Gain regulatory affairs knowledge, work experience and
job mentoring to land your dream role
(no previous experience needed)
In 3 months, you will progress from having
no regulatory affairs experience and knowledge to:
✅ Gaining 50+ CPD hours of EU, US and UK regulatory knowledge
✅ 3 months of regulatory affairs work experience
✅ Job Search Mentoring until you find a job
✅ Multiple interviews
✅ Past students have gained a regulatory affairs job on average, 2 weeks to 6 months from starting the course*
Next Full Course Starts on:
14th June 2026
(April cohort sold out)
Limited Spaces Left
The course is held part time over 3 months (6 hours per week)
It is remote and online so you can take part from anywhere in the world
On-Demand Recordings with Live Support
Associate - £50,000
Manager - £80,000
Director - £110,000
Executive - £150,000+
Associate - $100,000
Manager - $140,000
Director - $250,000
Executive - $350,000
Associate - €60,000
Manager - €80,000
Director - €110,000
Executive - €200,000+
Associate - 100,000 CHF
Manager - 140,000 CHF
Director - 200,000 CHF
Executive - 250,000 CHF
Are you applying for numerous regulatory affairs jobs but are getting no interviews?
Did you know that most entry level regulatory affairs jobs require regulatory affairs experience?
But how do you gain work experience without your first chance?
We provide a two months regulatory affairs internship, with no previous experience needed, just a life science or healthcare degree.
Read on to learn more.
Got regulatory affairs experience already?
Excel in your career by gaining experience in European, UK and United States clinical trial, marketing authorisation application and variation submissions. Read on to learn more.
Liviana Mummolo was a postdoc researcher looking to break into the pharmaceutical industry. But she had no pharma or regulatory affairs experience and didn’t know where to start. She embarked on this course, where she gained significant regulatory knowledge. Her CV was reviewed and she gained multiple interviews. After her mock interview, she received two job offers. She then received further advice on how to choose between offers. She is now working as a regulatory affairs trainee for a medical devices company.
Ms. T.A. wanted a career change. She was a pharmacy dispenser with a Biomedical Science degree but was unfulfilled in her role. With a keen interest in pursuing a career in regulatory affairs, she embarked on the course. After her CV was reviewed, she gained multiple interviews and with the support of a mock interview, was offered a Regulatory Affairs Officer position for a Medical Devices company. More recently, she has progressed to a Regulatory Affairs Manager position within the same company.
Mr. H Malik was a recent pharmaceutical science graduate with only several months of laboratory experience. He had no previous pharmaceutical or regulatory affairs experience but wanted to break into the pharmaceutical industry. After his CV was reviewed, he received an entry level job offer from GSK as a Project Coordinator, which he accepted. Following this position, he moved into quality assurance, holding several positions, including as a QA executive.
Ms. S.A. was a Biochemistry undergraduate and aspiring regulatory affairs professional. With limited work experience, she wanted to gain a regulatory affairs placement in a pharmaceutical company to improve her career options. However, regulatory affairs placements for undergraduates are highly competitive. To stand out from the crowd she undertook this regulatory training and her CV was reviewed. This enabled her to obtain a Regulatory Affairs placement offer from GSK.
Overall Course Feedback
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.
“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]
Past role: Postdoc Researcher
Role obtained: Regulatory Affairs Trainee (Medical Devices)
(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]
Past role: Pharmacy Dispenser
Role obtained: Regulatory Affairs Officer (Medical Devices), Regulatory Affairs Manager
(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]
Past role: Student
Role obtained: Regulatory Affairs placement offer from GSK
(Biochemistry Degree)
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DOWNLOAD COURSE BROCHURESpeak to our expert about your career goals and any questions regarding the course.
We look forward to hearing from you.
Or send us an email
Want to get free access to several lectures, a case study and work assignment?
Associate Professor (Hon), UCL
Former MHRA Agency Reviewer
Managing Director
Advance Regulatory Consulting
Entry to Regulatory
I am an Honorary Associate Professor at UCL, a former MHRA Agency Reviewer and Managing Director of a regulatory affairs consultancy and regulatory affairs training company.
I have over ten years of regulatory affairs experience gained from working for the UK Regulatory Health Authority (MHRA) as an Agency Reviewer and several global pharmaceutical companies, such as, GSK, MSD and Bayer.
My experience covers the entire product lifecycle, from clinical trial applications through to new drug applications and post-approval changes. I have worked on various medicinal products, including cell and gene therapeutics, biologicals, vaccines, medical device combinations, consumer products (OTC), small molecule and generic medicinal products.
I have successfully delivered multimillion-dollar regulatory approvals and cost savings repeatedly for numerous pharmaceutical companies throughout the EU, US, UK, and rest of world markets.
I am passionate about regulatory affairs and providing exceptional regulatory support for pharmaceutical and biotechnology companies to accelerate innovation and deliver for patients. Furthermore, I am passionate about training other regulatory affairs professionals and growing the profession.
Follow me on LinkedIn
A profession responsible for the licensing and compliance of medicines to government regulatory standards through submissions to agencies that demonstrate the quality, safety and efficacy of a medicine.
