Seedling RA Solutions

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Welcome to Seedling ra Solutions

Seedling RA Solutions is one of the well-respected and prominent Regulatory Consulting organizations for the life sciences industry.

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About us

CTD

Common Technical Document (Product Dossier) is an Integral Part of any registration application for Marketing Authorization.

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About us

Drug Master File – DMFs

Drug Master File is a technical document containing CMC part – chemistry, Manufacturing & control of an Active pharmaceutical ingredient.

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About us

Food Supplements Dossiers

Classification of Food Supplements Dossiers is a challenging task, since it is dependent on several factors

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About us

Dossier - CTD, ACTD & ROW

Seedling RA solutions is a global leader in regulatory consulting and dossier solutions for export registration

bn1

Welcome to Seedling Ra Solutions

Seedling RA Solutions is one of the well-respected and prominent Regulatory Consulting organizations

About us

bn1

CTD

Common Technical Document (Product Dossier) is an Integral Part of any registration application for Marketing Authorization.

bn1

Drug Master File – DMFs

Drug Master File is a technical document containing CMC part – chemistry, Manufacturing

bn1

Food Supplements Dossiers

Classification of Food Supplements Dossiers is a challenging task, since it is dependent on several factors

bn1

Dossier - CTD, ACTD & ROW

Seedling RA solutions is a global leader in regulatory consulting and dossier solutions for export registration

Welcome to the Seedling RA Solutions

Seedling RA Solutions is a comprehensive regulatory consultancy company based in Delhi, India.

Overview
Indian Pharmaceutical Industry has made great strides as one of the largest exporters of generics in the world. The Indian Pharmaceutical industry now faces the challenges of unpredictable product pipelines, increasingly competitive markets, and uncertain policy and regulatory environments.

OUR FOCUS
We work in close collaboration with our clients to provide innovative and cost effective solutions to help maintain their competitive advantage from early stage of product development right through to licensing, manufacture in short through out the life cycle of the product.

Our Services

Seedling RA Solutions is one of the well-respected and prominent Regulatory Consulting organizations for the life sciences industry.

All services are customized and available on a modular basis meeting the specific requirements of our clients.
We work closely with your team and help develop solutions tailored to meet your requirements.

CTD

Common Technical Document is an Integral Part of any registration application for Marketing Authorization.

Drug Master File – DMFs

Drug Master File is a technical document containing CMC part – chemistry, Manufacturing & control of an Active pharmaceutical

NUTRACEUTICALS / FOOD SUPPLEMENTS

Classification of Food Supplements Dossiers is a challenging task, since it is dependent on several factors like intended use.

ACTD

Seedling RA solutions is a global leader in regulatory consulting and dossier solutions for export registration

ROW

Seedling RA Solutions is provide you quality support for registration dossiers in ROW countries.

WRITING / REVIEW

Seedling RA solutions is making your documentation more effective and quality driven.

SUPPORTIVE SERVICES

CORE SERVICES

“We are driven by a desire to excel and exceed customer expectations, provide a joyous working environment for our people and empower them to think big and set ambitious goals. We want to achieve all this in an environment that promotes integrity”