About Nishi chawla
Nishi is an expert content writer having an expertise in writing Business Legal Compliances, Certifications, and Registrations. She is an expert in BIS, EPR, Medical Devices, Cosmetics, Drugs, and Import Export having completed her bachelor’s of commerce from one of the most prestigious universities in India, University of Delhi. She has been writing content since 2019 for multiple firms including Agile Regulatory, Creation Infoways, and Devlofox Technologies.
Drug License for Medical Equipment in India
- 03 Feb 2026 |
- Reading Time: 5 Minutes
A Drug License for medical equipment in India is mandatory for manufacturing, importing, selling, or distributing notified medical devices. Issued by the Central Drugs Standard Control Organization (CDSCO) or State Drug Authority, this license ensures tha
Read moreMedical Device Distributor License in India Registration Process
- 03 Feb 2026 |
- Reading Time: 6 Minutes
The Medical Device Distributor License in India registration process involves obtaining approval from the Central Drugs Standard Control Organization (CDSCO) to legally distribute medical devices. The process includes documentation, compliance with Medica
Read moreMedical Device Manufacturing License Registration in India (2026 Update)
- 03 Feb 2026 |
- Reading Time: 7 Minutes
Medical device manufacturing in India now requires mandatory licensing, compliance with MDR 2017, quality systems, registration, and regulatory approval from CDSCO by 2026.
Read moreBest EPR Consultant in Gurugram and Haryana in 2026
- 02 Feb 2026 |
- Reading Time: 6 Minutes
Find the best EPR consultant in Gurugram and Haryana in 2026 to help your business comply with Extended Producer Responsibility regulations efficiently and effectively.
Read moreLMPC Registration Procedure in India (2026 Update)
- 02 Feb 2026 |
- Reading Time: 7 Minutes
LMPC (Limited Manufacturing & Production Certificate) registration in India allows businesses to legally manufacture and sell specific products. The process involves submitting an application, providing business and compliance documents, and obtaining ap
Read moreBest EPR Consultant in Noida and UP in 2026
- 02 Feb 2026 |
- Reading Time: 6 Minutes
Looking for the best EPR consultant in Noida and UP in 2026? Agile Regulatory offers expert guidance, compliance support, and hassle-free Extended Producer Responsibility solutions for businesses across the region.
Read moreBest CDSCO License Registration Consultant in Delhi (2026)
- 29 Jan 2026 |
- Reading Time: 7 Minutes
We are the leading CDSCO license registration consultants in Delhi, providing end-to-end support for pharmaceutical, medical device, and cosmetic businesses. Our experts ensure timely approvals, proper documentation, and full compliance with CDSCO regulat
Read moreWhat is the Bureau of Indian Standards: Objective, Purpose, Services, and Registration
- 29 Jan 2026 |
- Reading Time: 5 Minutes
The Bureau of Indian Standards (BIS) is India’s national standards body responsible for developing quality standards, ensuring product safety, and promoting consumer trust through certification and registration services.
Read moreBest BIS Consultant in Delhi and Haryana in 2025
- 29 Jan 2026 |
- Reading Time: 5 Minutes
We provide expert BIS consultancy in Delhi and Haryana, helping businesses obtain Bureau of Indian Standards certification quickly and efficiently. Our experienced consultants guide you through compliance, documentation, and registration, ensuring a smoot
Read moreCDSCO Registration Fees in India in 2026
- 29 Jan 2026 |
- Reading Time: 5 Minutes
In 2026, CDSCO registration fees in India vary by category, including ₹5 lakh for CRO registration, clinical trial fees per phase, and device/drug import or cosmetic registration charges as mandated by CDSCO.
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