MRLs set out in the Annex in the light of the results of a future evaluation of that active substance by the European Medicines Agency.

Es kann erforderlich sein, die im Anhang aufgeführten Rückstandshöchstmengen angesichts der Ergebnisse einer künftigen Bewertung dieses Wirkstoffs durch die Europäische Agentur für die Beurteilung von Arzneimitteln zu überprüfen.

Umweltschädigung -

eur-lex.europa.eu

European Medicines Agency

Europäische Arzneimittel-Agentur

Institutionen der Europäischen Union und Europäisc - iate.europa.eu

European Medicines Agency — Contribution to Title3

Europäische Arzneimittel-Agentur — Beitrag zu Titel3

allgemein -

eur-lex.europa.eu

European Medicines Agency — Contribution to Titles1 and2

Europäische Arzneimittel-Agentur — Beitrag zu den Titeln 1 und2

Umweltschädigung -

eur-lex.europa.eu

The European Medicines Agency has recommended three persons for nomination.

Die Europäische Arzneimittel-Agentur hat drei Sachverständige zur Ernennung vorgeschlagen.

Gesundheit -

eur-lex.europa.eu

The European Medicines Agency has recommended two persons for nomination.

Die Europäische Arzneimittel-Agentur hat zwei Sachverständige zur Ernennung vorgeschlagen.

Gesundheit -

eur-lex.europa.eu

The European Medicines Agency has recommended one person for nomination.

Die Europäische Arzneimittel-Agentur hat eine Person zur Ernennung vorgeschlagen.

Gesundheit -

eur-lex.europa.eu

Union contribution to the European Medicines Agency

17 03 12 01 Beitrag der Union zur Europäischen Arzneimittel-Agentur

allgemein -

eur-lex.europa.eu

The Director of the European Medicines Agency.

Der Direktor der Europäischen Arzneimittel-Agentur

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

THE MANAGEMENT BOARD OF THE EUROPEAN MEDICINES AGENCY

DER VERWALTUNGSRAT DER EUROPÄISCHEN ARZNEIMITTEL-AGENTUR

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

the European Medicines Agency and the European Centre for Disease Prevention and Control

die Europäische Arzneimittelagentur, das Europäische Zentrum für die Prävention und die Kontrolle von Krankheiten

the European Medicines Agency and the European Centre for Disease Prevention and Control

die Europäische Arzneimittelagentur, das Europäische Zentrum für die Prävention und die Kontrolle von Krankheiten

Gesundheit -

eur-lex.europa.eu

appointing a Commission representative to the Management Board of the European Medicines Agency

zur Ernennung eines Vertreters der Kommission im Verwaltungsrat der Europäischen Arzneimittel-Agentur

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

This Title shall not affect the competences vested in the European Medicines Agency.

Dieser Titel lässt die der Europäischen Arzneimittel-Agentur übertragenen Zuständigkeiten unberührt.

allgemein -

eur-lex.europa.eu

appointing a Commission representative to the Management Board of the European Medicines Agency

zur Ernennung eines Vertreters der Kommission im Verwaltungsrat der Europäischen Arzneimittel-Agentur

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

on closing the accounts of the European Medicines Agency for the financial year 2005

zum Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2005

Institutionen der Europäischen Union und Europäisc -

eur-lex.europa.eu

Approves closing the accounts of the European Medicines Agency for the financial year 2005

billigt den Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2005

Betriebliches Rechnungswesen -

eur-lex.europa.eu

Approves the closure of the accounts of the European Medicines Agency for the financial year 2012

billigt den Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2012

Betriebliches Rechnungswesen -

eur-lex.europa.eu

on the closure of the accounts of the European Medicines Agency for the financial year 2007

zum Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2007

Betriebliches Rechnungswesen -

eur-lex.europa.eu

on the closure of the accounts of the European Medicines Agency for the financial year 2009

zum Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2009

Betriebliches Rechnungswesen -

eur-lex.europa.eu

on the closure of the accounts of the European Medicines Agency for the financial year 2010

zum Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr

Betriebliches Rechnungswesen -

eur-lex.europa.eu

Approves the closure of the accounts of the European Medicines Agency for the financial year 2009

billigt den Rechnungsabschluss der Europäischen Arzneimittel-Agentur für das Haushaltsjahr 2009

FAQs

How long does it take to get EMA approval? ›

How long does it take? Upon submission of a valid application, the evaluation takes up to 210 days, at the end of which the Committee for Medicinal Products for Human Use (CHMP) must issue a scientific opinion on whether the medicine may be authorised or not.

