Medical Affairs Course Registration
Course registration closes on 25th November
Course Start date on 26th November
Few Spaces Left!
Ready To Kick Start Your Regulatory Career?
Here is How to Enrol and Pay for the
Medical Devices Regulatory Affairs Course
Choose the option that works for you
Pay in 1 Instalment - Lowest total price - Start when you like - global customers
Spread the cost with 3 Instalments - Start when you like - no credit check, 0% interest - £732 per month - global customers
Only £459 per month - Spread the cost with 5 Instalments - Start after 2 payments made - no credit check, 0% interest - globall customers
Salaire des affaires rรฉglementaires (2025)
United Kingdom
Associate - £51,000
Manager - £77,000
Director - £133,000
Executive - £194,000+
United States
Associate - $95,000
Manager - $150,000
Director - $280,000
Executive - $400,000
Europe
Associate - €62,000
Manager - €87,000
Director - €133,000
Executive - €204,000+
Switzerland
Associate - 100,000 CHF
Manager - 140,000 CHF
Director - 200,000 CHF
Executive - 252,000 CHF
Best Value
Medical Devices Course (Pay in 3)
732
Tous les mois
Pay ยฃ732 monthly, for three months
Valable pendant 3 mois
A minimum of 1 payment must be made before the course date
Best Value
Medical Devices Course (Pay in 5)
459
Tous les mois
Valable pendant 5 mois
A minimum of 2 payments must be made before the course date
Course Enrolment Options
If you would like to enrol onto the Full Comprehensive Regulatory Affairs Course,
you can pay over a period of 3 months or 5 months
Other Options
โHalf Course
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22+ CPD Hours of Learning
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EU, UK and US Regulations
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Expert ex MHRA Tutor
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Industry Recognised Certificate
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Real World Case Studies
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2 months Access - Additional charge for lifetime access - ~£100 Course Book
โCore Course
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50+ CPD Hours of Learning
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EU, UK and US Medical Device Regulations
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Expert ex-Notified Body and ex-MHRA Tutor
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Industry Recognised Certificate
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Real World Case Studies
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3 Months Work Experience (part-time)
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3 months online access
โFull Course
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3 Months Regulatory Affairs Work Experience / internship (with work reference)
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50+ CPD hours of Regulatory Lectures and Assignment (Includes FD&C, 21 CFR, 21 CFR 820, ISO 13485:2016, UDI, EUDAMED, MDR, IVDR)
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Careers Support Training and Resources – Full training, templates, and resources covering A to Z of your job search
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Expert Professor and ex-MHRA Tutor and ex-Notified Body Lecturer Tutor - Live support and Q and A sessions with expert
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Job Search Mentoring until you get a job – 1-1 mentoring, Live careers support**
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Industry Recognised Certificate
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Real World Case Studies
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1 x Expert CV Review
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1 x Mock Interview
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Exclusive Regulatory Community
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Additional Work Experience Project (additional charge)
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3 months online access - upgrade to lifetime Access available*
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European, United Kingdom and United States Regulations Covered
*Lifetime access to course book (additional charge)
**In the country where you have long-term right to work (where you have a valid sponsorship/visa already)
Comme vu dans :
Comme vu dans :
Comme vu dans :
En 40 jours, vous passerez d'une absence totale d'expรฉrience et de connaissances en matiรจre d'affaires rรฉglementaires ร :
