LICENSE REQUIREMENT OF TRADING OF OXYGEN CYLINDER
The availability of drugs and medicines is important in ensuring the good health of the Nation. However, the availability of drugs and medicines should be prevented to ensure that those goods are not abused or abused by people. Therefore, the government has set strict rules and regulations for the production and distribution of drugs and drugs in India. The regulation governing the manufacture and sale of drugs is provided by the Drugs and Cosmetics Act, 1940, and the laws enacted under it. Control for drug use from the category of non-flammable substances during manufacture, sale, distribution, and time transferred to a patient or consumer by a pharmacist at a retail store, hospital, or pharmacy. In 1964, Ayurvedic and Unani drugs were also incorporated under the Drugs and Cosmetics Act, 1940. However, some businesses may require different types of drug licenses based on their business.
Under the Drugs and Cosmetics Act, the regulation of the manufacture, sale, and distribution of drugs is primarily a concern of State authorities while the Central Authorities oversee the licensing of New Drugs, Clinical Trials in the country, setting drug policies, controlling imported drugs, integration of Drug Enforcement Services and of the Drug and Cosmetics Act. The Director of General Drugs in India is responsible for approving licenses for certain categories of drugs. The Central Government in exercising its powers under Sections 5 and 7 of the Act stated that the prescribed regulations namely the Gas Cylinder Rules, 2004 regulate the filling, ownership, transport, and importation of such gases. The purpose of these Regulations is to ensure the safety of the majority of persons involved in the filling, ownership, transport, and importation of such gases.
MANUFACTURING PRACTICE FOR MEDICAL GASES
The organization must be a manufacturer of Medical Gases namely Medical oxygen IP, Nitrous oxide IP, Medical carbon dioxide, IP and must have a valid production license issued from