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RNI Certificate in India – A Complete Guide by Agile Regulatory

What Is the RNI Certificate?

The RNI Certificate is an official document issued by the Registrar of Newspapers for India under the Press and Registration of Books Act, 1867. It acts as legal proof that your publication title is registered and permitted to be published and circulated.

Without this certificate, any printed newspaper or magazine is considered unauthorized in India. So, whether you’re a passionate…

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Added by Agile Regulatory on April 7, 2025 at 6:35am — No Comments

Step-by-Step Guide to One Person Company Registration

Starting a business can be an exciting journey, and for solo entrepreneurs in India, the One Person Company (OPC) model offers a perfect combination of control and compliance. Introduced under the Companies Act, 2013, OPC enables a single individual to operate a corporate entity with limited liability and distinct legal status. This guide walks you through each step of registering an OPC in India, ensuring you meet all the legal requirements smoothly and…

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Added by Agile Regulatory on April 7, 2025 at 3:16am — No Comments

Model Approval Certificate: Everything You Need to Know

What is a Model Approval Certificate ?

The Model Approval Certificate is an official approval granted by the Directorate of Legal…

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Added by Agile Regulatory on April 4, 2025 at 6:21am — No Comments

Why APEDA Registration is Essential for Food Exporters

India has long been recognized as a global agricultural powerhouse, contributing significantly to the international trade of fruits, vegetables, processed foods, cereals, and other agri-products. As the demand for Indian food products continues to grow across global markets, food exporters need to align themselves with the regulatory and promotional frameworks established by the Government of India. One such important body is APEDA – the Agricultural…

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Added by Agile Regulatory on April 4, 2025 at 5:08am — No Comments

UP Drug License: A Comprehensive Guide

Introduction

A UP Drug License is a legal requirement for businesses involved in the sale, distribution, and manufacturing of pharmaceutical products in Uttar Pradesh. The license is issued by the Food Safety and Drug Administration (FSDA), Uttar Pradesh, under the Drugs and Cosmetics Act, 1940. This guide provides a detailed overview of the types of drug licenses, eligibility criteria, application process, required documents, and how Agile Regulatory can assist…

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Added by Agile Regulatory on April 3, 2025 at 7:27am — No Comments

Company Registration in India: Types, Benefits, and Legal Requirements

Why Register a Company in India?

Company registration offers several advantages, including:

  • Legal Recognition: A registered company is recognized by law and has a separate legal identity.

  • Limited Liability Protection: The liability of shareholders is limited to their shareholding.

  • Tax…

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Added by Agile Regulatory on April 3, 2025 at 4:53am — No Comments

RNI Registration: Why It's Essential for Print and Online Publications.

If you are planning to start a newspaper, magazine, or any periodical publication in India, obtaining (Registrar of Newspapers for India) RNI registration is a crucial step. This registration is mandatory under the Press and Registration of Books Act, 1867 and is…

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Added by Agile Regulatory on April 2, 2025 at 5:33am — No Comments

Cosmetics Import License in India: A Complete Guide by Agile Regulatory

Introduction

The demand for international cosmetics brands in India has grown significantly over the past decade. However, to legally import and sell cosmetic products in India, businesses must obtain a Cosmetics Import License from the Central Drugs Standard Control Organization (CDSCO). This license ensures compliance with safety and quality standards set under the…

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Added by Agile Regulatory on April 1, 2025 at 6:00am — No Comments

EPR Certification for the Toy Industry: A Comprehensive Guide

Introduction

Extended Producer Responsibility (EPR) is a regulatory framework designed to ensure that manufacturers, importers, and brand owners take responsibility for the end-of-life management of their products. In the toy sector, where plastic and electronic components are prevalent, EPR certification is essential to promote sustainable waste disposal and meet regulatory compliance. Agile Regulatory simplifies the EPR certification process, helping businesses…

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Added by Agile Regulatory on March 31, 2025 at 7:57am — No Comments

Beyond the Bureaucracy: Unlocking Market Access with Expert BIS Certification Guidance.

