Syntiq Global – Regulatory Excellence

Integrated Regulatory, Scientific, and Drug Discovery Solutions

Supporting pharmaceutical, medical device, cosmetic, and nutraceutical industries through regulatory expertise, research innovation, and AI-driven drug discovery.

About SYNTIQ Global

SYNTIQ Global is a multidisciplinary scientific and regulatory solutions provider supporting the pharmaceutical, medical device, cosmetic, and nutraceutical industries. We combine regulatory expertise, scientific research, and AI-driven drug discovery technologies to accelerate product development and global market access.

Our services span regulatory submissions, product development, scientific consulting, and computational drug discovery, enabling organizations to transform innovative concepts into globally compliant products.

COMPREHENSIVE REGULATORY & SCIENTIFIC SOLUTIONS

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

Regulatory Affairs & Global Filings

Strategic regulatory guidance and documentation support for pharmaceuticals, medical devices, cosmetics, cosmeceuticals, and nutraceutical products to facilitate approvals in India and international markets.

Medical Device Regulatory & Authorized Agent

Regulatory assistance for medical device registration, technical documentation, and authorized agent representation for manufacturers seeking regulatory approval and compliant market entry.

Laboratory Licensing & Approvals

Support for obtaining regulatory licenses and approvals for analytical laboratories, testing laboratories, and drug testing facilities, including guidance on regulatory documentation and compliance requirements.

Analytical Testing Support

Scientific and regulatory support for analytical testing of pharmaceuticals, medical devices, cosmetics, cosmeceuticals, and nutraceutical products to ensure product quality, safety, and regulatory compliance.

Clinical & Regulatory Support

Assistance with regulatory documentation, technical submissions, and regulatory strategy to support product development and regulatory review processes.

Compliance & Quality Systems

Guidance on regulatory compliance, quality management systems, and documentation practices aligned with applicable regulatory frameworks and standards.

Medical & Scientific Writing

Professional preparation of scientific manuscripts, regulatory dossiers, technical reports, and clinical documentation to support research activities and regulatory submissions.

Nutraceutical & Cosmeceutical R&D

Scientific support for product innovation including research evaluation, formulation concepts, and regulatory documentation for nutraceutical and cosmeceutical products.

AI-Driven Drug Discovery

Application of computational tools and data-driven approaches to support early-stage drug discovery, molecular analysis, and translational research initiatives.

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.

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.

INDUSTRIES WE SERVE

Specialized Expertise Across Regulated Healthcare Sectors

We provide tailored regulatory solutions for:

Medical Devices

Nutraceuticals & Health Supplements

Cosmetics

In Vitro Diagnostics (IVD)

Drugs

Biologicals & Vaccines

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.

Testimonial

Client Feedback & Reviews

Syntiq made the entire regulatory process simple and stress-free for us. Their team was quick to respond, and we had all the guidance we needed for our product registration. Highly recommended for anyone looking to navigate the complexities of compliance.

Sarah M.Business Owner

Working with Syntiq was an excellent experience. They helped us with all the legal requirements for importing medical devices, and their expert advice ensured smooth and efficient approval. I will definitely use their services again.

John DMedical Equipment Supplier

As a food importer, it was crucial to meet FSSAI standards. Syntiq made the process clear and easy. Their expertise ensured we were fully compliant, and their support helped us avoid potential delays.

Maria L.Importer

The team at Syntiq was invaluable during the importation of our cosmetics line. They guided us through every step, ensuring that we met all regulatory requirements. Their professionalism is unmatched, and they are always ready to help.

Emma T.Cosmetics Brand Owner

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

8903282797

Mail Us

info@syntiqglobal.com