โ Acquรฉrir plus de 40 heures de DPC de connaissances rรฉglementaires sur l'UE, les รtats-Unis et le Royaume-Uni
โ 4 semaines d'expรฉrience professionnelle en affaires rรฉglementaires
โ Mentorat en recherche d'emploi jusqu'ร ce que vous trouviez un emploi
โ Plusieurs entretiens
Le prochain cours complet commence le :
14 septembre
Seulement 15 places
Le cours se dรฉroule ร temps partiel sur un mois
Enregistrements ร la demande avec assistance en direct
In 3 months, you will progress from having no regulatory affairs experience and knowledge to:โ
โ
โ Gaining 50+ CPD hours of EU, US and UK regulatory knowledge
โ 3 months of regulatory affairs work experience
โ Job Search Mentoring until you find a job
โ Multiple interviewsโ
โ Past students have gained a regulatory affairs job on average, 2 weeks to 9 months from starting the course*
For other cohort dates email contact@entrytoregulatory.com
Your Current Case
Before the Course
You lose out on salaries of up to £51k (UK), $95k (US) or €62k (EU)
You keep getting rejected for regulatory roles. The chance of moving into regulatory affairs is 1 in 400 job applications
You spend months in an unfulfilling role with no career progression. You are in the same position after 1 year
You still have no regulatory submissions experience
You have no regulatory work reference
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You still have no or limited regulatory knowledge
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You do not have an industry-recognised regulatory certificate to help you break into pharma or regulatory
Best Case
After the Course
You move into a regulatory role within 2 weeks to 9 months of starting the course
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You get a salary of up to £51k (UK), $95k (US) or €62k (EU) - over 25x your course investment
You add 3 months of regulatory submissions experience to your CV
You get a professional work reference
โ
You get 50+ hours of regulatory knowledge
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You get an industry-recognised certificate
Worst Case
After the Course
You get monthly job search support calls until you find a job, careers support training and resources and mentoringโโ
You add 3 months of regulatory submissions experience to your CV and expand your career options
โ
You get a professional work reference for any job that you move into
โโ
You get 50+ hours of regulatory knowledge to expand your future career options
โโ
You get an industry-recognised certificate to help you break into pharma or regulatory now or in the future
โ
You join a supportive community of professionals looking to move into regulatory
Histoires de rรฉussite d'anciens รฉtudiants
De chercheuse postdoctorale ร stagiaire en affaires rรฉglementaires. Liviana Mummolo รฉtait chercheuse postdoctorale souhaitant percer dans l'industrie pharmaceutique. Mais elle n'avait aucune expรฉrience en pharmacie ni en affaires rรฉglementaires et ne savait pas par oรน commencer. Elle a suivi cette formation, oรน elle a acquis d'importantes connaissances rรฉglementaires. Son CV a รฉtรฉ รฉtudiรฉ et elle a obtenu plusieurs entretiens. Aprรจs son entretien blanc, elle a reรงu deux offres d'emploi. Elle a ensuite bรฉnรฉficiรฉ de conseils supplรฉmentaires pour choisir entre les offres. Elle travaille actuellement comme stagiaire en affaires rรฉglementaires pour une entreprise de dispositifs mรฉdicaux.
De prรฉparatrice en pharmacie ร responsable des affaires rรฉglementaires, Mme T.A. souhaitait changer de carriรจre. Diplรดmรฉe en sciences biomรฉdicales, elle รฉtait prรฉparatrice en pharmacie, mais son poste ne lui plaisait pas. Vivement intรฉressรฉe par une carriรจre dans les affaires rรฉglementaires, elle s'est lancรฉe dans cette formation. Aprรจs examen de son CV, elle a obtenu plusieurs entretiens et, grรขce ร une simulation d'entretien, s'est vu proposer un poste de chargรฉe des affaires rรฉglementaires pour une entreprise de dispositifs mรฉdicaux. Plus rรฉcemment, elle a รฉvoluรฉ vers un poste de responsable des affaires rรฉglementaires au sein de la mรชme entreprise.
De diplรดmรฉ en sciences pharmaceutiques ร un poste chez GSK. M. H. Malik รฉtait un jeune diplรดmรฉ en sciences pharmaceutiques avec seulement quelques mois d'expรฉrience en laboratoire. Il n'avait aucune expรฉrience prรฉalable en affaires pharmaceutiques ou rรฉglementaires, mais souhaitait percer dans l'industrie pharmaceutique. Aprรจs examen de son CV, il a reรงu une offre d'emploi de GSK en tant que coordinateur de projet, qu'il a acceptรฉe. Suite ร ce poste, il a รฉvoluรฉ vers l'assurance qualitรฉ, occupant plusieurs postes, dont celui de responsable AQ.