Introduction

In an evolving regulatory landscape, businesses must navigate an intricate web of compliance requirements to ensure seamless market operations. The Bureau of Indian Standards (BIS) plays a crucial role in maintaining quality, safety, and reliability for products in India. As regulatory norms become more stringent, businesses face increasing challenges in obtaining and maintaining BIS certification. Agile Regulatory, a trusted…

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Added by Agile Regulatory on March 27, 2025 at 12:48am — No Comments

Beyond Recognition: How MSME Registration Empowers Small Enterprises

Introduction :

Micro, Small, and Medium Enterprises (MSMEs) play a crucial role in the global economy, contributing significantly to employment generation, GDP growth, and innovation. In India, MSME registration provides businesses with numerous benefits, including financial support, subsidies, and easier access to credit. As we move forward, evolving policies, technological advancements, and economic trends are set to reshape the future of…

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Added by Agile Regulatory on March 26, 2025 at 3:09am — No Comments

Factory Act Registration: Online application help

Introduction

The Factories Act, 1948, is a comprehensive legislation enacted to regulate labor welfare, safety, and working conditions in manufacturing establishments. It mandates Factory Act Registration for units meeting specific criteria, ensuring legal compliance and protection of workers. However, the implementation of the Act varies across states in India due to different industrial landscapes, state-specific rules, and administrative…

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Added by Agile Regulatory on March 25, 2025 at 12:32am — No Comments

RNI Registration: Key Documents and Requirements

Introduction

The print media industry in India is regulated by the Registrar of Newspapers for India (RNI), which ensures that newspapers and periodicals comply with the Press and Registration of Books Act, 1867. If you are planning to start a newspaper, magazine, or journal, obtaining RNI registration is a mandatory step. This article provides a comprehensive guide to RNI registration, covering its importance, eligibility, application process,…

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Added by Agile Regulatory on March 24, 2025 at 12:25am — No Comments

APEDA Registration Renewal: Ensuring Continuous Export Operations

For businesses engaged in agricultural exports, maintaining a valid APEDA registration is essential for uninterrupted operations. The Agricultural and Processed Food Products Export Development Authority (APEDA) provides exporters with a Registration-cum-Membership Certificate (RCMC), which facilitates global market access. While APEDA registration is…

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Added by Agile Regulatory on March 20, 2025 at 5:28am — No Comments

Choosing the Right Certification Body for Your RoHS Needs

The Restriction of Hazardous Substances (RoHS) directive plays a crucial role in ensuring that electrical and electronic products meet environmental safety standards. Compliance with RoHS regulations is not just a legal necessity but also an essential step in gaining market access in regions like the European Union, India, and other countries that have adopted similar regulations.

One of the most critical decisions in the compliance journey is selecting the right…

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Added by Agile Regulatory on March 19, 2025 at 3:00am — No Comments

UP Pollution Control Board Consent: CTE & CTO Explained

The Uttar Pradesh Pollution Control Board (UPPCB) plays a crucial role in regulating industries and ensuring environmental compliance in the state. Businesses that deal with manufacturing, processing, or any activity that may impact the environment must obtain Consent to Establish (CTE) and Consent to Operate (CTO) under the Air and Water (Prevention and Control of…

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Added by Agile Regulatory on March 18, 2025 at 5:14am — No Comments

Lifestyle Changes to Reduce Breast Cancer Risk

Breast cancer is influenced by a combination of genetic, environmental, and lifestyle factors. While you can't change your genetic makeup, making certain lifestyle changes can significantly reduce your risk of developing breast cancer. Here are some detailed tips on diet, exercise, and other lifestyle choices that can help lower the risk.

Diet and Nutrition

  1. Eat a Balanced Diet:
  • Focus on a diet rich in fruits,…
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Added by Mahatma Gandhi Cancer Hospital on November 29, 2024 at 11:59pm — No Comments

CDSCO Import License Consultant for Medical Devices

Introduction to CDSCO Import Licensing for Medical Devices in India

When it comes to importing medical devices into India, the Central Drugs Standard Control Organisation (CDSCO) is the key regulatory authority. Every medical device entering the Indian market must comply with the regulations set by CDSCO, ensuring the safety and efficacy of the product. CDSCO is responsible for setting the standards for drugs and medical devices…

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Added by Indiaxis on May 3, 2024 at 7:44am — No Comments

Know more about Wearable Medical Devices | Operon Strategist

The medical device industry changes constantly as new innovations and advancements are made in development, medical IT, and healthcare. Our medical device blog features expertise from the Sterling Medical Devices team and the latest information and regulation changes in the medical device industry that you should be aware of.

The healthcare and wellness industry is shifting toward regulated, personalized,…

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Added by Neha on October 18, 2022 at 2:41am — No Comments

What is the UKCA Mark for Medical Device?

UKCA stands for United Kingdom Conformity Assessed, and is applied to products placed on the market in the UK. This replaces the CE mark, which – pending changes to legislation - is recognised in the UK until the 30th June 2023. So from this date onwards, medical device manufacturers need to comply with the new UKCA marking regulations.

manufacturers now need to plan for how they will obtain a UK Conformity…

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Added by Neha on October 18, 2022 at 2:40am — No Comments

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