Chapter III contains requirements for the labelling and instructions for use of IVDs. The basis of all chapters and requirements is the intended purpose and the associated risk classification. The intended purpose of the IH-IVD influences the effort required to implement the three central elements ...
2.Without prejudice to the application of other Community provisions on the classification, packaging and labelling of substances, suppliers shall ensure before the placing on the market that the packaging of aerosol dispensers referred to above is marked visibly, legibly and indelibly with: "For ...
INFORMAS Protocol: Food Labelling Module - Annex 3: Photographic methods for measuring packaged food and beverage products in Supermarkets.Canter, RebeccaReyes, MarcelaCoravalan, CamilaKanter, R.; Reyes, M.; Corvalan, C. Photographic Methods for Measuri...
labelling of dangerous substances and preparations, the placing on the market and use of these fibres and of articles containing these fibres, as permitted according to the preceding derogations, shall be permitted only if the articles bear a label in accordance with the provisions of Appendix 7...
For example, presentation, packaging, labelling, patient information leaflet, batch number, expiry date should the need arise during the shelf life of the batch concerned. There may be exceptional circumstances where this requirement can be met without retention of duplicate samples e.g. where small...
13. Describe your procedures for control of packaging and labelling operations for end products 14. Describe your procedurefor maintenance of equipment and calibration of instruments 15. Are the employees regularly trained and is the training documented? 16. Describe the type of general GMP training ...
REACH物质宣告_ANNEXXVII.PDF,11Fl., No. 205, Sec. 3, Beishin Rd., Xindian Dist., New Taipei City 231, Taiwan, R.O.C. TEL: +886-2-8913-1588 FAX: +886-2-8913-1788 Web: REACH regulation compliance _ ANNEX XVI REACH 物質宣告_ANNEX XVII The list of restriction
2.1.5Labellinginformation101 2.2Conditionstobefulfilled101 2.3Documentationrequired102 3.Glossary102 4.Administrativechanges104 1.Changeinthenameand/orcorporateaddressofthesupplieroftheFPP104 2.ChangeinthenameoraddressofamanufacturerofanAPIthatisnotasupplier ...
nal contai ner and labelling. An FPP may co 36、ntain one or more APIs.gap analysisIdenti? cati on of cri tical elements of a process which are available at the SU but are missing from the RU.good manufacturing practices (GMP)That part of qual ity assurance which ensures that pharmace...
4.3.6 Weights and balances 砝码和天平 (13)4.3.7 Volumetric equipment 测定体积的设备 (13)4.3.8 Other equipment 其他设备 (13)5. Reagents and culture media 试剂和培养基 (14)5.1 Reagents 试剂 (14)5.2 Media 培养基 (14)5.3 Labelling 贴签 (16)5.4 Organism resuscitation 微生物复苏 (...