Regulatory affairs professionals are responsible for keeping up to date with legislation and guidelines, ensuring medicines comply with regulatory requirements, authoring and preparing regulatory submissions throughout the lifecycle of a medicine, creating regulatory strategies and managing projects.
We conducted a study to find out why
For an entry level regulatory affairs role, there were 400 applicants
Which applicants would you interview?
Where do you fit in this ranking?
What do you need to do to increase your chances?
Recruiters will only consider those with regulatory experience
❌ No regulatory affairs work experience
400 job applications
(0.25% success rate)
✅ Regulatory affairs work experience
10 job applications
(10% success rate)
Gain regulatory affairs knowledge, work experience
and job mentoring to land your dream role
Are you looking for an entry level role in regulatory affairs?
Gain work experience in regulatory affairs even if you are new to this field.
If you are interested in becoming a regulatory affairs professional but have no experience, or if you are working in regulatory affairs but would like to expand your regulatory affairs knowledge, then this course is for you.
This is the most comprehensive regulatory affairs introductory course available, which includes:
Starting a course can be challenging. However, this course was made for those who are working full time. You only need to spend 6 hours per week on the course. Here is an example of how to plan your learning:
For each week, structure your learning as follows:
| Monday | Tuesday | Wednesday | Thursday | Friday | Saturday | Sunday |
|---|---|---|---|---|---|---|
| Rest | Rest | 1.5 hours | 1.5 hours | 1.5 hours | 1.5 hours | Rest |
1.5 hours of lectures or work assignment each day
(part-time online course)
Module 1 Variations Work Assignment
Module 1 Lectures and Case Studies
Welcome and Course Overview
Drug Development and What is Regulatory Affairs?
What is the Role of the Regulatory Affairs Professional?
Background of Medicines Legislation - US, EU, UK
EU and UK Regulatory Procedures Part 1
EU and UK Regulatory Procedures Part 2
US regulatory procedures, clinical trials, MAA, NDA, and variations
Clinical regulatory affairs, medical devices, pharmacovigilance, and eCTD Modules 1-5
Labelling, regulatory strategy, agency questions, and scientific advice
CV review, mock interview, careers hub, and recruiter strategies
| Half Course | Core Course | Full Course | |
|---|---|---|---|
| 11+ CPD Hours of Learning | ✅ | ||
| 50+ CPD hours of learning | ✅ | ✅ | |
| EU, UK and US Regulations | ✅ | ✅ | ✅ |
| Expert ex MHRA Tutor | ✅ | ✅ | ✅ |
| Industry Recognised Certificate | ✅ | ✅ | ✅ |
| Real World Case Studies | ✅ | ✅ | ✅ |
| Work Experience (3 months, part time) | ✅ | ✅ | |
| Lifetime access (Course Book) | ✅ | ||
| 3 month online access. Lifetime access if course book added | ✅ | ||
| Additional Work Experience available** | ✅ | ||
| Job Search Mentoring (until you get a job)* | ✅ | ||
| Careers Hub Training Resources | ✅ | ||
| Expert CV Review | ✅ | ||
| Mock Interview | ✅ | ||
| Exclusive Professional Community | ✅ |
*In the country where you have long term right to work (where you have a valid sponsorship/visa already)
** Subject to additional charge
| Feature | Entry to Regulatory | Others |
|---|---|---|
| Comprehensive lecture series | ✅ | ✅ |
| Expert teacher | ✅ | ✅ |
| Case studies | ✅ | ✅ |
| Certificate | ✅ | ✅ |
| Professional reference | ✅ | ❌ |
| Work experience | ✅ | ❌ |
| Job search mentoring & resources | ✅ | ❌ |
| 40+ CPD hours of learning | ✅ | ❌ |
| Expert CV review | ✅ | ❌ |
| Mock interview | ✅ | ❌ |
| EU, US and UK Regulations | ✅ | ❌ |
| Exclusive Community | ✅ | ❌ |
| Remote and part-time | ✅ | ❌ |
| Recorded lectures with live support | ✅ | ❌ |
Want to get free access to three lectures, a case study and work assignment?
Please click here for the course fees
This course is designed for those who are working/studying and short of time. The lectures are recorded and the work assignments can be done from home. You spend a total of 6-hours per week on the training. You choose when to spend those 6-hours as long as you meet the submission deadlines.
This course is an industry recognised qualification with the primary aim of providing you with in-depth regulatory affairs knowledge and experience to assist you in getting a regulatory affairs job. So far it has been recognised by the MHRA, large pharma companies, medical device companies, small biotechs and regulatory consultancies.
CV review, mock interview, job search mentoring until you get a job, exclusive community access and job search advice and resources.
Please click here for contact options.
Yes. There are modules directly applicable to other countries, such as eCTD content. There are topics that are indirectly applicable. These topics are still relevant as other countries align their regulations to the EU or US and submissions are made to the EU or US first and then updated slightly for other countries. We welcome students across the world, including those from the UK, USA, Canada, Europe, Switzerland, UAE, Saudi Arabia and South Africa who have or are studying for a life science/healthcare degree or higher qualification. No previous experience is needed.
* 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.
Join hundreds of professionals who have launched their regulatory affairs careers with Entry to Regulatory
