What is STEPUP?

Stepup Pharma Regulatory Consultant is an India based Pharmaceutical Regulatory Consultant, Located in Ahmedabad, Gujarat, India. Stepup is your single point as adjusting the regularly developing prerequisites of the Pharmaceutical Generic Industry in Ahmedabad. We associated with a wide assortment of regulatory consulting assignments.

Stepup Pharmatech always aspires to provide efficient and value-added support in obtaining faster Regulatory approvals for our clients.

Our administrative specialist helps customers by directing the product improvement in accordance with the county-specific prerequisites, data generation, report compilation for submission to different Regulatory Agencies everywhere throughout the world, reacting to the queries lastly getting the endorsement or enlistment of the product all under one rooftop.

We provide a creative, flexible, dedicated reliable regulatory and quality centric customer focused pharmaceutical services, which are second to none. Already entertaining inquiries into product development and sourcing, Stepup Pharmatech has already expanded its operations into the said areas.

Stepup Pharma Consultant provides Regulatory Affairs support to pharmaceutical companies across the globe on timely registration of their products globally.

“Intelligent strategies for global business”


In order to help you grow your business, our carefully selected experts can advise you in in the following areas:
Regulatory Services
Regulatory Affairs is a comparatively have been developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
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Business Development
The generic pharmaceutical industry with its ever-growing markets, provides tremendous business potential in terms of partnering, contract manufacturing, in-licensing and out-licensing and product development.
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An essential aspect of developing an efficient Regulatory team is to provide complete and updated knowledge on the current guidance and regulations. Also important is the skill in being able interpret and suffice the regulatory requirements for compilation of submissions and response to Deficiencies.
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GMP Audits
The requirement for GMP audits and a consistent global approach has never been greater. Global markets and international manufacture and supply of both raw materials and active pharmaceutical ingredients increase the complexity of supply chains. Addressing  GMP regulations effectively across international borders is easily facilitated by our network of local experts.
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Meet the people that are going to take your business to the next level.
Nirav Patel
Nirav Patel


Creative, detail-oriented, always focused.

Chintu Patel
Chintu Patel


Curious, tech-geeck and gets serious when it comes to work.

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