DIN ISO 11418-7-2017 Containers and accessories for pharmaceutical preparations - Part 7 Screw-neck vials made of glass tubing for liquid dosage forms (ISO 11418-7 2016)《药品配制用容器及附件.pdf
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1、February 2017 English price group 7No part of this translation may be reproduced without prior permission ofDIN Deutsches Institut fr Normung e. V., Berlin. Beuth Verlag GmbH, 10772 Berlin, Germany,has the exclusive right of sale for German Standards (DIN-Normen).ICS 11.040.20; 11.120.99!%_z“2608799
2、www.din.deDIN ISO 11418-7Containers and accessories for pharmaceutical preparations Part 7: Screwneck vials made of glass tubing for liquid dosage forms (ISO 114187:2016),English translation of DIN ISO 11418-7:2017-02Behltnisse und Zubehr fr Arzneimittel Teil 7: Gewindeflaschen aus Rhrenglas fr flss
3、ige Arzneimittel (ISO 114187:2016),Englische bersetzung von DIN ISO 11418-7:2017-02Rcipients et accessoires pour prparations pharmaceutiques Partie 7: Flacons avec bague vis en verre tir pour diagnostics forme liquide (ISO 114187:2016),Traduction anglaise de DIN ISO 11418-7:2017-02SupersedesDIN ISO
4、114187:199901www.beuth.deDocument comprises 9 pagesDTranslation by DIN-Sprachendienst.In case of doubt, the German-language original shall be considered authoritative.01.17 A comma is used as the decimal marker. National Annex NA (informative) Bibliography 4Introduction . 51 Scope . 62 Normative ref
5、erences 63 Dimensions and designation . 63.1 Dimensions . 63.2 Designation 64 Material 75 Characteristics 86 Requirements 86.1 Hydrolytic resistance . 86.2 Annealing quality 86.3 Light resistance 87 Marking 88 Packaging . 8Contents PageDIN ISO 11418-7:2017-02 2National foreword .3National foreword T
6、his document (ISO 11418-7:2016) has been prepared by Technical Committee ISO/TC 76 “Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use“ with the active participation of German experts. The responsible German body involved in its preparation was DIN
7、-Normenausschuss Medizin (DIN Standards Committee Medicine), Working Committee NA 063-02-03 AA Verpackungssysteme fr die Befllung und Applikation von medizinischen Produkten. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. DIN sha
8、ll not be held responsible for identifying any or all such patent rights. The DIN ISO 11418 series consists of the following parts, under the general title Containers and accessories for pharmaceutical preparations: Part 1: Drop-dispensing glass bottles Part 2: Screw-neck glass bottles for syrups Pa
9、rt 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms Part 4: Tablet glass bottles Part 5: Dropper assemblies Part 7: Screw-neck vials made of glass tubing for liquid dosage forms The DIN Standards corresponding to the International Standards referred to in this document are as fo
10、llows: ISO 719 DIN ISO 719 ISO 720 DIN ISO 720 ISO 4802-1 DIN ISO 4802-1 ISO 4802-2 DIN ISO 4802-2 Amendments This standard differs from DIN ISO 11418-7:1999-01 as follows: a) in Table 1, the mass of screw-neck vials has been updated; b) the text of the standard has been editorially revised. Previou
11、s editions DIN 58378-1: 1983-08 DIN ISO 11418-7: 1999-01 DIN ISO 11418-7:2017-02 3 National Annex NA (informative) Bibliography DIN ISO 719, Glass Hydrolytic resistance of glass grains at 98 C Method of test and classification DIN ISO 720, Glass Hydrolytic resistance of glass grains at 121 C Method
12、of test and classification DIN ISO 4802-1, Glassware Hydrolytic resistance of the interior surfaces of glass containers Part 1: Determination by titration method and classification DIN ISO 4802-2, Glassware Hydrolytic resistance of the interior surfaces of glass containers Part 2: Determination by f
13、lame spectrometry and classification DIN ISO 11418-7:2017-02 4 IntroductionThe purpose of this part of ISO 11418 is to specify the dimensions, capacities, form and requirements of screw-neck vials made from tubular glass intended for medical use. Vials made from glass tubing are considered to be sui
14、table for the packaging and storage of pharmaceutical preparations until they are administered for medicinal purposes. Such vials may be made of different types of glass which can affect chemical resistance properties. For example, those made from borosilicate glass will have a very high level of ch
15、emical resistance where others made from soda-lime-silica glass will have a lower but adequate chemical resistance for the purposes for which they are intended.Because vials may be made from different types of glass and because it is the chemical behaviour of the internal surface which is important
16、when they are filled with pharmaceutical preparations, it is essential to specify the test procedures by which the performance can be measured.DIN ISO 11418-7:2017-02 5 Containers and accessories for pharmaceutical preparations Part 7: Screw-neck vials made of glass tubing for liquid dosage forms1 S
17、copeThis part of ISO 11418 specifies the design, dimensions, material and requirements of screw-neck vials for pharmaceutical preparations. Screw-neck vials are applicable to primary packs used in direct contact with a drug.This part of ISO 11418 applies to colourless or amber glass vials made from
18、borosilicate or soda-lime-silica glass, made from glass tubing and intended to be used in the packaging, storage or transportation of pharmaceutical products.NOTE The potency, purity, stability and safety of a drug during its manufacture and storage can be strongly affected by the nature and perform
19、ance of the primary pack.2 Normative referencesThe following documents, in whole or in part, are normatively referenced in this document and are indispensable for its application. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced docum
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