Top 10 Regulatory Affairs Training Institutes in Pune — 2024

Jaydeep Deva
8 min readApr 25, 2024

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The life sciences industry in India is experiencing tremendous growth, leading to a surge in demand for qualified regulatory affairs professionals. These specialists are crucial in ensuring drugs, medical devices, and other healthcare products adhere to stringent government regulations for safety, efficacy, and quality.

Are you a life science graduate interested in a career within this dynamic field? Consider pursuing training at one of Pune’s many well-respected institutes offering programs in regulatory affairs. Here’s a closer look at some of the top options:

1. TechnoBridge Systems Pvt Ltd — Regulatory Affairs Course with Placement

TechnoBridge Systems Pune Contact No.: +91 9257035703

TechnoBridge Systems offers a Regulatory Affairs Course in Pune designed for individuals seeking careers in the pharmaceutical or medical device industry. This intensive 3-month program is led by instructors with over 27 years of experience and equips you with the essential knowledge for a successful career in Regulatory Affairs. With a focus on practical application and industry needs, TechnoBridge boasts a 100% placement assistance program to help graduates secure their dream jobs in Regulatory Affairs. TechnoBridge have a dedicated placement team to provide placement call to every candidate until they secure placement.

Course: Post Graduate Diploma in Regulatory Affairs (PGDRA).

Duration: 3 months.

Fees: 27000–32000/-.

Training Mode: TechnoBridge offers flexible training options, online learning modules, and practical case studies. Online Regulatory Affairs Course

Why TechnoBridge Systems for Regulatory Affairs Course in Pune? Key features

  • Industry-relevant curriculum
  • 100% Placement Assistance with reputed companies.
  • Flexible learning options to suit your needs.
  • Experienced and qualified faculty.
  • Best and Affordable Price
  • 95% Placement Record
  • Unlimited Placement Calls
  • Best and Affordable Price
  • Interview Preparation
  • Certification Provided
  • Complete Job Support

Get Free Career Guidance Here +91 9257035703

Regulatory Affairs Course Syllabus by TechnoBridge [Updated 2024]

· Module:1- Introduction to Clinical Research

· Module:2- Good Clinical Practice (GCP)-ICH E6

· Module:3- Drug Development Process

· Module:4- Introduction to RA and Regulatory Bodies

· Module:5- Design of Trials

· Module:6- Regulatory Affairs

· Module:7- Privacy and Confidentiality

· Module:8- Application, Approval and Quality Assurance in RA

Other Courses Provided by TechnoBridge Systems:

· Pharmacovigilance Course

· Clinical Research Course

· Clinical Data Management Course

· Regulatory Affairs Course

· Medical Coding Course

· Medical Writing Course

Check TechnoBridge Student Reviews:

YOGESH BAHADUR

*****

I recently completed the regulatory affairs course offered by TechnoBridge Systems, and I am thoroughly impressed. The course content was comprehensive, up-to-date, and aligned with industry standards. The instructors were highly experienced professionals who imparted their expertise with great enthusiasm. The online learning platform was intuitive and interactive, there is also live doubt clearing sessions on weekends. TechnoBridge Systems truly exceeded my expectations, and I highly recommend their regulatory affairs program to anyone looking for quality education.

rushi petkar

*****

The mentor of Regulatory Affairs Course is highly experienced and passionate about teaching. I felt motivated and inspired throughout the course.

Samiksha Deshmukh

*****

It’s very cooperative and got detailed knowledge from Vaishali Mam regarding regulatory Affairs.

Vijaya Thorat

*****

Thank you Technobridge system for help me getting placed in Fortrea. whole team is very helpful and Vaishali mam gave the best guidance for improving skills and concepts. I highly recommend courses from Technobridge.

Website: https://www.technobridge.in/

Get Training & Placement Details Here- 9257035703

2. Global Pharma Academy

Offered by Global Pharma Academy in Pune, India, the Certificate Course in Drug Regulatory Affairs is a 3-month program designed to equip individuals with the knowledge and skills needed to navigate the complex world of pharmaceutical regulations. This course is suitable for graduates and working professionals in life sciences, pharmacy, medicine, and healthcare, aiming to bridge the gap between academic knowledge and the practical demands of the regulatory environment. Led by industry experts with over 10 years of experience, the curriculum covers various topics such as drug development regulations, marketing authorization procedures, and international regulatory requirements. By combining domain expertise with skill development, the program prepares students for a career in Drug Regulatory Affairs and offers placement assistance to help them secure relevant positions in the pharmaceutical sector.

