Corpseed provides a variety of services centered on compliance, business registration, certification, and environmental regulatory obligations. Key offerings include:
Company incorporation/startup business plans / intellectual property services (as per their “who we are” story).
Company incorporation/startup business plans / intellectual property services (as per their “who we are” story).
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14/10/1955
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Obtain WPC NOC Certificate for Importers & Manufacturers
https://medium.com/@dsouzaemily64/wpc-noc-certificate-for-importers-manufacturers-in-india-e3534727a27f?postPublishedType=initial
India has seen a large increase in the number of wireless and smart devices. Because of this increase, importers & manufacturers of electronic products with Radio-Frequency (RF)-enabled technologies must comply with the regulatory requirements for compliance in India. The Wireless Planning & Coordination (WPC) Wing, which operates as part of the Ministry of Communications, is responsible for issuing one of these important approvals, the WPC Certificate for Importers & Manufacturers of India.
#wirelessdevices
#legal
#certificate
#license
#registrationObtain WPC NOC Certificate for Importers & Manufacturers https://medium.com/@dsouzaemily64/wpc-noc-certificate-for-importers-manufacturers-in-india-e3534727a27f?postPublishedType=initial India has seen a large increase in the number of wireless and smart devices. Because of this increase, importers & manufacturers of electronic products with Radio-Frequency (RF)-enabled technologies must comply with the regulatory requirements for compliance in India. The Wireless Planning & Coordination (WPC) Wing, which operates as part of the Ministry of Communications, is responsible for issuing one of these important approvals, the WPC Certificate for Importers & Manufacturers of India. #wirelessdevices #legal #certificate #license #registration0 Yorumlar 0 hisse senetleri 49 Views 0 önizleme -
Know About the CDSCO Product Approval Process
https://www.prbusinesswires.com/CDSCO-Product-Approval-Process
Manufacturers, importers, and distributors intending to commercialize regulated products on the Indian market should comply with the CDSCO's product registration regulations and obtain CDSCO registration through the official registration procedure under the Medical Device Rules 2017.
#cdscoregistration
#medicaldevice
#productregistrationKnow About the CDSCO Product Approval Process https://www.prbusinesswires.com/CDSCO-Product-Approval-Process Manufacturers, importers, and distributors intending to commercialize regulated products on the Indian market should comply with the CDSCO's product registration regulations and obtain CDSCO registration through the official registration procedure under the Medical Device Rules 2017. #cdscoregistration #medicaldevice #productregistration0 Yorumlar 0 hisse senetleri 360 Views 0 önizleme -
Obtain BIS CRS Registration for Notebook Computers
https://corpseed5.wordpress.com/2025/12/09/documents-required-for-bis-crs-registration-for-notebook-computers/
In India, the increasing trend of notebook computer demand is increasing because of digitalization, remote working and e-learning. The Bureau of Indian Standards (BIS) has required that notebook computers be registered under its Compulsory Registration Scheme (CRS), which was set up by the Ministry of Electronics and Information Technology (MeitY), to ensure a safe and high-quality experience for all users.
#biscrsregistration
#legal
#compliance
#bureauofindianstandardsObtain BIS CRS Registration for Notebook Computers https://corpseed5.wordpress.com/2025/12/09/documents-required-for-bis-crs-registration-for-notebook-computers/ In India, the increasing trend of notebook computer demand is increasing because of digitalization, remote working and e-learning. The Bureau of Indian Standards (BIS) has required that notebook computers be registered under its Compulsory Registration Scheme (CRS), which was set up by the Ministry of Electronics and Information Technology (MeitY), to ensure a safe and high-quality experience for all users. #biscrsregistration #legal #compliance #bureauofindianstandards0 Yorumlar 0 hisse senetleri 212 Views 0 önizleme -
FDA Approval Process for Drugs & Medical Devices
https://dsouzaemily64.wixsite.com/my-site-2/post/fda-approval-process-for-drugs-medical-devices-a-full-roadmap
A long and difficult process to bring a new drug or medical device onto the market includes safety testing, clinical testing, scientific evaluation, as well as government approval of the drug or medical device. In the United States of America, the Food and Drug Administration (FDA) is the agency responsible for approving drugs and medical devices before consumers can use them legally.
