Purification Sample Clauses

Purification the purification brought about by removing 80 per cent of the impurity content or the reduction or elimination that produces a chemical with a minimum degree of purity to make the product suitable for uses such as:

Purification. 2.3.1 Issuance of the agreement giving legal form to and formalizing the ad hoc Commission: A+5. 2.3.2 Establishment of the ad hoc Commission: D+105. 2.3.3 Result of the evaluation: D+195. 2.3.4 Corresponding administrative decisions: D+225. 2.3.5 Implementation: D+255.

Purification. A good shall be considered satisfying the purification rule and shall be treated as an originating good provided that one of the following occurs in the territory of the Party: (a) the elimination of not less than 80 percent of the content of existing impurities; or (b) the reduction or elimination of impurities resulting in a good suitable for one or more of the following applications: (i) as a pharmaceutical, medicinal, cosmetic, veterinary, or food grade substances; (ii) as a chemical products or reagents for analytical, diagnostic, or laboratory uses; (iii) as elements or components for use in micro-elements; (iv) for specialized optical uses; (v) for non-toxic uses for health and safety; (vi) for biotechnical use; (vii) as carriers used in a separation process; or (viii) for nuclear grade uses. A good of Chapters 30, 31, 33 through 38 except for heading 38.08, shall be treated as an originating good if the deliberate and proportionally controlled mixing or blending (including dispersing) of materials to conform to predetermined specifications, resulting in the production of a good having physical or chemical characteristics that are relevant to the purposes or uses of the good and are different from the input materials, occurs in the territory of the Party.

Purification. The Parties agree to a process of purification of the armed forces, within the framework of the peace process and with a view to the supreme objective of national reconciliation, based on evaluation of all members of the armed forces by an ad hoc Commission. A. The evaluation shall take into account the past performance of each officer, including, in particular: (1) his record of observance of the legal order, with particular emphasis on respect for human rights, both in his personal conduct and in the rigour with which he has ordered the redress and punishment of unlawful acts, excesses or human rights violations committed under his command, especially if there have been serious or systematic omissions in the latter respect;

Purification. A A A z∈Z A A t,x,z | − | | − | | − | | ≥ | A. Achievability proof ∈ ∈ ≤ ∈ − → → ∞ B. Converse proof B E E m ,m L n n , Γ , Ξ → ∞ ≤ n n n n n ω⊗ n ABE .

Purification. 2.1. List of raw materials and specifications (e.g. resin identification, column loads) 2.2. Process Protocols for the current purification process (e.g. buffer recipes, cleaning protocols) 2.3. Historical process data (e.g. yields, reproducibility, clearance of contaminants, product aggregate) 2.4. Data on product stability, especially at intermediate hold points 2.5. Reference Antibody1 for assay development and comparability studies

Purification purification that eliminates eighty per cent (80%) of existing impurities or the reduction or elimination produced by a chemical substance with a minimum degree of purity, so that the product may be appropriate for uses such as: a) pharmaceutical substances or food products that meet national or international pharmacopoeial standards; b) reactive chemical products for chemical analysis or for laboratory use; c) elements and components for use in microelectronics; d) various optical applications; e) human or veterinary use. 4 The use of non-originating oil base under heading 27.10 will be allowed for the production of “lubricating oils”.

Purification. With isolated crude Moli1901, generated at Apotex Fermentation Inc., the purification process supplied by Molichem Medicines will be verified in the chemistry lab.

Purification. All compounds delivered to Pfizer will be purified via at least one of the following methods 1) *, 2) * or 3) *. The purity of the final compounds must be determined as detailed in section above. On rare occasions, and only with the agreement of Pfizer, the * and not the * compounds will be purified, however the purity of the * compounds delivered to Pfizer must still be determined and meet the above purity criteria.