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📝 Nishi chawla

About Nishi chawla


Nishi ChawlaNishi 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.

ISI Mark Certificate for Food Products Registration Process
  • 07 Aug 2025
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  • Reading Time: 5 Minutes

The ISI mark certificate for food products ensures that they meet BIS quality and safety standards. The registration process involves identifying the relevant Indian standard, submission of documents, products testing and submission of application with BI

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BIS certification for chemicals in India New Standard Updates 2024-2025
  • 07 Aug 2025
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  • Reading Time: 6 Minutes

The BIS Certification for chemicals in India has undergone significant updates during 2024–2025, introducing revised standards for various chemical substances to enhance product quality and safety. These changes aim to strengthen regulatory compliance for

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Cosmetics Export from India in 2025: Documents, Process, and Fees
  • 06 Aug 2025
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  • Reading Time: 5 Minutes

The export of cosmetics from India in 2025 includes a structured process that includes the preparation of necessary documents such as IEC (Import Export Code), Product Registration Certificate and Challan. Exporters should follow labeling norms, quality s

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BIS Certification for Stainless Steel Seamless pipes and tubes for general service IS 17875: 2022
  • 06 Aug 2025
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  • Reading Time: 6 Minutes

BIS Certification under IS 17875:2022 is mandatory for stainless steel seamless pipes and tubes used for general services. It ensures product quality, compliance, and trust in both domestic and international markets.

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PSARA License West Bengal: Requirements, Fees, and Application Timeline
  • 05 Aug 2025
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  • Reading Time: 5 Minutes

Looking to start a private security agency in West Bengal? The PSARA License is a mandatory legal requirement. This guide covers eligibility, documents, application steps, and how Agile Regulatory can assist with smooth PSARA registration in West Bengal.

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PSARA License in Karnataka: Eligibility, Process, and Timeline
  • 05 Aug 2025
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  • Reading Time: 7 Minutes

Getting PSARA license in Karnataka is an essential legal requirement for anyone planning to start a private security agency in the state. This article explains the eligibility criteria, step-by-step application process and the required timeline for approv

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Legal Metrology Registration in Jharkhand – Compliance, Process & Consultant Support
  • 04 Aug 2025
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  • Reading Time: 7 Minutes

Get your Legal Metrology Registration in Jharkhand to ensure compliance with packaging and weight & measurement laws. Agile Regulatory offers expert support for smooth and timely registration for manufacturers, importers, and packers.

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Legal Metrology Certification in Kerala
  • 04 Aug 2025
  • |
  • Reading Time: 6 Minutes

The Legal Metrology Department Kerala ensures accuracy in weights and measures used in trade. It regulates packaging, labeling, and measurement standards across the state to protect consumer rights and promote fair business practices.

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IS 17876:2022 – BIS Certification for Stainless Steel Welded Pipes and Tubes for General Service
  • 31 Jul 2025
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  • Reading Time: 5 Minutes

IS 17876: 2022 is an Indian standard that specifies the requirements for stainless steel welded pipes and tubes for general service applications. To ensure compliance with quality and safety standards, manufacturers must obtain BIS ISI certification under

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Revised Schedule M in Pharmacy Guidelines 2023
  • 31 Jul 2025
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  • Reading Time: 7 Minutes

The Revised Schedule M under Pharmacy Guidelines 2023 introduces stricter norms for Good Manufacturing Practices (GMP) in India. It focuses on improved infrastructure, quality control, documentation, and staff training for pharmaceutical manufacturers. Th

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