[{"data":1,"prerenderedAt":807},["ShallowReactive",2],{"page-\u002Fzh-hans\u002Fguides\u002Fpharmaceutical-packaging":3,"related-\u002Fzh-hans\u002Fguides\u002Fpharmaceutical-packaging":787},{"id":4,"title":5,"author":6,"body":7,"category":6,"description":773,"extension":774,"heading":775,"heroImage":6,"heroImageAlt":6,"layout":776,"meta":777,"navigation":778,"ogImage":779,"path":780,"publishedAt":781,"sections":6,"seo":782,"sourcePath":783,"stem":784,"updatedAt":785,"videos":6,"__hash__":786},"pages\u002Fzh-hans\u002Fguides\u002Fpharmaceutical-packaging.md","医药包装：全球标准与本地法规",null,{"type":8,"value":9,"toc":709},"minimark",[10],[11,12,13,17,20,23,26,29,38,41,57,62,65,68,71,78,81,86,89,94,97,102,105,110,113,122,125,128,133,136,141,144,149,152,161,164,167,173,176,181,184,189,192,197,200,209,212,215,220,223,229,232,237,240,250,253,256,259,264,267,272,275,280,283,288,291,296,299,308,313,316,321,324,329,332,337,340,345,348,351,354,376,385,388,391,396,399,404,407,412,415,418,422,425,431,438,445,452,459,462,465,468,471,491,494,497,523,526,529,549,558,561,564,584,587,590,610,613,616,636,639,642,662,665,668,688,697,700,703,706],"div",{},[14,15,16],"p",{},"医药包装在制药行业中扮演着至关重要的角色，确保药品的安全性、有效性与合规性。它不仅仅是打造一个吸引人的外观，更在于融入各种关键要素，以保护药物、向消费者提供必要信息，并满足严格的监管标准。医药包装的复杂性源于需要在功能性与合规性、安全性和产品完整性之间取得平衡。",[14,18,19],{},"制药行业受到严格监管，而包装是药物递送系统的关键组成部分。从所用材料的类型到展示的信息，每一个细节都必须符合全球监管机构设定的特定标准。这些标准确保包装能够保护药物免受环境因素影响，为患者和医疗专业人员提供清晰的说明和警示，并有助于防止假冒和滥用。",[14,21,22],{},"医药包装的全球标准包括来自美国食品药品监督管理局（FDA）、欧盟欧洲药品管理局（EMA）以及其他国家监管机构的指南。这些标准通常要求标注药物名称、剂量、活性成分、批号、有效期和储存条件等信息，所有这些对于确保安全和药效都至关重要。",[14,24,25],{},"本地法规又增加了一层复杂性。例如，印度要求医药包装上带有 QR 码，这是提升药品可追溯性、防止假冒产品的重要举措。这些 QR 码提供有关药物的详细信息，包括生产日期和有效期、批号等，只需用智能手机扫描即可轻松获取。",[14,27,28],{},"除了满足监管要求，现代医药包装还必须借助技术进步来改善整体供应链和患者体验。带有数字链接的 GS1 2D 条码正是技术如何提升医药包装的绝佳范例。",[14,30,31,32,37],{},"通过采用带有数字链接的 GS1 2D 条码，制药公司和包装解决方案供应商可以显著增强包装的功能性和安全性。",[33,34,36],"a",{"href":35},"\u002F","Digital Link"," 等提供的解决方案为实施这类先进条码提供了强大工具，确保无缝集成和全面的数据管理。",[14,39,40],{},"总而言之，医药包装是一门多层面的学科，需要深入理解监管要求、技术进步和市场需求。本指南旨在全面概述医药包装的关键要素，帮助行业专业人士驾驭其中的复杂性，确保产品安全、有效且合规。",[42,43,44],"figure",{},[45,46,47,50],"picture",{},[48,49],"source",{},[51,52],"img",{"alt":53,"height":54,"src":55,"width":56},"医药包装是一门多层面的学科",441,"\u002Fimages\u002F2024\u002F07\u002Fpharmaceutical-packaging-is-a-multifaceted-discipline.jpg",728,[58,59,61],"h2",{"id":60},"什么是医药包装","什么是医药包装？",[14,63,64],{},"医药包装涉及从生产环节到最终用户，用于容纳和保护药品的各种流程、材料和技术。",[14,66,67],{},"它是制药行业的一个关键方面，确保药品安全、有效并能送达患者手中。