MBA with Professional Certificate in Drug Development Regulations

Tuesday, 17 February 2026 12:35:04

International Students can apply

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MBA with Professional Certificate in Drug Development Regulations

Overview

Drug Development Regulations


Mastering the complexities of regulatory frameworks is crucial for a successful career in the pharmaceutical industry.


Drug Development Regulations is an MBA with Professional Certificate program designed for professionals seeking to navigate the intricate world of regulatory compliance in drug development.

Learn from industry experts and gain a deep understanding of regulatory requirements, guidelines, and standards that govern the development, testing, and approval of pharmaceutical products.


Develop the skills and knowledge necessary to ensure compliance with regulatory bodies such as the FDA and EMA, and advance your career in this rapidly evolving field.


Take the first step towards a successful career in drug development by exploring this comprehensive program and discover how it can help you stay ahead of the curve.

Drug Development Regulations are a crucial aspect of the pharmaceutical industry, and our MBA with Professional Certificate in Drug Development Regulations program is designed to equip you with the necessary knowledge and skills to succeed in this field. By combining a Master's degree with a professional certificate, you'll gain a comprehensive understanding of the regulatory landscape, including drug development regulations, clinical trials, and pharmaceutical law. This program offers key benefits such as enhanced career prospects, improved job satisfaction, and increased earning potential. Upon completion, you'll be well-positioned to secure senior roles in the pharmaceutical industry, with opportunities in regulatory affairs, compliance, and more. (11)

Entry requirements

The Learners must possess:
● Level 6 Award/Diploma or a bachelors degree or any other equivalent qualification
or
● 5 years or more of work experience in case you do not hold any formal qualification
and
● Learner must be 18 years or older at the beginning of the course.


International Students can apply

Joining our world will be life-changing with a student body representing over 157 nationalities.

LSIB is truly an international institution with history of welcoming students from around the world. With us, you're not just a student, you're a member.

Course Content

•
• ICH E2 (R2) - International Conference on Harmonisation E2 (R2) - Good Clinical Practice •
• ICH E3 (R3) - International Conference on Harmonisation E3 (R3) - Good Laboratory Practice •
• ICH E4 (R4) - International Conference on Harmonisation E4 (R4) - Quality of Combined Post-Market Surveillance Reports •
• ICH E5 (R5) - International Conference on Harmonisation E5 (R5) - Clinical Requirements for Medicinal Products in the European Union •
• ICH E6 (R6) - International Conference on Harmonisation E6 (R6) - Guideline on Quality of Investigational New Drug Products •
• ICH E7 (R7) - International Conference on Harmonisation E7 (R7) - Guideline on Clinical Evaluation of Investigational Medicinal Products in the Context of Targeted Health Problems •
• ICH E8 (R8) - International Conference on Harmonisation E8 (R8) - Guideline on Pharmacovigilance •
• ICH E9 (R9) - International Conference on Harmonisation E9 (R9) - Guideline on The Investigation of Adverse Reactions •
• GCP (Good Clinical Practice)

Assessment

The evaluation process is conducted through the submission of assignments, and there are no written examinations involved.

Fee and Payment Plans

30 to 40% Cheaper than most Universities and Colleges

Duration

The programme is available in two duration modes:

12 Months: GBP £7700
18 Months: GBP £6700
This programme does not have any additional costs.
The fee is payable in monthly, quarterly, half yearly instalments.
You can avail 5% discount if you pay the full fee upfront in 1 instalment

Payment plans

12 Months - GBP £7700

● Payment option (a) - GBP £770 x 10 monthly instalments
● Payment option (b) - GBP £2566 x 3 quarterly instalments
● Payment option (c) - GBP £3850 x 2 half yearly instalments
● Payment option (d) - GBP £7315 x 1 instalment (We offer 5% discount on total fee for students opting to pay in full)

18 Months - GBP £6700

● Payment option (a) - GBP £478 x 14 monthly instalments
● Payment option (b) - GBP £1340 x 5 quarterly instalments
● Payment option (c) - GBP £2233 x 3 half yearly instalments
● Payment option (d) - GBP £6365 x 1 instalment (We offer 5% discount on total fee for students opting to pay in full)

40% Cheaper

Our course fee is upto 40% cheaper than most universities and colleges.

