- info@syntiqglobal.com
- Block no.15/61G , Ist Floor, Sri Andal Avenue. Coimbatore 641016
Strong product development must be supported by accurate regulatory, technical, and scientific documentation.
At Syntiq Global, we bridge science and compliance — ensuring your innovation is market-ready.
Develop smart. Document precisely. Approve faster.
We assist with:
• Regulatory pathway planning during product development
• Formulation and product development regulatory alignment
• Device development documentation support
• Classification and regulatory feasibility assessment
• Product lifecycle development strategy
We integrate regulatory intelligence early in your R&D process to prevent costly delays.
We prepare structured and submission-ready documentation including:
• CTD / eCTD dossiers
• Clinical evaluation reports
• Technical files and design dossiers
• Risk management documentation
• SOP development and QMS documentation
• Regulatory response letters
Clear. Compliant. Scientifically accurate.
Our writing and documentation support aligns with:
• CDSCO requirements
• US FDA submission formats
• EU MDR documentation structure
• ISO 13485 documentation standards
• GMP documentation practices
We ensure documentation withstands regulatory review and audit scrutiny.
Let Syntiq Global transform complex data into regulatory-ready submissions.
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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