医药包装涵盖一系列组成部分，各自承担特定功能，以满足监管要求、维护产品完整性并支持患者遵从用药。",[58,69,70],{"id":70},"医药包装的功能",[72,73,75],"h3",{"id":74},"保护",[76,77,74],"strong",{},[14,79,80],{},"医药包装的首要功能是保护药品免受物理损坏和光照、湿气、氧气、污染等环境因素的影响。这确保药物在整个保质期内始终有效且安全可用。",[72,82,84],{"id":83},"信息",[76,85,83],{},[14,87,88],{},"包装是患者、医疗专业人员和监管机构的重要信息来源。它包含药物名称、用药说明、活性成分、批号、有效期、生产商信息和储存条件等关键细节。这些信息对于正确用药和确保安全至关重要。",[72,90,92],{"id":91},"合规与监管",[76,93,91],{},[14,95,96],{},"医药包装必须符合 FDA、EMA 及其他国家机构等监管部门设定的严格要求。这些法规确保包装具有防拆封特征，在必要时具备防儿童开启功能，并正确标注所有必需信息。",[72,98,100],{"id":99},"便利与遵从",[76,101,99],{},[14,103,104],{},"包装会显著影响患者对用药方案的遵从度。易于开启的容器、清晰的标签以及便捷的剂型（如泡罩包装或预充式注射器）等特征，有助于患者正确、持续地服药。",[72,106,108],{"id":107},"营销与品牌",[76,109,107],{},[14,111,112],{},"包装在药品的营销和品牌塑造中也发挥着作用。它有助于将不同产品区分开来，并能传达品牌的重要方面，如质量和可靠性。",[42,114,115],{},[45,116,117,119],{},[48,118],{},[51,120],{"alt":70,"height":54,"src":121,"width":56},"\u002Fimages\u002F2024\u002F07\u002FFunctions-of-pharmaceutical-packaging.jpg",[58,123,124],{"id":124},"医药包装的组成部分",[14,126,127],{},"医药包装通常分为三种主要类型。",[72,129,131],{"id":130},"一级包装",[76,132,130],{},[14,134,135],{},"这是与药品直接接触的包装，包括泡罩包装、瓶子、小瓶、安瓿和预充式注射器等。一级材料必须为惰性材料，不与药物发生相互作用。它们构成抵御污染和降解的第一道防线。",[72,137,139],{"id":138},"二级包装",[76,140,138],{},[14,142,143],{},"这是容纳一级包装的包装，例如盒子、纸箱和外包装。二级包装在运输和储存过程中提供额外保护，通常还包含有关药物的重要信息。",[72,145,147],{"id":146},"三级包装",[76,148,146],{},[14,150,151],{},"三级包装包括用于批量装卸和分销的板条箱、托盘和大型容器。它确保大量药品能够安全、高效地运输。",[42,153,154],{},[45,155,156,158],{},[48,157],{},[51,159],{"alt":124,"height":54,"src":160,"width":56},"\u002Fimages\u002F2024\u002F07\u002FComponents-of-pharmaceutical-packaging.jpg",[58,162,163],{"id":163},"制药行业的监管要求",[14,165,166],{},"医药包装须遵守旨在确保药品安全性和有效性的严格监管要求。这些要求可能因国家而异，但通常包括以下几项。",[168,169,171],"h4",{"id":170},"防拆封特征",[76,172,170],{},[14,174,175],{},"包装必须具备能够明显显示是否被开启或改动过的特征。这有助于防止篡改，并确保药物安全可用。",[168,177,179],{"id":178},"防儿童开启包装",[76,180,178],{},[14,182,183],{},"某些药物必须以儿童难以开启的方式包装，从而降低误食的风险。",[168,185,187],{"id":186},"清晰标注",[76,188,186],{},[14,190,191],{},"标签必须提供有关药物的全面信息，包括名称、规格、用药说明和警示。这有助于确保患者和医疗专业人员正确用药。",[168,193,195],{"id":194},"序列化与可追溯性",[76,196,194],{},[14,198,199],{},"监管机构越来越多地要求药品带有唯一标识（如条码或 QR 码），以便在整个供应链中进行追踪。这有助于防止假药进入市场，并在必要时便于高效召回。",[42,201,202],{},[45,203,204,206],{},[48,205],{},[51,207],{"alt":163,"height":54,"src":208,"width":56},"\u002Fimages\u002F2024\u002F07\u002FRegulatory-requirements-in-the-pharmaceutical-industry.jpg",[58,210,211],{"id":211},"医药包装行业中的技术",[14,213,214],{},"医药包装行业不断发展，新技术持续增强包装的功能性和安全性。