How long is EMA review? ›

This first evaluation lasts up to 120 days.

How long does it take for a drug to be approved in Europe? ›

Following a positive recommendation from the Agency, the European Commission takes around two months to approve a medicine. The European Commission follows the opinion of the Agency in almost all cases.

What is the purpose of the European Medicines Agency? ›

The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA).

Will I still get EMA if I miss a day? ›

Your school decides if your EMA will be paid for each week. If your attendance isn't satisfactory, no payment will be made for that week unless your absence has been covered by a self-certification form or has been approved by your school. Make sure you keep your school updated on any absences.

What happens after EMA approval? ›

After approval, the product can be sold but not promoted until price is granted. Italy: L648 regulations allow sales prior to approval and after approval until price is granted. No sales or promotion is permitted apart from under L648 unless reimbursement granted.

How much is EMA per week? ›

EMA is a weekly payment of £30, paid every 2 weeks in arrears. If you qualify, you need to apply direct to your school or college. If you have any questions about how the EMA programme works, you can contact the Scottish Government EMA team. The EMA team cannot help with queries about your EMA application or award.

Does EMA get backdated? ›

Usually, if students submit their EMA application to the Student Loans Company before 30th September, they will have their weekly allowance payments backdated to the beginning of term.

What countries does EMA approval cover? ›

The EMA serves the EU and three countries from the EEA—Iceland, Norway, and Liechtenstein. The EMA practices pharmacovigilance to ensure the safety and efficacy of medicines.

How do I know if my drug is approved? ›

To find out if a drug is approved by FDA, consumers can use two different Internet sites:
  • Drugs@FDA lists most prescription and over-the-counter (OTC) drug products approved since 1939. ...
  • The FDA "Orange Book" contains drugs approved by FDA under New Drug Applications (NDAs) and Abbreviated New Drug Applications (ANDAs).
21 Sept 2017

What are the four stages of drug approval? ›

Typically, it can be divided into four main stages: Early Drug Discovery, Pre-Clinical Phase, Clinical Phases, and Regulatory Approval. Let's explore the major steps that are taken in each of these stages to develop a new drug.

What are the 4 types of procedures for approval of drug in EU? ›

Obtaining an EU marketing authorisation, step-by-step
  • Steps prior to submitting an application.
  • Submission of the application.
  • Assessment of the application.
  • European Commission decision on the marketing authorisation.
  • Voluntary sharing of market launch intentions: pilot project.

How many countries are in EMA? ›

The Board includes one representative of each of the 27 Member States, two representatives of the European Commission, two representatives of the European Parliament, two representatives of patients' organisations, one representative of doctors' organisations and one representative of veterinarians' organisations.

How many people work for the EMA? ›

EMA is a small professional company based in Saint Paul, MN with only 50 employees and an annual revenue of $890,000. To foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the european union (EU). Is This Your Company?

What is the role of the EMA in Europe Why was it established? ›

Founded in 1995, the European Medicines Agency (EMA) has worked across the European Union (EU) and globally to protect public and animal health by assessing medicines to rigorous scientific standards and by providing partners and stakeholders with independent, science-based information on medicines.

What income is taken into account for EMA? ›

EMA is paid fortnightly directly into the young person's bank account. The young person can spend the EMA on whatever they want. The annual income of the household in which the young person lives is the determinant of the level of the allowance.

Does lateness affect EMA? ›

After you are awarded an EMA

Payment of your EMA can be withheld if your school attendance falls below 100% in any one week. Lateness can also affect payments. If learning agreement conditions are not met, then your EMA may also be withheld.

What are the payment dates for EMA? ›

EMA payment dates
  • 12 July 2022.
  • 26 July 2022.
  • 9 August 2022.
  • 23 August 2022.
  • 6 September 2022.
  • 20 September 2022.
  • 4 October 2022.
  • 18 October 2022.

How long does it take for a drug to be approved in Germany? ›

The G-BA transfers the dossier to IQWiG , which uses these documents to conduct a comparison between the new and established drug. The entire process follows a strict timetable; the process must be completed after one year, or after 15 months at the latest.

