Life Science Graduates
Biology, chemistry, biomedical science, or pharmaceutical science graduates looking to launch a rewarding career in the pharma industry. No prior experience needed — just your degree and determination.
Complete Course Catalogue
13 courses covering every stage of your regulatory affairs career — from free introduction to advanced specialisation. All courses include real work experience.
Foundation Courses
Free
Free Regulatory Affairs Course
A 3-hour self-paced introduction to regulatory affairs. Includes a work experience assignment and case study so you can try regulatory work before committing.
- How to develop a regulatory strategy for an MAA
- What is in a Marketing Authorisation Application and the CTD
- How to classify an EU variation
- Drug development process and the role of RA
- Career paths, salaries, and how to get a job in RA
- Work experience assignment included
Most Popular
Free Live Webinar
How To Move Into Regulatory Affairs Without Experience — In 1 hour, discover exactly how to break into regulatory affairs with just a life science or healthcare degree.
- Learn what RA professionals really do and why it's in high demand
- Find out if your education is enough to start
- Why your applications are getting ignored and what recruiters want
- How to move into RA without years of "relevant experience"
- Real success stories: graduates securing RA roles in 2 weeks to 9 months
- The proven step-by-step roadmap to break into RA
- Common mistakes that keep talented candidates stuck
- Live career coaching and interactive Q&A
- Special gift at the end
Available Now
Core Regulatory Affairs Course
The same 50+ CPD hours and 3 months work experience as the Intro course, without career support services. Ideal if you prefer a self-directed job search.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- EU, US, and UK regulations
- Start anytime
- Expert ex-MHRA Professor Tutor
- Industry-recognised certificate
- Real-world case studies
Available Now
Comprehensive Regulatory Affairs Course
In-depth training for pharma, medical device, or RA professionals. Covers EU, US, and UK clinical trials, MAA, NDA, variations, and post-approval regulatory affairs with real work experience.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- EU, US, and UK regulations
- Job search mentoring until you get a job
- CV review, mock interview, careers hub
- Professional community access
- Industry-recognised certificate
Regional & Specialist Courses
July 2026
United States Regulatory Affairs Course
Focused US regulatory training covering FDA regulations, INDs, NDAs, post-approval changes, and regulatory strategy. Includes work experience in US-specific submissions.
- 40+ CPD hours of learning
- 3 months work experience (part-time)
- United States regulations focus
- Job search mentoring until you get a job
- CV review, mock interview, careers hub
- Expert Professor Tutor
- Industry-recognised certificate
July 2026
Europe & UK Regulatory Affairs Course
Focused EU and UK regulatory training covering EMA/MHRA procedures, MAAs, clinical trial applications, variations, and post-approval lifecycle management.
- 40+ CPD hours of learning
- 3 months work experience (part-time)
- Europe and UK regulations focus
- Job search mentoring until you get a job
- CV review, mock interview, careers hub
- Expert Former EMA/MHRA Professor Tutor
- Industry-recognised certificate
July 2026
Medical Device Regulatory Affairs Course
Specialist training for medical device regulation including EU MDR, US FDA pathways, UK MHRA approval procedures, UDI systems, EUDAMED, and conformity assessment.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- EU, US, and UK medical device regulations
- Job search mentoring until you get a job
- CV review, mock interview, careers hub
- Expert ex-Notified Body Tutor
- Industry-recognised certificate
September 2026
CMC — Small Molecules Regulatory Affairs Course
Deep-dive into CMC regulatory submissions for small molecule pharmaceuticals. Covers oral tablets, injectables, solutions/suspensions across generic, innovator, and sterile formulations.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- EU, US, and UK CMC regulations
- Formulations: oral tablets, injectables, solutions
- Submission types: generic, innovator, sterile
- Job search mentoring until you get a job
- Industry-recognised certificate
October 2026
CMC — Biologics Regulatory Affairs Course
Specialist CMC training for biologics including peptides, monoclonal antibodies, and antibody-drug conjugates. Covers innovator BLA, MAA, and biosimilar submissions.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- EU, US, and UK CMC regulations
- Biologics: peptides, mAbs, ADCs
- Submission types: BLA, MAA, biosimilars
- Job search mentoring until you get a job
- Industry-recognised certificate
November 2026
Global Regulatory Affairs Course (2 Regions)
Choose 2 regions for in-depth lectures and work experience. Regions include Canada, Middle East GCC, Australia, New Zealand, South Africa, Switzerland, Asia, and more.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- Choose 2 from 14+ global regions
- Start anytime
- Expert ex-MHRA Professor Tutor
- Industry-recognised certificate
November 2026
Global Regulatory Affairs Course (4 Regions)
Choose 4 regions for comprehensive global regulatory training with work experience in each. Master regulatory submissions across multiple markets simultaneously.
