🌐 Global Regulatory Certifications

Advance Your Career with Global Regulatory Affairs & Pharma Industry Certifications

Industry-focused online certification programs designed for Pharma, Medical Device, Cosmetics, API, QA/RA, and Regulatory professionals worldwide.

✅Trusted by Pharma Students & Professionals

🏭Industry-Oriented Learning

🎓Career-Focused Certifications

5000+

Students Trained

Specialized Courses

20+

Global Markets

Rajshri Ojha

Founder — Raaj Pharma eLearning

Experienced pharma industry expert dedicated to empowering students & professionals through practical, industry-relevant regulatory affairs education across global markets.

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Our Programs

Specialized Certification Courses

Choose from our industry-designed programs covering every domain of pharmaceutical and medical device regulatory affairs.

Advanced Course in Global Regulatory Affairs

GRAAPIBiosimilarsOTC

Comprehensive global regulatory training covering API, formulations, biosimilars, OTC products, and medical devices for international pharma markets.

Master global regulatory frameworks & guidelines
Prepare dossiers for multiple market submissions
Career pathways in RA consulting & compliance

Regulatory Affairs [Formulation]

DossierMarket Auth

Learn end-to-end formulation regulatory processes, dossier preparation, submissions, compliance, and market authorization strategies.

Formulation dossier creation & review
Regulatory submission strategies
Roles in Regulatory Affairs departments

Regulatory Affairs [API]

APIDMFCompliance

Industry-oriented training focused on Active Pharmaceutical Ingredient regulations, DMF filings, compliance standards, and global submissions.

DMF preparation & filing expertise
Global API compliance standards
Opportunities in API manufacturing firms

$Regulatory Submissions: CTD-eCTD, ACTD, NeeS$

Regulatory Submissions: CTD-eCTD, ACTD, NeeS

CTDeCTDACTDNeeS

Master international submission formats and electronic regulatory documentation for global pharmaceutical approvals.

Electronic dossier publishing & validation
Multi-regional submission strategy
Roles as Regulatory Submission Specialists

GMP Auditor Course in Pharmaceutical

GMPAuditQA

Gain expertise in pharmaceutical quality systems, GMP compliance, audit procedures, documentation practices, and inspection readiness.

Conduct internal & vendor GMP audits
Inspection readiness & CAPA management
Roles as QA Auditors & Compliance Officers

Global Medical Device Regulation

EU MDRUS FDAIndiaASEAN

Understand medical device regulations across EU, USA, India, ASEAN, and Rest of World markets with practical compliance frameworks.

Multi-market regulatory pathway navigation
Technical documentation & CE marking
Careers in global MedTech RA

Medical Device QA/RA Course

ISO 13485Risk Mgmt

Specialized QA/RA training focused on medical device quality systems, ISO standards, regulatory pathways, and risk management.

ISO 13485 QMS implementation
Risk management per ISO 14971
Medical device RA & QA roles globally

QA/RA Course in Cosmetics

CosmeticsLabelingQA

Learn cosmetic product compliance, labeling, quality assurance, regulatory documentation, and international cosmetic standards.

Global cosmetics regulatory compliance
CPSR, labeling & claim substantiation
Roles in cosmetics QA/RA & compliance

Meet the Founder

Rajshri Ojha

Founder — Raaj Pharma eLearning

Experienced pharma industry expert dedicated to empowering students and professionals through practical, industry-relevant regulatory affairs education across global markets. With deep expertise spanning formulations, API, medical devices, and cosmetics regulation, Rajshri Ojha has built a platform that bridges the gap between academic knowledge and industry demands.

🌍

Extensive experience in global regulatory affairs across US, EU, India, ASEAN & RoW markets

🎓

Trained 5000+ pharma students & working professionals for global career opportunities

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Practical, case-study driven curriculum reflecting real pharmaceutical industry practices

Student Success

What Our Students Say

Join thousands of pharma professionals who have transformed their careers with Raaj Pharma eLearning.

★★★★★

"The Global Regulatory Affairs course gave me the practical knowledge I needed to crack a regulatory role at an MNC. The content is genuinely industry-relevant."

Priya Sharma

Regulatory Affairs Executive, Mumbai

★★★★★

"I transitioned from QA to RA after completing the CTD-eCTD course. Rajshri Ma'am's teaching style makes complex topics easy to understand."

Arjun Mehta

Regulatory Submissions Specialist, Hyderabad

★★★★★

"The Medical Device Regulation course is the most comprehensive program I've found. Perfect for anyone looking to break into the MedTech industry."

Sneha Patil

Medical Device RA Professional, Pune