How many drugs are approved by EMA? ›

Human medicines

In 2021, EMA recommended for authorisation: 92 new medicines. 53 new active substances.

What is EMA requirements? ›

You can only get EMA if you're on a non-advanced course (those studying up to and including Advanced Highers at school, college or through home education). If you're not sure if your course qualifies as non-advanced, you should speak to your learning provider.

How many hours is EMA? ›

you are full time at school or doing a minimum of 15 guided hours per week at college. you are studying an eligible course and attending all classes. you meet the nationality and residency rules set out in the EMA scheme.

Do you get bonus on EMA? ›

EMA comes in weekly payments of £30. If you live in Northern Ireland, on top of your weekly amount, you may also get bonuses if you continue to do well and meet targets set by your teacher when you start. You will only get your money if you regularly attend and work hard on your course.

Is EMA still being paid? ›

You may be able to claim Education Maintenance Allowance (EMA) if you're studying in Northern Ireland, Scotland or Wales. EMA is now closed in England. You can apply for: EMA in Northern Ireland.

When was EMA removed? ›

Scrapping in England

The United Kingdom Government under the Conservative/Liberal Democrat Coalition confirmed on 20 October 2010 that the Education Maintenance Allowance scheme in England was to be cancelled as part of a programme of budget cuts.

What is the difference between EU and EMA? ›

The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.

What is the difference between EU and FDA approval? ›

The FDA historically developed as a consumer protection agency, whereas the regulations from the European Commission arose out of a need to harmonize inter-state commercial interests while preserving national "autonomy." Thus, whereas the FDA has the advantages of centralization and common rules, the European Union ...

What is Europe's FDA called? ›

European Medicines Agency (EMA) : EMA is a decentralized body of the European Union, located in Amsterdam in the Netherlands. It is responsible for the scientific evaluation, supervision, and safety monitoring of medicines for human and veterinary use in the EU.

What is the process to get a drug approved? ›

FDA Drug-Approval Process. A pharmaceutical company seeking FDA approval to sell a new prescription drug must complete a five-step process: discovery/concept, preclinical research, clinical research, FDA review and FDA post-market safety monitoring.

Why does it take so long to get a drug approved? ›

Establishing a safety profile of a drug is a key reason why the process of drug development takes time. There are numerous studies that regulators require in determining if a drug is safe enough to be dosed in humans—and these safety studies continue throughout clinical trials and the drug's lifecycle.

How many times do you verify a medication? ›

The six rights of medication administration must be verified by the nurse at least three times before administering a medication to a patient.

What are the 5 stages of drug testing? ›

Information For
  • Step 1: Discovery and Development.
  • Step 2: Preclinical Research.
  • Step 3: Clinical Research.
  • Step 4: FDA Drug Review.
  • Step 5: FDA Post-Market Drug Safety Monitoring.
4 Jan 2018

What is a Phase 3 drug? ›

Phase III clinical trials compare the safety and effectiveness of the new treatment against the current standard treatment. Because doctors do not yet know which treatment is better, study participants are often picked at random (called randomized) to get either the standard treatment or the new treatment.

How long does a clinical trial take? ›

Clinical trials alone take six to seven years on average to complete. Before the potential therapy enters the clinical trial stage, researchers begin by investigating ideas in the discovery phase, which typically takes three to six years.

What are the 5 main categories of drug use? ›

7 Drug Categories
  • (1) Central Nervous System (CNS) Depressants. CNS depressants slow down the operations of the brain and the body. ...
  • (2) CNS Stimulants. ...
  • (3) Hallucinogens. ...
  • (4) Dissociative Anesthetics. ...
  • (5) Narcotic Analgesics. ...
  • (6) Inhalants. ...
  • (7) Cannabis.

What are the 3 categories of drug forms? ›

Drugs can be categorised by the way in which they affect our bodies: depressants – slow down the function of the central nervous system. hallucinogens – affect your senses and change the way you see, hear, taste, smell or feel things. stimulants – speed up the function of the central nervous system.

Who approves drug in Europe? ›

The EMA's Committee for Medicinal Products for Human Use (CHMP) conducts a scientific assessment of the application and gives a recommendation on whether the medicine should be authorized or not.

What are EU 15 countries? ›

Note : EU-15 area countries are: Austria, Belgium, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg, Netherlands, Portugal, Spain, Sweden and United Kingdom.

