License, defined

Open source technologies offer dynamic applications for real estate tailored to meet business development needs. Open source tools are usually available at no charge under a license defined by the Open Source Initiative. Open source tools may be viable alternatives to popular closed-source applications, and some open source tools offer features or performance benefits that surpass their commercial counterparts. The term open source tools is synonymous with open source utility and similar to open source applications. 

Specifications for hGH products are defined by the governmental licensing authorities, eg, the U.S. Pood and Dmg Administration. Draft monographs for hGH have been prepared by both the EnitedStates Pharmacopia and the European Pharmacopeia commissions and should be formally adopted by 1995. These specifications are suitable for biosynthetic hGH. The much less purified pituitary-derived hGH has virtually disappeared from commercial production. An international reference standard for pituitary-derived hGH (lot 80/505) has been used for caUbration, particularly for bioassay purposes. A highly purified biosynthetic hGH standard (lot 88/624) has been prepared and should be formally adopted by 1995, or before. 

The licensing process consists of two steps construction and operating license that must be completed before fuel loading. Licensing covers radiological safety, environmental protection, and antitru,st considerations. Activities not defined as production or utilization of special nuclear material (SNM), use simple one-step. Materials Licenses, for the possession of radioactive materials. Examples are uranium mills, solution recovery plants, UO fabrication plants, interim spent fuel storage, and isotopic separation plants. 

In the near future new drugs for the treatment of Alzheimer s disease are expected to be licensed, and it would be extremely valuable to be able to compare them in a clear and well-defined framework. In addition, if economic evaluation is to inform health and social care providers and policy-makers about the potential impact of new interventions in practice, estimation of the value for money of these new interventions requires consideration of (a) the perceived and objective risks and benefits of care (b) attitudes of people with... 

See also CFR Web site, http //www.access.gpo.gov/nara/cfr/index.html. An August 1997 guideline, Post-Marketing Adverse Experience Reporting for Human Drug and Licensed Biological Products Clarification of What to Report, defined the minimum data relevant for a safety report as... 

The definitions provided above underscore the importance of understanding and interpreting prescriptions. A prescription is defined as an order for medication from a doctor, dentist, veterinarian, or any other licensed health care professional authorized to prescribe in that state. It shows the relationship between the prescriber, patient, and the pharmacist, in which the latter provides the medication to the patient. 

LICENSEE.— The term licensee means a licensed importer (as defined in section 921(a)(9) of tide 18, United States Code), a licensed manufacturer (as defined in section 921(a)(10) of that tide), or a licensed dealer (as defined in section 921(a)(ll) of that title). 

The dataset used in this example comprised two phase III placebo-controlled studies used in the license application for oseltamivir (Tamiflu ). See Patel, Kay and Rowell (2006) for further details. Pre-defined symptoms consisted of cough, nasal congestion, headache, sore throat, fatigue, myalgia and feverishness and each of these was assessed on an ordinal scale none, mild, moderate, severe. Alleviation was recorded as the day on which all symptoms... 

Parts 210 and 211 of CFR Title 21 are the laws defining good manufacturing practices for finished pharmaceutical products. All manufacturers must follow these regulations in order to market their products in the United States. When a firm files an application to market a product in the United States through a New Drug Application (NDA), abbreviated NDA, (ANDA), Biological License Application (BLA),... 

Durham-Humphrey Act(1952) - This amendment defined specific drugs which may be supplied by a licensed pharmacist upon the prescription by a registered physician. Under this act these drug prescriptions may not be refilled unless authorized by the physician. 

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