Syntiq Global – Regulatory Excellence

Accelerating Regulatory Approvals. Securing Compliance. Enabling Growth.

End-to-end regulatory, clinical, and research consulting for highly regulated healthcare industries across India and global markets.
Years Experience
0 +
Professional Doctor
0 +
Happy Patients
0 M+
15+
Years of Experience
POSITIONING STATEMENT

Regulatory Complexity Should Never Delay Innovation.

At Syntiq Global, we transform regulatory challenges into structured, approval-ready strategies. Our approach ensures clarity, compliance, and confidence — enabling seamless market entry and sustainable growth.

COMPREHENSIVE REGULATORY & SCIENTIFIC SOLUTIONS

From licensing to lifecycle management, we support every stage of your product journey with precision and strategic insight.
Regulatory Licensing

Structured licensing and approval pathways for importers and manufacturers under CDSCO, MDR 2017, FSSAI, and global regulatory frameworks.

Authorized Agent Services

Your official regulatory presence in India — managing submissions, authority communication, renewals, and post-approval compliance.

Compliance & Quality Support

Inspection-ready systems aligned with Indian regulations and international standards including ISO 13485 and GMP.

Clinical & Regulatory Support

Strategic guidance from clinical trial applications to marketing authorization and post-market compliance.

Research & Development Services

Science-driven product development supported by regulatory intelligence and documentation excellence.

Medical Writing

Precise, structured, and submission-ready documentation for clinical, regulatory, and scientific communication.

GLOBAL REGULATORY EXPERTISE

Aligned with Global Regulatory Standards
CDSCO | US FDA | EU MDR | MHRA | ISO 13485 | FSSAI
Built for India. Ready for the World.

Why Industry Leaders Choose Syntiq Global

Strategic Regulatory Planning
Precision Documentation & Dossier Excellence
Reduced Approval Delays
Lifecycle Compliance Management
Global Regulatory Intelligence
We don’t just file applications — we build regulatory strategy.
15+
Years of Experience
DIFFERENTIATOR STATEMENT

Science-Driven. Compliance-Focused. Market-Ready.

Our multidisciplinary expertise integrates regulatory intelligence, clinical insight, research excellence, and structured documentation to accelerate approvals while minimizing risk.

Regulatory excellence is not optional — it is strategic.

OUR STRUCTURED APPROACH

A Clear Pathway to Regulatory Success

Regulatory Assessment
Strategy Development
Documentation & Technical Review
Submission & Authority Liaison
Approval & Lifecycle Support
Clear process. Controlled timelines. Confident outcomes.
Happy Patients
0 M+
Member Active
0 K+
Professional
0 +
Years Experience
0 +
Testimonial

Client Feedback & Reviews

Ready to Enter or Expand in Regulated Markets?

Let’s build your regulatory roadmap with clarity, compliance, and confidence.

Get in Touch

Consultation Request

Have a regulatory challenge or project in mind?
Share your requirements and our team will respond promptly.

Let's Talk

Phone : +919629542753
Phone : +918903282797

Mail Us

info@syntiqglobal.com