#foodandrugs
#fdaaproval
#license
#registrationFDA Approval Process for Drugs & Medical Devices https://dsouzaemily64.wixsite.com/my-site-2/post/fda-approval-process-for-drugs-medical-devices-a-full-roadmap A long and difficult process to bring a new drug or medical device onto the market includes safety testing, clinical testing, scientific evaluation, as well as government approval of the drug or medical device. In the United States of America, the Food and Drug Administration (FDA) is the agency responsible for approving drugs and medical devices before consumers can use them legally. #foodandrugs #fdaaproval #license #registration0 Yorumlar 0 hisse senetleri 310 Views 0 önizleme -
Apply for Factory License in Maharashtra
https://www.articleswebhunk.in/how-to-apply-for-factory-license-maharashtra-certificate/
Applying for a Factory License in Maharashtra is now simple with expert guidance. The license is mandatory for all manufacturing units operating under the Factories Act, 1948. To apply, businesses must submit documents such as building plan approval, machinery details, worker information, safety measures, and statutory compliance reports.
#factorylicense
#factoriesact
#business
#legal
#factoryregistrationApply for Factory License in Maharashtra https://www.articleswebhunk.in/how-to-apply-for-factory-license-maharashtra-certificate/ Applying for a Factory License in Maharashtra is now simple with expert guidance. The license is mandatory for all manufacturing units operating under the Factories Act, 1948. To apply, businesses must submit documents such as building plan approval, machinery details, worker information, safety measures, and statutory compliance reports. #factorylicense #factoriesact #business #legal #factoryregistration0 Yorumlar 0 hisse senetleri 263 Views 0 önizleme -
Rule 27 of the Legal Metrology Act
https://worldwidedigest.com/why-rule-27-of-legal-metrology-act-matters-for-manufacturers/
Rule 27 of the Legal Metrology (Packaged Commodities) Rules, 2011 mandates that every manufacturer, packer, or importer of pre-packaged commodities must register with the Legal Metrology Department. This registration ensures that all packaged goods sold in India follow the required labeling, quantity, and declaration standards.
#legalmetrology
#certificate
#registration
#packagedcommoditiesRule 27 of the Legal Metrology Act https://worldwidedigest.com/why-rule-27-of-legal-metrology-act-matters-for-manufacturers/ Rule 27 of the Legal Metrology (Packaged Commodities) Rules, 2011 mandates that every manufacturer, packer, or importer of pre-packaged commodities must register with the Legal Metrology Department. This registration ensures that all packaged goods sold in India follow the required labeling, quantity, and declaration standards. #legalmetrology #certificate #registration #packagedcommodities0 Yorumlar 0 hisse senetleri 191 Views 0 önizleme -
Obtain an FDA License for Perfume
https://blogosm.com/fda-license-for-perfume
The Rapid Growth of the Perfume and Fragrance Industry in India requires all manufacturers and sellers to obtain the appropriate FDA License(s) before selling their products legally.
#fdalicense
#perfumeindustry
#business
#registration
#legalObtain an FDA License for Perfume https://blogosm.com/fda-license-for-perfume The Rapid Growth of the Perfume and Fragrance Industry in India requires all manufacturers and sellers to obtain the appropriate FDA License(s) before selling their products legally. #fdalicense #perfumeindustry #business #registration #legal0 Yorumlar 0 hisse senetleri 205 Views 0 önizleme -
Top Benefits of BIS CCTV Registration in India
https://dsouzaemily64.wixsite.com/my-site-2/post/top-benefits-of-bis-cctv-registration-in-india
The surveillance and security market in India is expanding rapidly. To sell their products in India, CCTV manufacturers must adhere to certain mandatory quality standards. One of the most important compliance requirements for CCTV manufacturers is that they must have a BIS CCTV Registration.
#cctvregistration
#bisregistration
#legal
#businessTop Benefits of BIS CCTV Registration in India https://dsouzaemily64.wixsite.com/my-site-2/post/top-benefits-of-bis-cctv-registration-in-india The surveillance and security market in India is expanding rapidly. To sell their products in India, CCTV manufacturers must adhere to certain mandatory quality standards. One of the most important compliance requirements for CCTV manufacturers is that they must have a BIS CCTV Registration. #cctvregistration #bisregistration #legal #business0 Yorumlar 0 hisse senetleri 87 Views 0 önizleme -
SCOMET License Consultant
https://www.articleswebhunk.in/scomet-license-consultant-quick-guide-to-requirements/
Items that are either special or sensitive and are exported from India need strict adherence to government rules to make sure of the nation’s security and safety on the global front. And one of the important requirements is the SCOMET License, which is issued by the Directorate General of Foreign Trade (DGFT).
