A drug license is an official permission granted to individuals or companies that manufacture, distribute, and sell drugs in India. It ensures adherence to the safety and quality standards of the regulatory authorities that ensure public health.

The importation of cosmetics in India is governed by the Drugs and Cosmetics Act, of 1940. Form 42 is the application for a registration certificate, hence safety standards are ensured. Form 43 is the actual certificate of registration issued post-approval.

CDSCO online registration is a process that ensures that all the drugs, medical devices, and cosmetics in the market are safe, reliable, and must have passed quality standards. Importers, manufacturers, and others must register under the CDSCO for a certificate if they are working in this field.

A free sale certificate is a document required in a certain country for certain material such as Medical Devices, food items, cosmetics, and biological products.

The Certificate of Pharmaceutical Products or COPP is the core document in the pharmaceutical industry. It is a required instrument for international trade and regulatory compliance. This document is issued by any country's regulatory authority upon request from a product owner.

Obtaining an FDA wholesale license is a must for traders involved in selling or distributing food and medicine in bulk. It assures that safety standards are followed. The license safeguards consumer health and builds trust among them. Owning an official authorization also helps avoid fines or any legal issues. Without a valid FDA license, businesses are not allowed to trade.

The CDSCO is responsible for medical device registration in India. This registration guarantees that all devices are safe, of high quality, and comply with regulatory standards. This registration not only protects patients but also supports global trade.

Clinical trials can assist doctors in determining if the risks of a new treatment are acceptable when compared to the possible benefits. The outcomes of clinical trials are unknown to researchers.

Obtaining a Homeopathy Drug License is a lengthy process that necessitates the submission of numerous documents and papers. Let's take a closer look at the prerequisites.

Applicants requesting authorization to conduct BA/BE studies with various pharmacological dose formulations on Indian subjects have been submitting applications to the office of the Drugs Controller General (India) at CDSCO (HQ) FDA Bhawan in New Delhi.

If you are manufacturing pharmaceutical products and want to expand your reach to the global market, get the ADC NOC (No-Objection Certificate from Assistant Drug Controller) and other drug export-related consultations from Corpseed.

If your business requires any kind of drug (except for medicinal use) to operate then you need to get the Dual Use NOC from the zonal office of the CDSCO. Corpseed can assist you to get this NOC and mitigate any possible hurdle that may arise in the process.

Obtaining an ISO 14971 certification can enhance career prospects by equipping professionals with specialized skills and expanding their possibilities in the medical device sector.

The CDSCO Registration process for the Import of Cosmetics is mandatory as it provides several advantages as working under legal terms and conditions, it ensures product quality it builds trust among the consumers, etc.

Getting a cosmetic import license or a manufacturing license for cosmetics in India is not an option it’s a legal obligation for an importer planning to import cosmetic goods in the Indian market. Every business that wants to sell, import, or make cosmetics must get a drug and cosmetic license to stay compliant and keep products safe for consumers.

The beauty industry is a sector of manufacturing that directly affects the health of consumers. Consumers are generally concerned about the quality and safety of the cosmetics they use, as these products come in direct contact.

ISO 13485 Certification is an international standard for the quality and safety of medical devices. It helps manufacturers, importers, and others who need this to meet customer requirements and follow regulatory standards properly.

A CDSCO test license allows the import or manufacture of small quantities of drugs for research, testing, or analysis. It ensures pharmaceutical safety, compliance, and product evaluation under the Drugs and Cosmetics Act before large-scale production or market release.

The Device Master File supports the safe entry of medical devices into the market. It stores complete design, testing, labelling, and risk data. The CDSCO Device Master File helps meet regulatory standards and demonstrates that the device functions safely and effectively.

A Plant Master File (PMF) explains how a medical device manufacturing plant works in real life. It proves safe production, strong quality control, and compliance with the CDSCO guidelines under the Medical Devices Rules (MDR) 2017. The plant master file for medical device registration in India ensures that only high-quality devices reach hospitals, clinics, and patients.

A loan license for drug manufacturing allows a business to manufacture drugs at another approved factory. The licensed factory must follow drug rules, quality control, and record maintenance. The authority checks all conditions before issuing the license for listed products and operations.

A loan license for medical devices allows a company to manufacture devices using another licensed factory's facility. It supports startups and small companies in entering the medical device market by using approved infrastructure while meeting safety and quality standards under CDSCO rules.

A loan license for cosmetic manufacturing allows a brand to produce cosmetic products in a licensed factory. It helps cosmetic businesses enter the market more quickly and stay compliant with the Drugs and Cosmetics Act, 1940, and the Cosmetics Rules.

CDSCO Market Standing Certificate proves valid manufacturing licenses and active sales in India. It enhances credibility, supports tender participation, and aids foreign registration of products. The MSC certificate strengthens the company's reputation and ensures regulatory compliance for medical devices.

Importing medical devices in India needs detailed paperwork and clear compliance. The CDSCO Form MD-26 is the legal way for importers to get approval to import medical devices intro the country. An appropriate MD-26 makes customs clearance simpler and keeps your devices legally permitted in India. If you are an importer, distributor, or foreign manufacturer working with an Indian agent, understanding MD-26 and its necessities is crucial to prevent delays, rejections, or regulatory issues.

Non-notified medical device registration in India allows new medical products to enter the Indian market safely and legally. This registration ensures that every device is checked for quality before it reaches hospitals or clinics. The Central Drugs Standard Control Organisation (CDSCO) reviews and approves each device through a clear and structured process, making sure it meets all the safety and performance standards in India.

The CDSCO Non-Conviction Certificate confirms that a medical device company has a clean legal record without any conviction under the Drugs and Cosmetics Act. It supports trust, safety, and compliance in the medical device industry. It also helps companies take part in tenders, approvals, and public procurement activities in India.

Importing Indian medical devices requires strict regulatory approvals to ensure patient safety and product quality. The CDSCO MD 16 license is a crucial permit that allows businesses to import approved medical devices legally and confidently. Without this license, no importer can bring medical devices into India.

A loan license allows a business without its own factory to manufacture products through an approved unit legally. It ensures safe, compliant, and regulated production in pharma, cosmetics, and medical devices. This licensing model supports quality control, legal authorization, and smooth market entry for highly regulated sectors.

Obtaining RCMC registration through the Export Promotion Council for Medical Devices is essential for exporters aiming for legal recognition and access to DGFT benefits. This registration ensures eligibility for government incentives and also provides a clear framework to support structured growth in the medical device export sector.

CDSCO Non-Sterile Non-Measuring medical device registration permits the lawful sale of low-risk medical devices in India. It includes only Class A medical devices under Medical Device Rules, 2017. The SLA is the authority who issues NSNM certificate for manufacturers and importers.

BIS CRS inclusion is essential when manufacturers launch or add new models under an existing BIS registration. Without appropriate inclusion approval, even allowed products can go through sales blocks, customs issues, or regulatory action in India.