- info@syntiqglobal.com
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Structured licensing and approval pathways for importers and manufacturers under CDSCO, MDR 2017, FSSAI, and global regulatory frameworks.
Your official regulatory presence in India — managing submissions, authority communication, renewals, and post-approval compliance.
Inspection-ready systems aligned with Indian regulations and international standards including ISO 13485 and GMP.
Strategic guidance from clinical trial applications to marketing authorization and post-market compliance.
Science-driven product development supported by regulatory intelligence and documentation excellence.
Precise, structured, and submission-ready documentation for clinical, regulatory, and scientific communication.
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.
We provide tailored regulatory solutions for:
Let’s build your regulatory roadmap with clarity, compliance, and confidence.
Have a regulatory challenge or project in mind?
Share your requirements and our team will respond promptly.
Phone : +919629542753 Phone : +918903282797
info@syntiqglobal.com
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