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Amendments_in_EPR_Authorization_For__Electronic_Waste_Corpseed.webp
Amendments in EPR Authorization for Electronic Waste
by Parul Bohral on 2025-11-07

EPR Authorization is an official approval issued by the Central Pollution Control Board (CPCB). It offers producers, importers, and brand owners the legal approval to handle electronic waste generated from their products, right from collection to safe recycling.

MNRE_Issues_SOP_for_ALMM-Wind_and_ALMM-WTC_Enlistment_Process_Corpseed.webp
MNRE Issues SOP for ALMM-Wind and ALMM-WTC Enlistment Process
by Parul Bohral on 2025-11-05

The Approved List of Models and Manufacturers (ALMM) for Wind Turbines and Wind Turbine Components is a quality assurance initiative by the Ministry of New and Renewable Energy (MNRE).

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What Is BIS Certification Under Scheme X? A Complete Overview for Manufacturers
by Parul Bohral on 2025-11-03

Manufacturing in India is evolving fast. But staying compliant with safety and quality standards is not optional, it’s essential. The Bureau of Indian Standards (BIS) ensures that every product made, sold, or imported into India meets strict safety and performance standards.

EPR_Authorization_Amendment_Corpseed.webp
EPR Authorization Amendment: Step-by-Step Overview
by Parul Bohral on 2025-10-31

An EPR Authorization Amendment is an official modification made to an existing EPR certificate issued by the Central Pollution Control Board (CPCB).

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List of Standards Published under Medical Equipment and Hospital Planning (MHD) of BIS- 2025
by Parul Bohral on 2025-10-29

Medical technology and hospital infrastructure significantly shape the way modern healthcare operates today. To ensure the safety, reliability, and quality of medical devices, the Bureau of Indian Standards (BIS) established the Medical Equipment and Hospital Planning Division (MHD).

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What Indian Wholesalers & Retailers Should Know About Exporting FDA-Regulated Pharmaceuticals and Medical Devices to the U.S.
by Parul Bohral on 2025-10-27

India is a significant exporter of pharmaceuticals and medical devices worldwide, with the U.S. being a crucial marketplace. For wholesalers and retailers, exporting to the U.S. can be profitable, but it requires strict adherence to FDA regulations.