- 50+ CPD hours of learning
- 3 months work experience (part-time)
- Choose 4 from 14+ global regions
- Start anytime
- Expert ex-MHRA Professor Tutor
- Industry-recognised certificate
Career Support
Available Now
Regulatory Affairs Careers Support
Dedicated 1-to-1 career mentoring for anyone wanting to break into regulatory affairs or RA professionals needing job search support. Includes ongoing support until you secure a role.
- 1-to-1 mentoring through messages and calls
- Job search mentoring until you get a job
- Careers hub with training videos and resources
- Expert CV review
- Mock interview and interview resources
- Biweekly job search check-in calls
- Lifetime access to online careers hub
September 2026
Regulatory Affairs Work Experience — 1 to 12 Months
Flexible work experience placements for RA professionals wanting hands-on experience in new regulatory areas, regions, or submission types. Choose your duration and focus.
- 1 to 12 months flexible duration
- 14+ country/region options
- Clinical trials, NDA, MAA, or post-approval work
- 1 month: £995 | 2 months: £1,395 | 3 months: £1,995
Success Stories from Our Graduates
Real people, real career transformations. See how our students transitioned into regulatory affairs roles at top organisations.
★★★★★
"The course gave me a clear understanding of regulatory work. Within 4 months I moved from hospital pharmacy to a regulatory affairs role at the MHRA."
★★★★★
"Insightful and practical. The work experience component was invaluable — it gave me real submissions to discuss in interviews."
★★★★★
"A must for academia-to-regulatory transitions. I received 2 job offers and secured a position with a salary of CHF 90,000."
★★★★☆
"Valuable insights on CTA/NDA and post-approval changes. The career mentoring helped me transition from project management to a generics RA executive role."
★★★★★
"The course led to 3 interviews and 2 job offers. I transitioned from research to a regulatory role at the MHRA within 4 months."
★★★★★
"The CV review and career support were exceptional. I secured a role at GSK through the programme's guidance and networking."
★★★★★
"As a pharmacist, the course helped me transition into a regulatory affairs manager role. The CV review was transformative."
★★★★★
"As an undergraduate, this programme gave me the competitive edge I needed. I achieved a placement at GSK — something I never thought possible."
Watch Our Graduates Share Their Stories
Hear directly from professionals who transformed their careers through our programme.
2025 Student Ratings (average 4.6 out of 5)
3→8
Knowledge Increase (out of 10)
Knowledge Increase (out of 10)
9/10
Tutor Expertise
Tutor Expertise
9/10
Lecture Quality
Lecture Quality
9/10
CV Review Effectiveness
CV Review Effectiveness
Salary & Career Outcomes in Regulatory Affairs
Regulatory affairs is one of the highest-paying careers in the pharmaceutical industry, with strong demand across all major markets.
| Role Level | UK (£) | USA ($) | Europe (€) | Switzerland (CHF) |
|---|---|---|---|---|
| Associate | £50,000 | $100,000 | €60,000 | CHF 100,000 |
| Manager | £80,000 | $140,000 | €80,000 | CHF 140,000 |
| Director | £110,000+ | $250,000 | €110,000+ | CHF 200,000 |
| Executive / VP | £150,000+ | $350,000+ | €200,000+ | CHF 250,000+ |
Figures based on industry salary surveys. Actual salaries vary by company, location, and experience.
Career progression in regulatory affairs can take you from
£30,000 entry-level → £150,000+ executiveWith remote working, international opportunities, and high demand across the industry.
0.25%
Success rate applying without RA experience
10%
Success rate applying with RA experience
40×
More likely to get hired with our 3 months work experience
💰 Salary & ROI Calculator
Select your target country and experience level to see potential salary ranges and return on investment.
£35,000 — £50,000 per year
Potential ROI: Course cost recovered in < 2 months of salary
Estimated salary increase vs typical lab/pharmacy role: +£10,000 — £20,000/year
Your Learning Journey
A clear, structured pathway from complete beginner to employed regulatory affairs professional.
FREE Live Webinar
Attend the free 1-hour live session to understand what RA involves and whether it is right for you.
Free Course
Complete the 3-hour self-paced course to build foundational RA knowledge at no cost.
Full Training
Enrol in the course that matches your goals. Gain 50+ CPD hours, 3 months work experience, and expert mentoring.
Career Launch
With your new skills, experience, and career support, secure your RA role. Average: 2 weeks to 6 months.
Download the Course Brochure
Get a comprehensive overview of all courses, pricing, and outcomes in one PDF.