#scometlicense
#registration
#certificate
#importexportSCOMET License Consultant https://www.articleswebhunk.in/scomet-license-consultant-quick-guide-to-requirements/ Items that are either special or sensitive and are exported from India need strict adherence to government rules to make sure of the nation’s security and safety on the global front. And one of the important requirements is the SCOMET License, which is issued by the Directorate General of Foreign Trade (DGFT). #scometlicense #registration #certificate #importexport0 Yorumlar 0 hisse senetleri 141 Views 0 önizleme -
Download PESO Certificate Sample: Eligibility, Process & Checklist
https://corpseed5.wordpress.com/2025/11/25/download-peso-certificate-sample-eligibility-process-checklist/
In order to operate with industrial equipment, gas cylinders, pressure vessels, and explosive materials, it is critical that you possess the appropriate compliance documentation as a business in India, and one of the essential approvals required is a PESO Certificate.
#pesocertificate
#registration
#license
#petroleumDownload PESO Certificate Sample: Eligibility, Process & Checklist https://corpseed5.wordpress.com/2025/11/25/download-peso-certificate-sample-eligibility-process-checklist/ In order to operate with industrial equipment, gas cylinders, pressure vessels, and explosive materials, it is critical that you possess the appropriate compliance documentation as a business in India, and one of the essential approvals required is a PESO Certificate. #pesocertificate #registration #license #petroleum0 Yorumlar 0 hisse senetleri 207 Views 0 önizleme -
Choosing the Right CDSCO Registration Consultant: What You Must Know
https://blogosm.com/cdsco-registration-consultant
In India, compliance plays a crucial role in the medical device and pharmaceutical industries. The Central Drugs Standard Control Organization (CDSCO) is the national regulatory authority responsible for approving, monitoring, and regulating medical devices and drugs. Whether you're a manufacturer, importer, or distributor, obtaining a CDSCO registration is mandatory before launching your product in the Indian market.
#cdsco
#medicaldevice
#registration
#certificateChoosing the Right CDSCO Registration Consultant: What You Must Know https://blogosm.com/cdsco-registration-consultant In India, compliance plays a crucial role in the medical device and pharmaceutical industries. The Central Drugs Standard Control Organization (CDSCO) is the national regulatory authority responsible for approving, monitoring, and regulating medical devices and drugs. Whether you're a manufacturer, importer, or distributor, obtaining a CDSCO registration is mandatory before launching your product in the Indian market. #cdsco #medicaldevice #registration #certificate0 Yorumlar 0 hisse senetleri 191 Views 0 önizleme -
Obtain DMF Compliance for Medical Devices with Corpseed Experts
https://www.corpseed.com/service/cdsco-device-master-file-dmf
Having a compliant and full Device Master File (DMF) is the first step in ensuring your medical device meets regulatory compliance. Corpseed helps manufacturers complete, review, and submit DMF documentation all at once—all to get into the market faster.
Our professionals will prepare your DMF using everything from technical documents to a risk profile, to a quality system, which ensures compliance with the requirements and expectations of CDSCO, ISO, and global regulatory frameworks.
With Corpseed, you get:
✔ End-to-end DMF preparation
✔ Professional regulatory guidance
✔ Error-free documentation
✔ Quicker delivery and compliance
#devicemasterfile
#medicaldevice
#registrationObtain DMF Compliance for Medical Devices with Corpseed Experts https://www.corpseed.com/service/cdsco-device-master-file-dmf Having a compliant and full Device Master File (DMF) is the first step in ensuring your medical device meets regulatory compliance. Corpseed helps manufacturers complete, review, and submit DMF documentation all at once—all to get into the market faster. Our professionals will prepare your DMF using everything from technical documents to a risk profile, to a quality system, which ensures compliance with the requirements and expectations of CDSCO, ISO, and global regulatory frameworks. With Corpseed, you get: ✔ End-to-end DMF preparation ✔ Professional regulatory guidance ✔ Error-free documentation ✔ Quicker delivery and compliance #devicemasterfile #medicaldevice #registration0 Yorumlar 0 hisse senetleri 291 Views 0 önizleme
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