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Authorised Version

ECHA (2011) Guidance on the preparation of an application for authorisation. Version 1. ECHA-ll-G-Ol-EN... [Pg.542]

The worker in gold was an important member of the community hq is mentioned in Nehemiah iii. 8 by name, along with the apothecary and, indeed, given pride of place before him. Gold was worked in various ways it was refined in furnaces (Prov. xvii. 3), cast (Exod. xxxii. 4) and beaten into plates — the goldbeater being referred to as the carpenter in the Authorised Version. [Pg.128]

Such documents and their associated technologies, written for and about the teacher, construct authorised versions of the curriculum subject, teacher and student. These statements officially write the teacher and the student - who they should be, what they are to do and say and when and how they must do... [Pg.119]

See MW, vii i5o, where Bunyan remarks that in some of your old Bibles, that which in one place is called a Target, in another is called, a Shield . In 2 Chronicles 14 8, the Geneva Bible has shields where the Authorised Version has targets . For the reference to Tyndale, see MW, xii 27, 426n. [Pg.52]

The Apocrypha was included in the Geneva Bible and in the Authorised Version in the seventeenth century, and indeed right up until the 18 20s, when the British and Foreign Bible Society decided to exclude it from all the editions it distributed, and it came to be omitted more generally. [Pg.52]

A document control function is required to regulate the authorisation and circulation of such documents. This involves the sign-off on a master copy of the document by authorized personnel, followed by a recorded circulation of official copies to relevant departments. If a document needs to be updated, the revised version should be reviewed and approved by the same functions that approved the original. The revised version is then issued with a new version number and date, and all copies of the obsolete version should be destroyed other than the obsolete master, which may be kept for historical traceability. [Pg.24]

It is then necessary to review the meaning of special needs. It is difficult to see how such needs can exist where there is a licensed version of the product on the market for the physician to use. However tempting it may be for medical institutions to save costs by requesting an unlicensed version of a licensed product, economic needs will never be special needs in this context. This accords with the rationale underlying the Directive, which requires only authorised medicinal products to be placed on the market unless exceptional circumstances apply. [Pg.385]

Following Edward Jenner s discovery of a smallpox vaccine in 1798, and the demonstration by Benjamin Waterhouse in the United States in 1800 that the vaccine was effective, fraudulent versions of the vaccine were marketed throughout the country. A Baltimore physician, John Smith, initially convinced the Maryland legislature to enact a statute designed to ensure the availability of an effective smallpox vaccine supply, and then persuaded Congress to enact the Vaccine Act of 1813 - for the same purpose. This statute authorised the President to appoint a federal agent to preserve the genuine vaccine matter and to furnish the same to any citizen who requested it. [Pg.567]

UK Draft TGD, Concerning the placing of biocidal products on the market Common principles and practical procedures for the authorisation and registration of products Version 4, May 1998. [Pg.118]

Advertising to healthcare professionals for a specific medicinal product can be started only after it has received marketing authorisation from Swissmedic. The statements made when advertising to healthcare professionals must concur with the currently valid version of the approved professional information. Printed advertising (advertisements, pamphlets, brochures, etc.) to healthcare professionals must be easily legible in respect of font size and layout. [Pg.157]

Whereas agreements on patents and authorised production can be negotiated in cases of shortages (see section on shortages), this has so far not yet been possible in cases of national versus pharmaceutical industry interests on behalf of neglected patients. Patented medicines block the production of more affordable generic versions while more and more patients become sick or die because the medicines they need to stay alive are simply too expensive. Recently, much attention has been attracted by India s efforts to increase access to medicines and implement a patent system... [Pg.39]

A SOP bears a date, usually the date of authorisation, in combination with a version number. Whenever changes in a SOP are made, the version number is incremented. [Pg.733]


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