一些值得关注的进步包括智能包装解决方案、GS1 2D 条码或数字链接 QR 码，以及更具可持续性的包装材料。",[72,216,218],{"id":217},"智能包装",[76,219,217],{},[14,221,222],{},"融入传感器和指示器等电子元件，以监测药品的状态。例如，温度敏感标签可以显示药物是否曾暴露于推荐范围以外的温度。",[72,224,226],{"id":225},"gs1-2d-条码",[76,227,228],{},"GS1 2D 条码",[14,230,231],{},"这类条码能够存储比传统条码更多的信息，并包含通向全面在线数据的数字链接。它提升了可追溯性和防伪能力，并可即时获取详尽的产品信息。",[72,233,235],{"id":234},"可持续包装",[76,236,234],{},[14,238,239],{},"药品包装行业越来越注重使用环保材料并减少包装废弃物。这包括使用可生物降解材料，以及优化包装设计以尽量减少多余材料。",[42,241,242],{},[45,243,244,246],{},[48,245],{},[51,247],{"alt":211,"height":248,"src":249,"width":56},440,"\u002Fimages\u002F2024\u002F07\u002FTechnology-in-the-pharmaceutical-packaging-industry.jpg",[58,251,252],{"id":252},"制药与包装企业的强制标注信息",[14,254,255],{},"医药包装必须包含特定、详尽的信息，以符合监管要求并确保药品的安全性和有效性。这些强制信息有助于防止用药错误、增强可追溯性，并为患者和医疗专业人员提供必要指导。理解这些要求，对于包装制造商和医药包装市场上的企业满足监管标准、保护公众健康至关重要。",[72,257,258],{"id":258},"强制信息的关键要素",[168,260,262],{"id":261},"药物名称",[76,263,261],{},[14,265,266],{},"包装必须清晰标示药物的通用名和商品名。这有助于避免混淆，对于可能同时服用多种药物的患者尤为重要。",[168,268,270],{"id":269},"用药说明",[76,271,269],{},[14,273,274],{},"精确的用药说明对于确保患者正确服药至关重要，包括推荐剂量、给药频率和给药途径（如口服、注射）。",[168,276,278],{"id":277},"活性成分",[76,279,277],{},[14,281,282],{},"需列出活性成分及其浓度，以告知患者和医疗专业人员该药的成分构成。这对于识别潜在过敏原或与其他药物的相互作用尤为重要。",[168,284,286],{"id":285},"批号",[76,287,285],{},[14,289,290],{},"每件包装都必须包含唯一批号，以便在必要时进行追溯和召回。批号使制造商和监管机构能够追踪生产历史。",[168,292,294],{"id":293},"有效期",[76,295,293],{},[14,297,298],{},"有效期表明药物的保质期，确保患者不会使用超出有效安全期限的产品。该日期对于维持药效和安全至关重要。",[42,300,301],{},[45,302,303,305],{},[48,304],{},[51,306],{"alt":258,"height":248,"src":307,"width":56},"\u002Fimages\u002F2024\u002F07\u002FKey-elements-of-mandatory-information.jpg",[168,309,311],{"id":310},"生产商信息",[76,312,310],{},[14,314,315],{},"包装必须提供有关生产商的详细信息，包括公司名称、地址和联系方式。这可确保问责，并在需要进一步信息或发生不良事件时提供联系途径。",[168,317,319],{"id":318},"储存条件",[76,320,318],{},[14,322,323],{},"具体的储存说明有助于维持药物的稳定性和有效性，可能包括温度要求、避光和湿度控制。",[168,325,327],{"id":326},"安全信息",[76,328,326],{},[14,330,331],{},"安全信息包括对潜在药物不良反应、禁忌症和注意事项的警示。这部分有助于患者和医疗专业人员避免有害影响，安全用药。",[168,333,335],{"id":334},"使用说明",[76,336,334],{},[14,338,339],{},"清晰说明如何使用药物，包括给药前所需的任何准备或操作，对于确保正确使用至关重要。",[168,341,343],{"id":342},"合规标志",[76,344,342],{},[14,346,347],{},"包装必须显示表明符合监管标准的标志或符号，例如欧盟的 CE 标志或美国的 FDA 批准。