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Four years following the procedure, the pocket depths remained in the normal range, the gingiva appeared healthy, and no bleeding was present. Figure 7.

3 renders the sequence patentable 6 and defines that invention through what are known as "functional claims." 7 The question of "inventiveness" might be understood as being linked to the "discovery" of that use. 8 As Recital 23 of the Biotechnology Directive 9 explicitly states: Whereas a mere DNA sequence without indication of a function does not contain any technical information and is therefore not a patentable invention. The European Patent Convention and the European Biotechnology Directive require that the use or industrial application is disclosed in the patent application. This might include the function performed by that sequence or the protein produced 10 but not a merely predicted function 11 ; , which would then be relevant to understanding potential therapeutic or diagnostic uses. 12 In other words, the patent relates to the function rather than the structure of the sequence the identification of an application and use rather than the mere information. The human effort or intervention in an otherwise natural substance and thus, unpatentable subject matter ; is deemed to be found in the technical change that is brought about by the otherwise discovery of the gene sequence and its function. Change is thus invention. Investment can thus be inventive. The concern among commentators on the patentability of gene sequences is that this interpretation of patent protection is not necessarily compatible with the nature of technological innovation in genetic research. In particular, as the law is currently applied, identification of a use for a gene sequence will be sufficient to render the subject matter patentable, but the patent will grant control over all uses of the patented sequence. 13 Therefore, whatever conceptualisation of the actor in which the original rights must vest whether it is the skill and labour of the inventor of the investment of the entrepreneur.
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Deciding when to detoxify someone is important because detoxification without adequate aftercare in place is less likely to lead to sustained abstinence. As stated, an increasing number of detoxifications are associated with increasingly severe withdrawal states and, in addition, the patient's self-efficacy decreases. Community-based detoxification is now common and can be delivered in the home or from a service centre. Generally, the model involves daily contact with a nurse to assess withdrawal and monitor for complications, with prescribing from either the general practitioner or psychiatric or addiction team. There is wide variation in the availability of inpatient facilities for alcohol detoxification, making it hard to be prescriptive about who needs admission, but those with previous severe complications e.g. fits, DTs ; , who are medically or psychiatrically unwell, live alone, with poor support and have previously failed, should be considered for inpatient detoxification. Treatment regimens Several meta-analyses and systematic reviews have concluded that.
Even then, your doctor will closely monitor your health in use of them.

42-47. "The presence of a dependent claim that adds a particular limitation gives rise to a presumption that the limitation in question is not present in the independent claim." Phillips, 415 F.3d at 1315. Furthermore, independent claims are generally given broader scope so as to avoid rendering corresponding dependent claims redundant. Id. at 1324 citing Dow Chem. Co. v. United States, 226 F.3d 1334, 1341 Fed. Cir. 2000 . Therefore, the language of the claims and the doctrine of claim differentiation imply that the "pharmaceutically acceptable polymer" limitation in claim 1 is most likely broader than the "hydrophilic water-soluble polymer" limitation described in claim 2 and involves more compounds than those contained in claim 3. When the claim does not define a term, a court will turn to the specification. The claims " `must be read in view of the specification, of which they are a part, .' because "it is the single best guide to the meaning of a disputed term." Phillips, 415 F.3d at 1315 citing Vitronics, 90 F.3d at 1582 ; . Here, the patent specification provides as follows: The pharmaceutically acceptable polymer is a water-soluble hydrophilic polymer selected from the group consisting of polyvinylpyrrolidine, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, methyl cellulose, vinyl acetate crotonic acid copolymers, methacrylic acid copolymers, maleic anhydride methyl vinyl ether copolymers and derivatives and mixtures thereof. Preferably, the polymer is selected from hydroxypropyl cellulose, hydroxypropylmethyl cellulose, and methyl cellulose. More preferably, the polymer is hydroxypropylmethyl cellulose. Most preferably, the polymer is a low viscosity hydroxypropylmethyl cellulose with viscosity ranging from about 50 cps to about 200 cps. The most preferred low viscosity polymer is a hydroxypropylmethyl cellulose with a viscosity of about 100 cps, commercially available under the Tradename MethocelTM K 100 LV from The Dow Chemical Company.