agileregualtory

agileregualtory

Open post's tab

PRGI Registration: A Complete Guide for Businesses
In today’s fast-growing business environment, regulatory compliance plays a crucial role in ensuring smooth operations. One such essential requirement for companies in certain sectors is PRGI registration. PRGI, which stands for “Product Registration for Global Imports”, is a regulatory framework designed to ensure that imported products meet national safety and quality...

83
agileregualtory

Open post's tab

WPC Import License – A Complete Guide for Importers in India
A WPC Import License is a mandatory approval issued by the Wireless Planning & Coordination (WPC) Wing of the Ministry of Communications, Government of India. This license is required for importing wireless and radio frequency–based products into India that operate on specific frequency bands. Devices such as Bluetooth gadgets, Wi-Fi routers, wireless keyboards, smart devices, IoT...

88
agileregualtory

Open post's tab

CDSCO Registration – A Complete Guide for Medical and Pharmaceutical Businesses
CDSCO Registration is a mandatory regulatory requirement for companies involved in the manufacturing, import, distribution, and sale of drugs, cosmetics, medical devices, and diagnostics in India. CDSCO stands for the Central Drugs Standard Control Organization, which functions under the Ministry of Health and Family Welfare, Government of India. It acts as the national regulatory authority to...

77
agileregualtory

Open post's tab

EPR Battery Import Registration: A Complete Guide for Compliance in India
Extended Producer Responsibility (EPR) Battery Import Registration is a mandatory regulatory requirement in India for importers of batteries, battery packs, and battery-operated equipment. Introduced under the Battery Waste Management Rules, 2022, and enforced by the Central Pollution Control Board (CPCB), EPR ensures that producers and importers take responsibility for the environmentally...

104
agileregualtory

Open post's tab

Revised Schedule M in Pharmacy
Schedule M of the Drugs and Cosmetics Rules, 1945, is a crucial regulatory framework that outlines the Good Manufacturing Practices (GMP) required for pharmaceutical manufacturing in India. The revised Schedule M represents a significant step forward in aligning India’s pharmaceutical manufacturing standards with global quality expectations, particularly those of the World Health...

85
agileregualtory

Open post's tab

ISI Mark: Ensuring Quality, Safety, and Trust in Indian Products
The ISI Mark is one of the most recognized symbols of quality and safety in India. Issued by the Bureau of Indian Standards (BIS), the ISI Mark certifies that a product complies with the Indian Standards specified for that particular product. Introduced in 1955, the ISI certification scheme plays a crucial role in protecting consumers and ensuring that manufacturers adhere to established...

92
agileregualtory

Open post's tab

Drug License – A Legal Requirement for Pharmaceutical Businesses
A Drug License is a mandatory legal authorization required to manufacture, distribute, sell, stock, or import drugs and pharmaceuticals in India. Issued under the Drugs and Cosmetics Act, 1940, and Rules, 1945, this license ensures that medicines available in the market are safe, effective, and of standard quality. Any individual or business involved in the pharmaceutical supply chain must...

83
agileregualtory

Open post's tab

To Start a Newspaper in India
Starting a newspaper in India is an ambitious and rewarding venture that combines journalism, business strategy, and regulatory compliance. With India’s vast and diverse readership, newspapers continue to play an important role in informing the public, shaping opinions, and strengthening democracy. However, launching a newspaper requires careful planning, legal approvals, and a clear...

92
agileregualtory

Open post's tab

Medical Oxygen Manufacturing Plant: Setup, Process, and Regulatory Overview
A medical oxygen manufacturing plant plays a critical role in the healthcare infrastructure by producing high-purity oxygen used in hospitals, clinics, and emergency care facilities. Medical oxygen is essential for patient respiratory support, anesthesia, intensive care units, and various therapeutic applications. Establishing a medical oxygen plant requires careful planning, technical...

86
agileregualtory

Open post's tab

Pharmacy License in Delhi: A Complete Guide
A pharmacy license in Delhi is a mandatory legal requirement for anyone intending to open or operate a medical store, wholesale drug business, or online pharmacy within the National Capital Territory. Regulated under the Drugs and Cosmetics Act, 1940 and Drugs Rules, 1945, the license ensures that medicines are stored, sold, and distributed safely and responsibly. Without a valid...

69
agileregualtory

Open post's tab

CPCB EPR Credit: A Key Pillar of India’s Waste Management Framework
The concept of CPCB EPR Credit has emerged as a cornerstone of India’s Extended Producer Responsibility (EPR) framework, designed to strengthen sustainable waste management practices. Governed by the Central Pollution Control Board (CPCB), EPR credits provide a structured, transparent mechanism for ensuring that producers, importers, and brand owners (PIBOs) take...

92
agileregualtory

Open post's tab

WPC Import License: A Complete Guide
The WPC Import License is a mandatory authorization required for importing wireless and radio frequency (RF) devices into India. Issued by the Wireless Planning & Coordination (WPC) Wing under the Ministry of Communications, this license ensures that imported wireless equipment complies with India’s frequency and safety regulations. Any device that operates on...

94