这些标志向使用者保证产品的安全性和有效性。",[58,349,350],{"id":350},"准确标注的重要性",[14,352,353],{},"准确标注是医药包装制造商的基石，服务于多个关键目的：",[355,356,357,364,370],"ul",{},[358,359,360,363],"li",{},[76,361,362],{},"防止用药错误","：清晰、精确的标注有助于防止药物调配和给药错误，避免造成严重的健康后果。",[358,365,366,369],{},[76,367,368],{},"提升患者安全","：标注提供有关药物、用法和潜在风险的所有必要信息，确保患者安全、有效地用药。",[358,371,372,375],{},[76,373,374],{},"促进合规","：满足监管机构设定的标注要求，可确保制药公司遵守法律，避免处罚或产品召回。",[42,377,378],{},[45,379,380,382],{},[48,381],{},[51,383],{"alt":350,"height":248,"src":384,"width":56},"\u002Fimages\u002F2024\u002F07\u002FImportance-of-accurate-labeling.png",[58,386,387],{"id":387},"本地要求与实例",[14,389,390],{},"不同国家拥有不同的医药市场，对处方药和医药包装也有各自特定的额外要求。",[72,392,394],{"id":393},"美国",[76,395,393],{},[14,397,398],{},"美国食品药品监督管理局（FDA）要求某些药物采用防儿童开启包装，以防止儿童误食，并要求采用清晰的标注体系，为患者和医疗专业人员提供指导。",[72,400,402],{"id":401},"欧盟",[76,403,401],{},[14,405,406],{},"欧盟要求采用防拆封包装，以确保药品的完整性。这包括封条或封带等特征，可清楚显示包装是否被开启或改动过。",[72,408,410],{"id":409},"印度",[76,411,409],{},[14,413,414],{},"印度法规要求在医药包装上加入 QR 码，以增强可追溯性并防止假药。",[14,416,417],{},"这些 QR 码存储有关产品的关键信息，包括生产日期、有效期和批号。",[58,419,421],{"id":420},"gs1-2d-条码在医药包装中的作用","GS1 2D 条码在医药包装中的作用",[14,423,424],{},"带有数字链接的 GS1 2D 条码正在彻底改变医药包装。这类先进条码能够存储比传统线性条码更多的信息，并包含通向全面在线数据的数字链接。",[72,426,428],{"id":427},"gs1-2d-条码的优势",[76,429,430],{},"GS1 2D 条码的优势",[14,432,433,434,437],{},"1. ",[76,435,436],{},"增强可追溯性","：提供从生产到最终用户的详细审计轨迹，这对于召回和监测用药遵从度至关重要。",[14,439,440,441,444],{},"2. ",[76,442,443],{},"防伪","：有助于验证产品的真实性，降低供应链中的假冒风险。",[14,446,447,448,451],{},"3. ",[76,449,450],{},"提升安全性","：患者和医疗专业人员通过扫描条码，即可获取有关药物的最新信息，包括使用说明和潜在副作用。",[14,453,454,458],{},[33,455,456],{"href":35},[76,457,36],{}," 是该领域的领先解决方案，提供强大工具以有效实施 GS1 2D 条码。它通过提供无缝集成和全面的数据管理解决方案，为医药包装市场提供支持。",[58,460,461],{"id":461},"医药包装的步骤",[14,463,464],{},"医药包装是一个复杂的过程，涉及多个关键步骤，以确保药品安全、有效地送达患者。包装过程中的每一步都旨在维护药物的完整性、符合监管要求并支持患者遵从用药。以下是医药包装所涉及关键步骤的详细说明：",[72,466,467],{"id":467},"设计与开发",[14,469,470],{},"医药包装的第一步是设计与开发阶段。这涉及：",[355,472,473,479,485],{},[358,474,475,478],{},[76,476,477],{},"概念构思","：打造既满足功能要求又满足美学要求的包装设计，包括考虑药物类型、目标患者群体和品牌策略。",[358,480,481,484],{},[76,482,483],{},"材料选择","：必须为一级、二级和三级包装选择合适的材料。材料必须与药品相容，并能充分防护环境因素和污染。",[358,486,487,490],{},[76,488,489],{},"合规","：确保包装设计符合 FDA、EMA 及其他相关机构设定的所有监管标准和指南。",[72,492,493],{"id":493},"原型制作与测试",[14,495,496],{},"初步设计完成后，即制作原型并进行严格测试。",[355,498,499,505,511,517],{},[358,500,501,504],{},[76,502,503],{},"原型开发","：根据设计规格制作实体包装样品。",[358,506,507,510],{},[76,508,509],{},"稳定性测试","：评估包装在温度、湿度和光照等各种环境条件下的表现，确保包装能够在整个保质期内保护药物。",[358,512,513,516],{},[76,514,515],{},"相容性测试","：确保包装材料不会与药品产生不良相互作用，从而可能影响其安全性或有效性。",[358,518,519,522],{},[76,520,521],{},"用户测试","：与真实患者和医疗专业人员一起评