BS ISO 11418-3-2016 Containers and accessories for pharmaceutical preparations Screw-neck glass bottles (veral) for solid and liquid dosage forms《药剂制备容器及附件 固体和液体计量方式螺口玻璃瓶》.pdf
《BS ISO 11418-3-2016 Containers and accessories for pharmaceutical preparations Screw-neck glass bottles (veral) for solid and liquid dosage forms《药剂制备容器及附件 固体和液体计量方式螺口玻璃瓶》.pdf》由会员分享,可在线阅读,更多相关《BS ISO 11418-3-2016 Containers and accessories for pharmaceutical preparations Screw-neck glass bottles (veral) for solid and liquid dosage forms《药剂制备容器及附件 固体和液体计量方式螺口玻璃瓶》.pdf(16页珍藏版)》请在麦多课文档分享上搜索。
1、BS ISO 11418-3:2016Containers and accessories for pharmaceutical preparationsPart 3: Screw-neck glass bottles (veral) for solid and liquid dosage formsBSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06BS ISO 11418-3:2016 BRITISH STANDARDNational forewordThis British St
2、andard is the UK implementation of ISO 11418-3:2016. It supersedes BS ISO 11418-3:2005 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/212, IVDs.A list of organizations represented on this committee can be obtained on request to its secretary.This p
3、ublication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2016.Published by BSI Standards Limited 2016ISBN 978 0 580 88425 2 ICS 11.040.20; 11.120.99 Compliance with a British Standard canno
4、t confer immunity from legal obligations.This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 November 2016.Amendments/corrigenda issued since publicationDate T e x t a f f e c t e dBS ISO 11418-3:2016 ISO 2016Containers and accessories for pha
5、rmaceutical preparations Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage formsRcipients et accessoires pour prparations pharmaceutiques Partie 3: Flacons en verre bouchon vis (veral) pour formes sches et liquidesINTERNATIONAL STANDARDISO11418-3Third edition2016-11-15Reference nu
6、mberISO 11418-3:2016(E)BS ISO 11418-3:2016ISO 11418-3:2016(E)ii ISO 2016 All rights reservedCOPYRIGHT PROTECTED DOCUMENT ISO 2016, Published in SwitzerlandAll rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized otherwise in any form or by any means,
7、 electronic or mechanical, including photocopying, or posting on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address below or ISOs member body in the country of the requester.ISO copyright officeCh. de Blandonnet 8 CP 401CH-1214 V
8、ernier, Geneva, SwitzerlandTel. +41 22 749 01 11Fax +41 22 749 09 47copyrightiso.orgwww.iso.orgBS ISO 11418-3:2016ISO 11418-3:2016(E)Foreword iv1 Scope . 12 Normative references 13 Terms and definitions . 14 Dimensions and designation . 24.1 Dimensions . 24.2 Designation 25 Requirements 25.1 Materia
9、l . 25.2 Performance 25.2.1 Vertical load resistance 25.2.2 Hydrolytic resistance . 25.2.3 Thermal shock resistance 26 Marking 2Annex A (normative) Neck finishes . 5 ISO 2016 All rights reserved iiiContents PageBS ISO 11418-3:2016ISO 11418-3:2016(E)ForewordISO (the International Organization for Sta
10、ndardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the righ
11、t to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.The procedures
12、used to develop this document and those intended for its further maintenance are described in the ISO/IEC Directives, Part 1. In particular the different approval criteria needed for the different types of ISO documents should be noted. This document was drafted in accordance with the editorial rule
13、s of the ISO/IEC Directives, Part 2 (see www.iso.org/directives).Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of any patent rights identif
14、ied during the development of the document will be in the Introduction and/or on the ISO list of patent declarations received (see www.iso.org/patents).Any trade name used in this document is information given for the convenience of users and does not constitute an endorsement.For an explanation on
15、the meaning of ISO specific terms and expressions related to conformity assessment, as well as information about ISOs adherence to the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see the following URL: www.iso.org/iso/foreword.html.The committee responsible for
16、 this document is ISO/TC 76, Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use.This third edition cancels and replaces the second edition (ISO 11418-3:2005), which has been technically revised by updating Figure 1 on typical screw-neck glass bottl
17、e and Table 1 on nominal volume, brimful capacity and dimensions of screw-neck glass bottles, including a normative annex on neck finishes, and editorially revising this document.A list of all the parts of ISO 11418 can be found on the ISO website.iv ISO 2016 All rights reservedBS ISO 11418-3:2016IN
18、TERNATIONAL STANDARD ISO 11418-3:2016(E)Containers and accessories for pharmaceutical preparations Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms1 ScopeThis document specifies the design, dimensions, material and requirements of screw-neck glass bottles (veral) for pharma
19、ceutical preparations in solid and liquid dosage forms. Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.This document is applicable to screw-neck glass bottles (veral) used in pharmacy. Together with the corresponding closure systems, they serve for packag
20、ing of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.NOTE The potency, purity, stability and safety of a drug during its manufacture and storage can be strongly affected by the nature and performance of the primary pack.2 Normative referencesT
21、he following documents are referred to in the text in such a way that some or all of their content constitutes requirements of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies
22、.ISO 719, Glass Hydrolytic resistance of glass grains at 98 degrees C Method of test and classificationISO 720, Glass Hydrolytic resistance of glass grains at 121 degrees C Method of test and classificationISO 1101, Geometrical product specifications (GPS) Geometrical tolerancing Tolerances of form,
23、 orientation, location and run-outISO 4802-1, Glassware Hydrolytic resistance of the interior surfaces of glass containers Part 1: Determination by titration method and classificationISO 4802-2, Glassware Hydrolytic resistance of the interior surfaces of glass containers Part 2: Determination by fla
24、me spectrometry and classificationISO 7459, Glass containers Thermal shock resistance and thermal shock endurance Test methodsISO 8113, Glass containers Resistance to vertical load Test method3 Terms and definitionsNo terms and definitions are listed in this document.ISO and IEC maintain terminologi
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