De sa licence en biochimie ร une offre de stage en affaires rรฉglementaires chez GSK. Mme S.A. รฉtait รฉtudiante en biochimie et aspirait ร devenir professionnelle en affaires rรฉglementaires. Avec une expรฉrience professionnelle limitรฉe, elle souhaitait obtenir un stage en affaires rรฉglementaires dans une entreprise pharmaceutique afin d'amรฉliorer ses perspectives de carriรจre. Cependant, les stages en affaires rรฉglementaires pour les รฉtudiants de licence sont trรจs compรฉtitifs. Pour se dรฉmarquer, elle a suivi cette formation en rรฉglementation et son CV a รฉtรฉ รฉtudiรฉ. Cela lui a permis d'obtenir une offre de stage en affaires rรฉglementaires chez GSK.
'I am very happy of course to finally transition from academia to...medtech... and so I really really recommend this course'
Liviana Mummolo
[Career Change]
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Past role: Postdoc Researcher
Role obtained: Regulatory Affairs Trainee (Medical
Devices)
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(Scientific Postdoc Researcher)
‘I can't recommend this enough. It is more than just a service; it is life changing. I had many interviews and got my first regulatory affairs job with a medical devices
company. Thank you’
Ms. T.A. [Career Change]
โ
Past role: Pharmacy Dispenser
Role obtained: Regulatory Affairs Officer (Medical
Devices), Regulatory Affairs Manager
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(Biomedical Sciences Degree)
‘This is truly exceptional when it came to obtaining a specific job I was pursuing. By the end, I was able to receive multiple job offers. I secured a job with GlaxoSmithKline!’
Mr. H Malik [Graduate]
Past role: Laboratory Scientist
Role obtained: Project Coordinator (GSK),
Quality Assurance Executive
(Pharmaceutical Science Degree)
‘I've gained a strong foundation in regulatory affairs, such as CTD structure, MAA change controls, variations and CMC, as well as undertaking work experience. I gained critical skills such as teamwork and effective communication’
Ms. S.A. [Undergraduate]
โ
Past role: Student
Role obtained: Regulatory Affairs placement offer from GSK
(Biochemistry Degree)
Histoires de rรฉussite d'anciens รฉtudiants
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Discounts for those:
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Unemployed for over 3 months
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In full-time education
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working for charities full-time
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NHS workers
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from low income countries (e.g. South Africa)
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Working in academia or government agencies.
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Multiple bookings (book with a friend or spouse)
Contact contact@entrytoregulatory.com to enquire about discount
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In-house training is available. Please contact contact@entrytoregulatory.com to enquire.
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If you are having any technical difficulties paying for the course, then please email contact@entrytoregulatory.com to request an invoice.
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Prices Converter
For prices in Dollars, Euros or any other currency, use the currency converter at the top of the page or click here
If you are from a low income country then request the discounted price from us before using the currency converter, contact contact@entrytoregulatory.com
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Note that the exact price is based on the conversion rate from UK Pounds at the time of ordering
*Usage of Klarna and Paypal (Pay in 3, Pay in 30 days) are subject to Klarna or Paypal terms and conditions and may not be available in all countries or to all persons.
Rapport de retour d'expรฉrience sur le cours 2025
8/10 means 8 points out of 10, where 10 out of 10 (10/10) is highly satisfactory and 0 out of 10 (0/10) is unsatisfactory.
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Overall Course Rating 4.6 stars out of 5 stars
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Regulatory affairs knowledge increased from 3/10 to 8/10 after the courseโ
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Likelihood of recommending the course was 8/10
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Quality and content of course book rated 8/10
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Knowledge of course tutor rated 9/10
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Confidence of applying for entry level regulatory role increased from 4/10 to 8/10 after the course
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Quality of lecture content rated 9/10
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Quality of case studies rated 9/10
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Quality of work assignments rated 9/10
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Satisfaction with quality of CV review 9/10
* Based on past students. However this is dependent on the effort you put into the course, work experience and job search process, as well as other factors. Success of past students are not a guarantee of your success. Your results will vary depending on region, education, effort, application, experience, and background. We cannot guarantee that you will be successful if you employ the advice specifically or generally. Consequently, your results may significantly vary from theirs. Specific experiences are mentioned for informational purposes only.
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