Course: Diploma in Regulatory Affairs.

Duration: 3 Months.

Fees: 8999/-.

Training Mode: Online Live & Recorded.

Why Choose Global Pharma Academy for Drug Regulatory Affairs Course? Key features

o Learn from Industry Experts:

  • Best & Affordable Price
  • Job Assistance:
  • Experienced and qualified faculty.

Call Us for Free Career Counselling +91 9257035703

3. Mitcon Biopharma

Mitcon Biopharma offers an Online Regulatory Affairs course in Pune. This course is designed for professionals in the life sciences, pharmacy, and medical fields. Through the program, you’ll gain the knowledge and skills to navigate the complex world of regulatory requirements for developing, testing, manufacturing, marketing, and distributing pharmaceuticals and medical devices. You’ll delve into essential topics including Good Clinical Practices (GCP), key regulatory bodies (CDSCO, USFDA), drug and device applications, quality assurance in Regulatory Affairs, and post-market surveillance. By completing this course, you’ll develop the expertise to ensure compliance and facilitate a smooth approval process for new healthcare products.

Course: Diploma in Regulatory Affairs

Duration: 6 Months

Fees: 85,000/-.

Training Mode: Mitcon Biopharma offers classroom-based and online learning options (may vary).

Features: Mitcon Biopharma focuses on industry-aligned curriculum, practical skills development, and placement assistance (details to be confirmed).

  • Quality System Certification & Documentation
  • Validation & Qualification
  • Internal Audits & Customer Audits
  • Vendor audits & Vendor qualification
  • Laboratory set up, up-gradation to FDA, WHO- GMP, USFDA, MHRA, EDQM, GLP & GMP Standards.
  • Recruitment and training.
  • Raw material, Packing material, In Process materials & Finished products specification

Get Free Career Counselling Here +91 9257035703

4. Dysmech

Dysmech Consultancy Services (DCS) in Pune offers Advanced and Post Graduate Diploma programs in Clinical Research and Regulatory Affairs. Designed for aspiring professionals in clinical research and the pharmaceutical industry, these programs provide intensive, practical training (one-year or six-month options) on the duties of a Regulatory Affairs professional.

The curriculum equips you with a comprehensive understanding of the global regulatory framework for drugs and medical devices. You’ll develop the necessary skills for strategic planning in Regulatory Affairs throughout the product lifecycle, ensuring unwavering compliance with regulations at every stage — from research and development to marketing and distribution. DCS boasts a wide network and strong industry contacts, which can benefit graduates seeking job placement in the field.

Course: Certificate Course in Regulatory Affairs for Medical Devices

Duration: One Year / Six Months

Training Mode: Online

Why Choose Dysmech for Drug Regulatory Affairs Course? Key features

  • Better industrial training and skills,
  • Better knowledge of the industry,
  • In depth training of the industry regulations and work processes
  • Internationally certified with all market standards and integrity
  • Domain expertise and getting hands on practical exposure

5. Global Institute of Regulatory Affairs (GIRA)

The Global Institute of Regulatory Affairs (GIRA) in Pune offers a comprehensive Regulatory Affairs Online Course designed for life science graduates and final year students seeking careers in the pharmaceutical industry. This full-time program equips you with the in-depth knowledge and practical skills necessary to navigate the intricacies of drug regulations. The curriculum covers essential topics like Regulatory Affairs requirements for drug development, registration, and marketing across various regions.

GIRA’s program transcends theory, integrating real-world industry experiences directly into the coursework. This practical approach ensures you graduate with a strong understanding of how Regulatory Affairs are applied in everyday scenarios, giving you a competitive edge in the job market.

Course: Drug Regulatory Affairs Course

Duration: 6 Months

Fees: Full Time — 82,500/- (as per collegedunia.com)

Training Mode: Classroom cum Internship Program

To Get Training & Placement Details Call @+91 9257035703

6. Prorelix Education

Prorelix Education, a Pune-based institute recognized for excellence in Clinical Research training, offers a Post Graduate Diploma in Drug Regulatory Affairs. This course equips students with the knowledge and skills to navigate the complex world of drug regulatory affairs, ensuring they understand the processes involved in bringing drugs, devices, and other medical products to market.

The curriculum, designed with an international perspective, covers essential modules like clinical trials, pharmacovigilance, medical writing, and ICH-GCP guidelines. Prolix boasts industry-experienced faculty, practical training exercises focused on regulatory affairs, and placement assistance to prepare students for successful careers in this specific sector of the life sciences industry.

Course: Certificate Course in Regulatory Affairs.