估包装的易用性，确保其满足需求且易于使用。",[72,524,525],{"id":525},"生产",[14,527,528],{},"在成功完成原型制作和测试后，包装设计进入生产阶段。",[355,530,531,537,543],{},[358,532,533,536],{},[76,534,535],{},"材料采购","：采购生产所需的材料，确保其符合质量标准和监管要求。",[358,538,539,542],{},[76,540,541],{},"生产线搭建","：搭建生产线以制造包装组件，包括配置机械和流程以处理特定的材料和设计特征。",[358,544,545,548],{},[76,546,547],{},"质量控制","：实施严格的质量控制措施，确保一致性并符合设计规格，包括在生产过程中定期检查和测试。",[42,550,551],{},[45,552,553,555],{},[48,554],{},[51,556],{"alt":525,"height":248,"src":557,"width":56},"\u002Fimages\u002F2024\u002F07\u002FManufacturing.png",[72,559,560],{"id":560},"灌装与密封",[14,562,563],{},"灌装与密封步骤是将药品放入其一级包装，并确保其牢固密封。",[355,565,566,572,578],{},[358,567,568,571],{},[76,569,570],{},"无菌环境","：对于需要无菌的药物，此步骤在洁净室环境中进行，以防止污染。",[358,573,574,577],{},[76,575,576],{},"自动灌装","：利用自动化机械将正确的药物剂量精确灌入包装单元，确保精度和一致性。",[358,579,580,583],{},[76,581,582],{},"密封","：确保一级包装妥善密封，以保护药物免受外部因素影响。这可能涉及热封、超声波密封或粘合剂涂覆等技术。",[72,585,586],{"id":586},"标注",[14,588,589],{},"准确标注对于合规和患者安全至关重要。",[355,591,592,598,604],{},[358,593,594,597],{},[76,595,596],{},"标签制作","：设计包含所有强制信息的标签，如药物名称、用药说明、活性成分、批号、有效期和生产商详情。",[358,599,600,603],{},[76,601,602],{},"印刷与粘贴","：使用高质量的油墨和材料印刷标签，以确保耐用性和可读性，随后通过自动或手动流程将其粘贴到一级和二级包装上。",[358,605,606,609],{},[76,607,608],{},"核验","：进行全面检查，确保所有标签准确无误且粘贴正确。这一步骤对于满足监管要求和确保安全至关重要。",[72,611,612],{"id":612},"二级与三级包装",[14,614,615],{},"一级包装完成灌装、密封和标注后，即被放入二级和三级包装中以供分销。",[355,617,618,624,630],{},[358,619,620,623],{},[76,621,622],{},"装盒","：将一级包装单元放入纸箱或盒子等二级包装中。此步骤还可能包括加入为患者和医疗专业人员提供额外信息的包装说明书。",[358,625,626,629],{},[76,627,628],{},"集合包装","：将二级包装归组为更大的单元以便运输，可能涉及将纸箱放入更大的箱子或托盘上。",[358,631,632,635],{},[76,633,634],{},"安全特征","：在二级和三级包装上加入防拆封特征和序列化代码，以增强安全性和可追溯性。",[72,637,638],{"id":638},"质量保证",[14,640,641],{},"质量保证（QA）是贯穿各包装阶段的持续过程。",[355,643,644,650,656],{},[358,645,646,649],{},[76,647,648],{},"过程中检查","：在包装过程的每个阶段定期检查和测试，及时发现并纠正任何问题。",[358,651,652,655],{},[76,653,654],{},"最终检验","：对成品进行全面检验，确保其符合所有质量标准和监管要求。",[358,657,658,661],{},[76,659,660],{},"文档记录","：详细记录包装过程，包括所用材料、测试结果和 QA 检查。这些文档对于合规和可追溯性至关重要。",[72,663,664],{"id":664},"分销与物流",[14,666,667],{},"最后一步是为分销准备包装好的产品。",[355,669,670,676,682],{},[358,671,672,675],{},[76,673,674],{},"储存","：确保包装好的产品在能够维持完整性和稳定性的条件下储存，如受控的温度和湿度。",[358,677,678,681],{},[76,679,680],{},"运输","：协调将包装好的产品运往配送中心、药店和医疗机构的物流。