Download Course Brochure (PDF)Compare Our Most Popular Courses
Find the right course for your goals, budget, and experience level.
| Feature | Free Course | Free Live Webinar Most Popular | Medical Devices RA | CMC Regulatory Affairs |
|---|---|---|---|---|
| Price | £0 | £0 | £1,986 | £1,986 |
| Duration | 3 hours | 1 hour live | 50+ CPD hours (3 months) | 50+ CPD hours (3 months) |
| Level | Beginner | Beginner | Intermediate | Advanced |
| Prerequisites | None | Life science / healthcare degree | Life science / engineering degree | Pharmacy / chemistry degree |
| Certificate | — | — | ✓ Industry-recognised | ✓ Industry-recognised |
| Work Experience | 1 assignment | — | 3 months | 3 months |
| Job Search Mentoring | — | — | ✓ Until hired | ✓ Until hired |
| Key Outcomes | Understand RA basics, career paths, and MAA structure | Learn salary potential, why applications fail, how to break in without experience, get career coaching | EU MDR, FDA device pathways, UK MHRA, UDI & EUDAMED | CMC submissions for small molecules or biologics (oral, injectable, mAbs, ADCs) |
| Best For | Anyone curious about RA | Anyone exploring RA careers | Those targeting medical device industry | QC/QA/CMC specialists |
| Start Free | Register Now | Register Interest | Register Interest |
Free Regulatory Affairs Course
- Price
- £0 — Completely free
- Duration
- 3 hours self-paced
- Level
- Beginner — No prerequisites
- Certificate
- —
- Key Outcomes
- Understand RA basics, career paths, and MAA structure
- Best For
- Anyone curious about regulatory affairs
Most Popular
Free Live Webinar
- Price
- £0 — Completely free
- Duration
- 1 hour live session
- Level
- Beginner — Life science / healthcare degree preferred
- Schedule
- Every Thursday at 19:00 GMT
- Platform
- Online (Microsoft Teams)
- Key Outcomes
- Learn salary potential (up to £150k), why applications fail, how to break in without experience, get live career coaching
- Best For
- Anyone exploring regulatory affairs careers
Medical Device Regulatory Affairs
- Price
- £1,986
- Duration
- 50+ CPD hours over 3 months
- Level
- Intermediate — Life science / engineering degree
- Certificate
- ✓ Industry-recognised
- Key Outcomes
- EU MDR, FDA device pathways, UK MHRA, UDI & EUDAMED
- Best For
- Those targeting the medical device industry
CMC Regulatory Affairs
- Price
- £1,986
- Duration
- 50+ CPD hours over 3 months
- Level
- Advanced — Pharmacy / chemistry degree
- Certificate
- ✓ Industry-recognised
- Key Outcomes
- CMC submissions for small molecules or biologics
- Best For
- QC/QA/CMC specialists
Frequently Asked Questions
Approximately 6 hours per week. The course is designed for working professionals who want to study part-time without quitting their job. You can spread your study across evenings and weekends to fit your schedule.
No prior RA experience is required. You need a life science, healthcare, or pharmacy degree (or equivalent). 79% of our students start with zero RA experience. The course is specifically designed to take you from beginner to employable.
While we cannot guarantee employment, our Full Course includes job search mentoring that continues until you secure a role. Students typically find positions within 2 weeks to 9 months of starting. The combination of knowledge, real work experience, CV review, and mock interviews significantly improves your chances — our data shows experience holders are 40 times more likely to be hired.
We offer several flexible payment options: instalment plans to spread the cost, Klarna (buy now, pay later), and PayPal. Contact Rabiea to discuss the arrangement that works best for your situation.
All courses are delivered online and remotely. They include recorded lectures you can watch at your own pace, live sessions, real-world case studies, and practical work experience assignments. You join a cohort group and have access to materials for 3 months (with the option to upgrade to lifetime access via the course book).
Yes. All paid courses include an industry-recognised certificate valued by employers including the MHRA, GSK, and other top pharmaceutical firms. The certificate demonstrates your commitment to professional development in regulatory affairs.
Full Course students receive: expert tutor support throughout the programme, 1-to-1 mentoring via messages and calls, comprehensive CV review, mock interviews, access to the careers hub with training videos and resources, an exclusive professional community, and job search mentoring that continues until you are employed.
Unlike TOPRA, RAPS, or Udemy courses, our programme includes 3 months of real regulatory work experience — not just theory. You also receive expert CV review, interview preparation, EU/US/UK curriculum coverage, and ongoing career mentoring until you are employed. 20% of our students have already taken other RA courses and chose ours specifically for the practical experience component.
Absolutely. The course requires only 6 hours per week and is designed specifically for working professionals. Most of our students study alongside full-time jobs. Recorded lectures let you study at times that suit you, and the work experience assignments have flexible deadlines.
For most courses, you need a life science, healthcare, pharmacy, or engineering degree (or equivalent professional experience). The Free Course has no entry requirements — anyone interested in regulatory affairs can start today. Specific courses have additional prerequisites listed in their descriptions above.