Duration: 6 Months.

Training Mode: Online

7. Clini India

Clini India, a Pune-based institute, provides an online Regulatory Affairs Course designed for professionals in the pharmaceutical and life sciences sectors. The course caters to individuals with backgrounds in pharmacy (B.Pharm, M.Pharm, Pharm.D.), life sciences, physiotherapy (BPT, MPT), dentistry (BDS), Ayurveda (BAMS), homeopathy (BHMS), and medicine (MBBS). It equips participants with the knowledge and skills required to navigate the regulatory landscape of drug development in India.

Course: Certification Program in Regulatory Affairs.

Duration: 2 Months

Fees: 18000 + Registration Fee 2000/-.

Training Mode: Online

Why Choose Clini India for Drug Regulatory Affairs Course?

o Placement Support

Free Career Guidance After Life Science Degree @+91 9257035703

8. Elite Institute of Pharmacy Skills

The Elite Institute of Pharma Skills (EIPS) in Pune provides a Regulatory Affairs course designed to equip students with the knowledge and skills to navigate the complexities of the healthcare industry’s regulatory landscape. Their curriculum emphasizes the practical application of regulations, ensuring students gain a thorough understanding of how pharmaceutical companies, CROs, and other healthcare organizations navigate the process of bringing drugs, medical devices, and diagnostics to market. Led by experienced instructors, the program aims to prepare students for a successful and rewarding career in Regulatory Affairs. EIPS leverages its strong industry network and may even assist graduates with placement opportunities.

Course: Advanced Diploma In Drug Regulatory Affairs

Duration: 6 Months

Fees: 12000/-

Training Mode: Online

Why Choose Elite Institute of Pharmacy Skills for Drug Regulatory Affairs Course?

ELPS has taken the great responsibility to produce skilled professionals who would be trained essentially for this noble profession. Elite Institute of Pharma Skills offers a well thought out strategic course curriculum for students in Regulatory affairs. It is specifically designed to have a grip of how healthcare Industry of is run. They would also be provided with proper insight into the practical working. It wouldn’t be wrong to say that the students would find a competitive as well as friendly environment here to study and excel for the challenging world out there.

Get Regulatory Affairs Course Details @ +91 9257035703

9. Gratisol

Gratisol Life Sciences offers a Regulatory Affairs Course in Pune, equipping individuals to navigate the legal intricacies of the pharmaceutical industry. This program caters to both newcomers and experienced professionals seeking career advancement. The curriculum delves into national and international drug regulations, preparing participants for roles in pharma companies, regulatory bodies, and export-import agencies. Upon successful completion, participants receive a certificate and can leverage Gratisol’s career assistance program, including resume and interview coaching.

Course: Advanced Certified Program In Regulatory Affairs

Duration: 2 Months

Fees: 20000/-

Training Mode: Online

Why Choose Gratisol for Drug Regulatory Affairs Course? Key features

  • The course provides an interdisciplinary knowledge of pharmacy and law applicable in the field of pharmaceutical regulation at National and International levels.
  • The course prepares students to pursue careers in the pharmaceutical industry, drug licensing and control authorities, and export-import agencies dealing with pharmaceuticals.

To Get Training & Placement Details Call @+91 9257035703

10. Institute of Good Manufacturing Practices India (IGMPI)

The Institute of Good Manufacturing Practices India (IGMPI) provides a robust online Regulatory Affairs (RA) program designed to cater to diverse learning goals. This program is suitable for recent life sciences graduates or working professionals in the pharmaceutical, medical device, or food industries. IGMPI offers a range of options, from Post Graduate Diplomas to Industry Certificates, all receiving approval from the Quality Council of India (QCI).

The curriculum encompasses the entire Regulatory Affairs landscape, covering aspects like product development, manufacturing processes, documentation, and quality control. You’ll delve into the regulations governing research, testing, packaging, and everything in between. Through engaging online classes, case studies, and practical advice, IGMPI equips you with the knowledge and expertise to thrive in the field of Regulatory Affairs.

Course: Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA)

Duration: 1 Year

Fees: 90000/-

Training Mode: Online

Contact Us:

TechnoBridge Systems Pvt Ltd.

Contact No.: +91–9257035703

Email — info@technobridge.in

Facebook Page https://www.facebook.com/TechnoBridgeSystems/

Instagram Page https://www.instagram.com/technobridge_systems/

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Jaydeep Deva
Jaydeep Deva

Written by Jaydeep Deva

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I am Pharmacovigilance Associate at TechnoBridge Systems.