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The National Institute of Informatics (国立情報学研究所, Kokuritsu Jōhōgaku Kenkyūjo, NII) is a Japanese research institute located in Chiyoda, Tokyo, Japan.NII was established in April 2000 for the purpose of advancing the study of informatics.
Voluntary registration available for computer programs and databases. [37] South Africa: Companies and Intellectual Property Commission (CIPC) Voluntary registration available for cinematograph films. Establishes prima facie evidence of the facts contained on the registration certificate and may be used in court as proof of those facts. [38] Spain
This law removed the requirement that a second term of copyright protection is contingent on a renewal registration. The effect was that any work copyrighted in the US in 1964 or after had a copyright term of 75 years, whether or not a formal copyright renewal was filed. There are some legal reasons for filing such renewal registrations.
The Information Technology Act, 2000 defines Critical Information Infrastructure (CII) as “… those computer resource, the incapacitation or destruction of which, shall have debilitating impact on national security, economy, public health or safety".
The authority for this type of registration is set forth in the Lanham Act, which permits concurrent use registration where the concurrent use applicant made a good-faith adoption of the mark prior to the registrant filing an application for registration. Such registrations are most commonly achieved by agreement of the parties involved ...
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Cancer centers must renew their status with the NIH every 5 years. The NIH funds cancer centers through a P30 Cancer Center Support Grant (CCSG) mechanism. [2] To be eligible to apply, a cancer center must receive at least $10 million in cancer research funding annually. Preparation for these grant applications can be extensive.
In most countries, a marketing authorisation is valid for a period of 5 years. After this period, one should apply for renewal of the marketing authorisation, usually by providing minimal data proving that quality, efficacy and safety characteristics are maintained and the risk-benefit ratio of the medicinal product is still favourable.