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Foreigner registration is a mandatory requirement by the Government of India under which all foreign nationals (excluding overseas citizens of India) visiting India on a long term visa (more than 180 days) are required to register themselves with a Registration Officer within 14 days of arriving in India. [2]
On 30 November 2016 the Government of India approved further liberalization, simplification and rationalization of visa regime in India. It also announced that more countries would be added to the e-visa list. [80] The e-visa would have a validity of 60 days and could be applied for by foreign nationals up to four months ahead of the visit. [81]
The late fee is to be paid by physically going to the State Bank of India, with the late fee payment details form. The State Bank of India is a state run bank. To deposit the money you will need, A photocopy of the payment details form obtained from the Foreigners Regional Registration Office. 1,400 rupees in cash.
Visa requirement to visit India Angola: Visa not required for 30 days e-Visa Barbados: Visa not required for 90 days e-Visa Bolivia: Visa on arrival for 90 days, charged at La Paz airport. Prior visa is free of cost at Bolivian embassy. e-Visa for 60 days Burundi: Visa on Arrival for 30 days e-Visa Cambodia: Visa on arrival for 30 days
It serves a similar function to the Food and Drug Administration (FDA) of the United States or the European Medicines Agency of the European Union. The Indian government has announced its plan to bring all medical devices, including implants and contraceptives under a review of the Central Drugs and Standard Control Organisation (CDSCO).
The Food Safety and Standards Authority of India (FSSAI) is a statutory body under the administration of the Ministry of Health and Family Welfare, Government of India. It regulates the manufacture, storage, distribution, sale, and import of food articles, while also establishing standards to ensure food safety . [ 4 ]
The Common Technical Document (CTD) is a set of specifications for an application dossier for the registration of medicine, designed for use across Europe, Japan, the United States, and beyond. [ 1 ] Major Synopsis
The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.