What countries are EU? ›

The EU countries are: Austria, Belgium, Bulgaria, Croatia, Republic of Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia, Slovenia, Spain and Sweden.

Who funds the European Medicines Agency? ›

Around 86% of the Agency's budget derives from fees and charges and 13% from the European Union (EU) contribution for public-health issues and less than 1% from other sources.

Who runs the EMA? ›

The European Medicines Agency's (EMA) Executive Director is Ms Emer Cooke.

Where are EMA headquarters? ›

The European Medicines Agency (EMA) building is located in the Zuidas district in south Amsterdam. The area is well connected by public transport and easily accessible from Schiphol Airport and Amsterdam Centraal station.

Is EMA like FDA? ›

Despite their differences, both the FDA and the EMA are geared toward a similar goal: the evaluation of the quality, safety and efficacy of medicinal products.

What is the EMA responsible for? ›

The EMA is mandated to write and enforce laws and regulations for environmental management, to educate the public about the nation's environmental issues and to control and prevent pollution, as well as conserve natural resources.

What is the importance of EMA? ›

EMAs are commonly used in conjunction with other indicators to confirm significant market moves and to gauge their validity. For traders who trade intraday and fast-moving markets, the EMA is more applicable. Quite often, traders use EMAs to determine a trading bias.

What are the role and functions of the EMA? ›

The Environmental Management Agency is a statutory body responsible for ensuring the sustainable management of natural resources and protection of the environment, the prevention of pollution and environmental degradation, the preparation of Environmental Plans for the management and protection of the environment.

How long do EMA results take Open University? ›

Getting your results

4.1 Results are usually available about six weeks after the exam period or EMA/emTMA submission date.

How do I know if I get EMA? ›

You can only get EMA if you're on a non-advanced course (those studying up to and including Advanced Highers at school, college or through home education). If you're not sure if your course qualifies as non-advanced, you should speak to your learning provider.

How far is EMA backdated? ›

Usually, if students submit their EMA application to the Student Loans Company before 30th September, they will have their weekly allowance payments backdated to the beginning of term.

How much EMA do you get a week? ›

EMA is a weekly payment of £30, paid every 2 weeks in arrears. If you qualify, you need to apply direct to your school or college. If you have any questions about how the EMA programme works, you can contact the Scottish Government EMA team. The EMA team cannot help with queries about your EMA application or award.

What happens if you fail your EMA Open University? ›

If this happens, you will normally receive a 'Fail: absent' module result and you would then have to retake the whole module in order to obtain credit.

What happens if you fail an ICMA? ›

Please note that ICMA will only cover the costs of one sitting of each exam. If you fail an exam on the first attempt, you may re-sit the exam at your own expense for an administration fee of EUR 50 per exam.

Is Open University degree valid? ›

Happily, many employers and organisations worldwide do employ Open University graduates and understand that an OU degree is equal in academic standard to a degree from any other British university.

How much do you have to earn for EMA? ›

In Wales, your family's income must be £23,077 or less. It also depends on how many dependant children there are in your household. You can find out about the scheme in Wales on the Education Maintenance Allowance (EMA) page of the Student Finance Wales website.

How often do you get EMA payments? ›

After signing your EMA Agreement, your school or college will confirm that you've been in attendance. As long as you meet the terms agreed with your school or college, you will get your payments every two weeks. Your EMA payments will be made directly into a bank account in your name.

Do you have to pay EMA back? ›

Yes – students will receive a back payment of any EMA support owed to them once the situation has been rectified. You should contact the school or college directly to ensure that they have provided the correct information to the EA to ensure reinstatement of payments and back payment.

Can I still claim EMA? ›

EMA applications for the academic year 2021 to 2022 have now closed. Application forms and notes, and general guidance information on the EMA Scheme for the academic year 2022 to 2023 are available to download using the link below.

Does getting a job affect EMA? ›

Yeah, what everyone else has said - EMA is done on your parents income, not yours, so your college doesn't need to know how much you're working.

When did EMA stop? ›

Scrapping in England

The United Kingdom Government under the Conservative/Liberal Democrat Coalition confirmed on 20 October 2010 that the Education Maintenance Allowance scheme in England was to be cancelled as part of a programme of budget cuts.

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