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Development_of_Pipeline_Infrastructure_(DPI)_for_Compressed_Biogas_(CBG)_Corpseed.webp
Scheme Guideline for Development of Pipeline Infrastructure (DPI) for Compressed Biogas (CBG) Offtake
by Mahek Sancheti on 2025-09-22

The Development of Pipeline Infrastructure (DPI) scheme sets clear rules to connect Compressed Biogas (CBG) plants with City Gas Distribution (CGD) networks and national gas pipelines.

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How to Prepare PSARA MoU for License Approval?
by Parul Bohral on 2025-09-22

A PSARA MoU is a mandatory requirement for Private Security Agencies (PSA) to obtain a PSARA license. It highlights the responsibility of the training institution to provide comprehensive training to the agency's security personnel.

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Financial Assistance Scheme for Persons with Benchmark Disabilities Having High Support Needs
by Mahek Sancheti on 2025-09-20

The Financial Assistance Scheme for Persons with Benchmark Disabilities having High Support Needs is a welfare program launched in Delhi to extend monthly financial support. It provides an allowance to persons who hold a benchmark disability certificate and are assessed to have high support needs.

MOEF_Import_of_Battery_Lead_Scrap_Rules_Corpseed.webp
MOEF Import of Battery Lead Scrap Rules and Approval in India
by Parul Bohral on 2025-09-20

To import battery lead scrap into India, business need to obtain MOEF clearance. With rising demand for lead scrap, its import is also increasing due to its requirement in automobiles, renewable energy and manufacturing.

What_is_FSSAI_License_Modification_Corpseed.webp
What is FSSAI License Modification? Process, Fee, and Documents Explained
by Parul Bohral on 2025-09-19

FSSAI license is the first and most crucial step for food businesses in India. It ensures that businesses meet basic hygiene standards under the Food Safety and Standard Authority.

Plant_Master_File_for_Medical_Device_Registration_in_India_Corpseed.webp
What is a Plant Master File for Medical Device Registration in India?
by Mahek Sancheti on 2025-09-18

The Plant Master File (PMF) is a detailed document submitted for medical device registration, which describes the manufacturing facility, infrastructure, processes, and quality systems.