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Accreditation

 Stage 1 (Delivered by LSIB):
The programme involves delivery through on-line Learning Management System (LMS). This stage leads to award of Level 7 Diploma in Strategic Management and Leadership. Credits earned at this stage - 120 credits (60 ECTS).

Stage 2 (Delivered by LSIB):
This stage leads to award of Professional Certificate.

Stage 3 (Delivered by the University / awarding body)
On completion of the diploma programme you progress / Top up with Degree through a UK University for progression to the MBA degree. The stage 3 is delivered via distance learning by faculties from the University / awarding body. Credits earned at this stage - 60 credits (30 ECTS).

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  • 1. Complete the online enrolment form and Pay enrolment fee of GBP £10.
  • 2. Wait for our email with course start dates and fee payment plans. Your course starts once you pay the course fee.
  • Apply Now
    •

Got questions? Get in touch

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+44 75 2064 7455

admissions@lsib.co.uk

+44 (0) 20 3608 0144



Career path

Key facts about MBA with Professional Certificate in Drug Development Regulations

The MBA with Professional Certificate in Drug Development Regulations is a specialized postgraduate program designed for professionals in the pharmaceutical industry, regulatory affairs, and related fields.
This program focuses on the regulatory aspects of drug development, including compliance with international regulations, such as those set by the FDA, EMA, and ICH.
Through this program, learners will gain a deep understanding of the regulatory framework governing the development, approval, and commercialization of pharmaceutical products.
The learning outcomes of this program include the ability to analyze complex regulatory issues, develop effective regulatory strategies, and communicate with stakeholders in the pharmaceutical industry.
The duration of this program is typically 12-18 months, depending on the institution and the learner's prior experience.
The program is designed to be industry-relevant, with a focus on the latest trends and developments in regulatory affairs.
Learners will have the opportunity to develop skills in areas such as regulatory writing, compliance management, and risk assessment.
The MBA with Professional Certificate in Drug Development Regulations is a valuable asset for professionals looking to advance their careers in the pharmaceutical industry.
This program is particularly relevant for those working in regulatory affairs, compliance, and quality assurance, as well as for those looking to transition into these roles.
By completing this program, learners will be well-equipped to navigate the complex regulatory landscape of the pharmaceutical industry.
The program is delivered through a combination of online and on-campus learning, allowing learners to balance their studies with their work and other commitments.
Overall, the MBA with Professional Certificate in Drug Development Regulations is a comprehensive and industry-relevant program that provides learners with the skills and knowledge needed to succeed in the pharmaceutical industry.

Why this course?

The significance of an MBA with a Professional Certificate in Drug Development Regulations cannot be overstated in today's market. According to a recent survey by the Association of British Pharmaceutical Industry (ABPI), the UK pharmaceutical industry is expected to grow by 4.5% annually, with a projected value of £43.8 billion by 2025. This growth is driven by the increasing demand for innovative medicines and the need for effective regulatory frameworks to ensure their safe and efficient development.
Year Growth Rate
2020 3.5%
2021 4.2%
2022 4.5%
2023 4.8%
2024 5.1%
2025 4.5%

Who should enrol in MBA with Professional Certificate in Drug Development Regulations?

Ideal Audience for MBA with Professional Certificate in Drug Development Regulations Professionals in the pharmaceutical industry, particularly those in regulatory affairs, compliance, and quality assurance, are the primary target audience for this program.
Key Characteristics: Typically hold a bachelor's degree in a life science or related field, with 2-5 years of experience in the pharmaceutical industry, and a strong understanding of regulatory frameworks, such as the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK.
Career Goals: Upon completion of the program, graduates can expect to secure senior roles in regulatory affairs, compliance, or quality assurance, with average salaries ranging from £60,000 to £90,000 per annum in the UK.
Geographic Location: The program is designed to cater to professionals working in the pharmaceutical industry across the UK, with a focus on London and other major cities.