How Long Does CPCB Take to Approve EPR Applications?

The CPCB typically takes 15 to 60 working days to approve EPR applications submitted on the CPCB EPR Portal. The timeline depends on the type of waste (plastic, e-waste, battery, etc.) and the accuracy of the documents submitted. Delays may occur if the application is incomplete or if CPCB seeks clarification. Submitting correct documents in the right format helps speed up the process. If you're facing delays or unsure about the process, consider expert help.

Agile Regulatory offers end-to-end support for EPR registration and approval.
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PHARMEXCIL Registration – Mandatory for Pharma Exporters in India

Description :
PHARMEXCIL (Pharmaceuticals Export Promotion Council of India) registration is essential for Indian pharmaceutical companies planning to export their products globally. It provides exporters with access to various government incentives, international trade fairs, and global networking opportunities under the Ministry of Commerce. The registration also enables exporters to obtain the RCMC (Registration-cum-Membership Certificate) which is mandatory for availing export benefits under the Foreign Trade Policy. If you're new to the process, getting expert help can save you time and prevent errors. Agile Regulatory offers complete assistance for PHARMEXCIL registration, including document preparation, portal submission, and liaison with council officials. Their team ensures smooth approval, helping your pharma business stay export-ready and compliant.

Register here - https://www.agileregulatory.co....m/service/pharmexcil

How to Register Under the Bed and Breakfast Scheme in India

Description :
The Bed and Breakfast Scheme was introduced by the Ministry of Tourism to promote affordable and homely accommodation for both domestic and international tourists. Under this scheme, homeowners can legally rent out rooms in their residences to travelers, provided they meet the required standards and amenities. Registration under the scheme requires submitting an application along with documents such as ID proof, property ownership papers, photographs of the rooms, and a police clearance certificate. The classification is typically into “Gold” or “Silver” categories based on facilities offered. If you're planning to monetize extra space in your home or operate a small hospitality setup, registering under this scheme is highly beneficial. At Agile Regulatory, we offer expert assistance for Bed and Breakfast registration—including documentation, eligibility checks, form submissions, and coordination with tourism departments. We ensure that your registration process is smooth and legally compliant so that you can start hosting with confidence.


Register here - https://www.agileregulatory.co....m/service/bed-and-br

Difference Between Retail and Wholesale Drug License in India?

The main difference between a retail and wholesale drug license in India lies in the nature of the business operations. A retail drug license is issued to pharmacies or chemist shops that sell medicines directly to consumers, typically requiring the presence of a registered pharmacist. In contrast, a wholesale drug license permits the sale of drugs in bulk to retailers, hospitals, or other licensed entities, and does not always require a pharmacist on-site but does require qualified personnel with experience in pharmaceuticals. Both licenses are issued under the Drugs and Cosmetics Act, and understanding their specific criteria is essential before starting a medical business.

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CE Mark Certification – Ensure Product Access to European Market

CE Mark Certification is essential for manufacturers who want to sell their products in the European Economic Area (EEA). It indicates that your product meets EU safety, health, and environmental protection requirements. Whether you're exporting electronics, machinery, medical devices, or toys, obtaining a CE mark is a mandatory step for market access.

Agile Regulatory offers end-to-end assistance in CE Certification, helping businesses understand applicable EU directives, prepare technical documentation, and coordinate with notified bodies (if required). Our experts guide you through conformity assessment procedures and Declaration of Conformity preparation, ensuring your product is fully compliant and ready for international trade. We’ve helped multiple Indian manufacturers navigate complex CE marking requirements smoothly and quickly. If you're planning to expand to Europe, connect with Agile Regulatory for professional support with CE Mark Certification.

Register here - https://www.agileregulatory.co....m/service/ce-mark-ce