Global Pharmaceutical Regulatory Services

Accurate, Compliant & Fast Regulatory Approvals Worldwide

RAGS Global Solutions provides high-quality, premium regulatory support to pharmaceutical and nutraceutical companies ensuring seamless approvals across 40+ countries.

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100+

Successful Submissions

40+

Countries Covered

98%

Approval Success Rate

3+

Years of Experience

Our Core Expertise

Global Regulatory Compliance

Expertise in FDA, EMA, ICH, WHO, ASEAN, GCC and other international regulatory standards across multiple jurisdictions.

Comprehensive Dossier Preparation

CTD, ACTD, eCTD and country-specific dossier formats prepared with precision and regulatory accuracy.

Expedited Approval Process

Streamlined processes ensuring 75% faster turnaround without compromising quality or compliance requirements.

Our Key Services

Dossier Preparation

Complete regulatory dossier preparation for global submissions including CTD, eCTD, ACTD, and country-specific formats.

Common Technical Document (CTD)
ASEAN Common Technical Document (ACTD)
Electronic CTD (eCTD)
Country-specific formats

Variation Filing

Comprehensive variation filing services for post-approval changes and regulatory updates.

Type IA & IB Variations
Type II Major Variations
Post-approval changes
Regulatory compliance checks

Regulatory Consulting

Strategic regulatory consulting and compliance advisory for pharmaceutical and nutraceutical products.

Regulatory strategy development
Compliance gap analysis
Market entry planning

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Ready to Accelerate Your Regulatory Approvals?

Partner with RAGS Global Solutions for expert regulatory support and seamless product approvals worldwide. Our team of regulatory experts is ready to guide you through complex regulatory landscapes.

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