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Healthcare & Pharma Industry

Industry Services

Hospital & Diagnostic Center Licensing

Home /Healthcare & Pharma Industry / Hospital & Diagnostic Center Licensing

At Startup Solicitors LLP, one of the best law firms in Jaipur, we provide specialized legal and CA services for India's booming healthcare and pharma industry. From pharmaceutical companies and hospitals to telemedicine platforms and medical device distributors, our top advocates in Jaipur deliver end-to-end support for licenses, regulatory compliance, clinical approvals, and digital-health legal frameworks. Our deep expertise in healthcare law in India ensures your business operates legally, efficiently, and with full compliance confidence.

Navigating India’s complex healthcare regulations, drug and cosmetic laws, and medical council guidelines can be overwhelming for new and established businesses. Our expert team simplifies the entire process—guiding you through drug manufacturing license applications, clinical trial registrations, telemedicine practice compliance, and navigating the legalities of medical device import and distribution. Whether you're launching a pharmaceutical company, a hospital, or a diagnostic center, Startup Solicitors LLP is your trusted legal partner for all healthcare and pharma compliance and licensing needs in India.

Why the Healthcare & Pharma Industry Trusts Us

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Regulatory expertise

Our team has over a decade of experience in the healthcare and pharma sector.

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PAN-India licensing support

We have a proven track record of successfully guiding healthcare and pharma businesses.

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Experience with CDSCO, NPPA, FSSAI & Health Ministry bodies

We provide integrated support, from company formation to ongoing compliance.

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Compliance documentation & audit support

We ensure your legal and compliance processes are completed efficiently.

Frequently Asked Questions (FAQs)

Healthcare & Pharma Industry
1. How to apply for Drug Manufacturing License in India?
To apply for a drug manufacturing license in India, you need to apply to the State Drug Control Authority. The application must be accompanied by a host of documents, including the layout of the premises, details of the manufacturing equipment, and the qualifications of the technical staff. Our Healthcare legal services cover all these requirements.
2. Is CDSCO approval required for medical devices?
Yes, CDSCO approval is required for medical devices in India. The Central Drugs Standard Control Organization (CDSCO) is the national regulatory body for Indian pharmaceuticals and medical devices. Our Healthcare legal services cover all these requirements.
3. Legal rules for telemedicine practice in India
The legal rules for telemedicine practice in India are governed by the Telemedicine Practice Guidelines, which were issued by the Board of Governors in supersession of the Medical Council of India. Our Healthcare legal services cover all these requirements.

Propel Your Healthcare & Pharma Business with Expert Legal & CA Services

Partnering with us means more than just compliance – it’s about gaining a strategic partner for your healthcare and pharma business. Our services help you:

Contact us today to learn more about how our specialized services for the healthcare and pharma industry in India can add value to your business.

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