You know the frustration.
You want to grow in your RA/QA career, but the options are discouraging. Onsite training programs cost a fortune and require time off work. Online courses dump information without context—leaving you with certificates but no real confidence. And when you’re stuck on a real-world problem, there’s no one to ask.
You’re expected to navigate complex regulations, implement quality systems, and make decisions that affect patient safety—often with minimal structured guidance. The learning curve is steep, and the stakes are high.
We built NeuLearn because this gap shouldn’t exist.
NeuLearn is a dedicated learning platform for Regulatory Affairs and Quality Assurance professionals working in the medical device industry.
We don’t just offer courses. We offer a complete learning experience—combining expert instruction, hands-on practice, and ongoing mentorship. Every course is designed to build practical skills you can apply immediately, not just theoretical knowledge that looks good on paper.
All courses scripted and validated by subject matter experts from the industry.
Every course includes weekly live classes where you can ask questions, discuss scenarios, and learn alongside peers facing similar challenges. No more pausing videos and hoping you understood correctly.
Your assignments and quizzes aren't just auto-graded and forgotten. Our mentors review your work, provide feedback, and help you understand where you went wrong—and why it matters.
Each course comes with downloadable templates, handbooks, and reference materials designed for real-world application. These aren't generic documents—they're tools you can adapt for your own projects.
Learning doesn't stop when the module ends. Our learning community gives you a space to discuss challenges, share experiences, and connect with fellow RA/QA professionals who understand what you're dealing with.
I’ve spent years working in Regulatory Affairs and Quality Assurance—preparing technical documentation, navigating regulatory submissions across multiple markets, and helping medical device companies bring safe products to patients.
Along the way, I watched talented professionals struggle to find quality training. I saw people pay for expensive programs that didn’t deliver, or piece together knowledge from scattered online resources without any guidance. The industry demands expertise, but the path to gaining that expertise was broken.
NeuLearn exists to fix that. I wanted to create the learning platform I wish I’d had—one that combines deep regulatory knowledge with practical application and real human support.
This isn’t about building a course library. It’s about building careers.
FOUNDER & CEO
Dr. Samundeeswari is a Regulatory Affairs and Quality Systems professional with a strong academic and research background and extensive experience in scientific documentation and training. She holds a PhD in Inorganic Chemistry from Freie Universität Berlin, Germany (Magna Cum Laude).
Following her doctorate, she completed an Honors Postdoctoral Research Fellowship at the Dahlem Research School, Freie Universität Berlin, conducting research in diagnostic medicine using ⁹⁹ᵐTc radiopharmaceuticals. She later completed a postdoctoral research fellowship at the University of Nevada, Las Vegas (USA), where she led independent research on radioactive and non-radioactive metal fluoride complexes and radioactive waste treatment, and mentored graduate and undergraduate students, with mentees successfully awarded competitive summer research scholarships.
She has authored 28 peer-reviewed publications and delivered international conference presentations, reflecting strong expertise in scientific writing, literature evaluation, and evidence-based analysis.
Dr. Samundeeswari applies this foundation to medical device regulatory practice, specializing in EU MDR clinical evaluation and technical documentation, including CEPs, CERs, literature search and appraisal, and alignment with MDCG guidance and ISO standards. She develops structured, compliance-focused training programs with a strong emphasis on practical, audit-ready documentation.
Atonu Dutta is the founder of Neujin Solutions. He is a Graduate in Electrical and Electronics Engineering and a Masters in Mathematics from BITS Pilani and also holds a post-graduation in Management from the Indian Institute of Management, Indore. He has worked in the areas of RA and QA pertaining to medical devices for over 18 years, out of which he spent more than a decade in a major European Notified Body.
He has been a Lead Assessor, Auditor and Trainer during his stint with the Notified Body, where he assessed an enormous variety of medical devices and conducted over a 1000 mandays of audit, globally.
Aakash Jindal is the Founder of iMDR MedTech Consultancy, a global consulting firm. In his role, he is supporting medical device manufacturers with market access strategies and Quality Management System (QMS) implementation across major regulatory jurisdictions. He brings hands-on expertise across the end-to-end medical device lifecycle, including design and development, regulatory submissions, post-market compliance, and lifecycle change management.
Aakash has worked extensively on global regulatory pathways, technical documentation, cross-functional coordination, and regulatory impact assessments, enabling efficient and compliant market entry for medical technologies. He holds a Master’s degree in Medical Devices and combines strong regulatory, quality, and systems-thinking perspectives, making his instruction both practical and strategically aligned with real-world regulatory expectations.
NeuLearn is a brand of Neujin Solutions, a consultancy dedicated to helping medical device companies navigate regulatory and quality challenges. Our training content draws on real consulting experience—the same expertise we bring to our clients, now accessible to individual professionals looking to grow.
Whether you’re new to RA/QA and building your foundation, or an experienced professional looking to deepen your expertise, NeuLearn has a path for you.
