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Revised_List_of_Activities_under_Article_6.2_Mechanism_of_the_Paris_Agreement.webp
Revised List of Activities under Article 6.2 Mechanism of the Paris Agreement
by Parul Bohral on 2025-09-30

India revises the list of activities under Article 6.2 of the Paris Agreement to support bilateral cooperation, clean technology transfer, and sustainable growth.

Transboundary_Movement_Certificate__and__Waste_Management_Rules_Corpseed.webp
Transboundary Movement Certificate and Waste Management Rules
by Parul Bohral on 2025-09-29

The Transboundary Movement Certificate regulates cross-border waste trade, ensuring safe handling of hazardous materials, legal compliance, and environmental protection.

Import_of_New_Lead_Acid_Battery_in_India__Corpseed.webp
Import of New Lead Acid Battery in India | License, HS Code, and Policy
by Parul Bohral on 2025-09-26

With the rising demand for reliable energy storage, the import of new lead-acid batteries in India is rapidly increasing. These batteries support industrial and domestic requirements, from cars to solar storage and telecom systems, these batteries back up millions of applications.

MoEFCC_Clarifies_EC_Norms_for_Construction_Sector_Corpseed.webp
MoEFCC Clarifies EC Norms for Construction Sector
by Parul Bohral on 2025-09-25

The Ministry of Environment, Forest, and Climate Change (MoEFCC) has issued a significant clarification that will impact the building and construction sector.

Telecommunication_Service_Authorisation_Rules_in_India_Corpseed.webp
Telecommunication Service Authorisation Rules in India
by Parul Bohral on 2025-09-24

Telecommunications play a crucial role in India's economic development and daily life. From mobile calls to internet services, telecom networks connect millions of people in urban and rural areas.

Device_Master_File_in_Medical_Device_Manufacturing_Registration_Corpseed.webp
What is a Device Master File in Medical Device Manufacturing Registration?
by Mahek Sancheti on 2025-09-23

A Device Master File (DMF) is a detailed document used in the medical device industry. It provides complete information about a medical device, covering its design, specifications, manufacturing process, safety measures, and quality checks.