这包括确保运输条件符合监管要求并保护产品免受损坏。",[358,683,684,687],{},[76,685,686],{},"供应链管理","：实施系统以追踪和管理包装产品在整个供应链中的流动，确保及时高效地交付。",[42,689,690],{},[45,691,692,694],{},[48,693],{},[51,695],{"alt":664,"height":248,"src":696,"width":56},"\u002Fimages\u002F2024\u002F07\u002FDistribution-and-logistics.jpg",[58,698,699],{"id":699},"结语",[14,701,702],{},"医药包装是制药行业的重要组成部分，涵盖一系列用于保护和告知的材料与流程。",[14,704,705],{},"遵循全球标准和本地法规（如印度的 QR 码要求），可确保制药公司产品的安全性和有效性。",[14,707,708],{},"带有数字链接的 GS1 2D 条码等先进解决方案显著增强了包装，改善了可追溯性、防伪和安全性。医药包装市场持续发展，不断整合创新技术，以满足全球市场日益增长的需求。",{"title":710,"searchDepth":711,"depth":711,"links":712},"",3,[713,715,722,727,734,739,753,754,759,762,772],{"id":60,"depth":714,"text":61},2,{"id":70,"depth":714,"text":70,"children":716},[717,718,719,720,721],{"id":74,"depth":711,"text":74},{"id":83,"depth":711,"text":83},{"id":91,"depth":711,"text":91},{"id":99,"depth":711,"text":99},{"id":107,"depth":711,"text":107},{"id":124,"depth":714,"text":124,"children":723},[724,725,726],{"id":130,"depth":711,"text":130},{"id":138,"depth":711,"text":138},{"id":146,"depth":711,"text":146},{"id":163,"depth":714,"text":163,"children":728},[729,731,732,733],{"id":170,"depth":730,"text":170},4,{"id":178,"depth":730,"text":178},{"id":186,"depth":730,"text":186},{"id":194,"depth":730,"text":194},{"id":211,"depth":714,"text":211,"children":735},[736,737,738],{"id":217,"depth":711,"text":217},{"id":225,"depth":711,"text":228},{"id":234,"depth":711,"text":234},{"id":252,"depth":714,"text":252,"children":740},[741],{"id":258,"depth":711,"text":258,"children":742},[743,744,745,746,747,748,749,750,751,752],{"id":261,"depth":730,"text":261},{"id":269,"depth":730,"text":269},{"id":277,"depth":730,"text":277},{"id":285,"depth":730,"text":285},{"id":293,"depth":730,"text":293},{"id":310,"depth":730,"text":310},{"id":318,"depth":730,"text":318},{"id":326,"depth":730,"text":326},{"id":334,"depth":730,"text":334},{"id":342,"depth":730,"text":342},{"id":350,"depth":714,"text":350},{"id":387,"depth":714,"text":387,"children":755},[756,757,758],{"id":393,"depth":711,"text":393},{"id":401,"depth":711,"text":401},{"id":409,"depth":711,"text":409},{"id":420,"depth":714,"text":421,"children":760},[761],{"id":427,"depth":711,"text":430},{"id":461,"depth":714,"text":461,"children":763},[764,765,766,767,768,769,770,771],{"id":467,"depth":711,"text":467},{"id":493,"depth":711,"text":493},{"id":525,"depth":711,"text":525},{"id":560,"depth":711,"text":560},{"id":586,"depth":711,"text":586},{"id":612,"depth":711,"text":612},{"id":638,"depth":711,"text":638},{"id":664,"depth":711,"text":664},{"id":699,"depth":714,"text":699},"Digital Link 的 QR 码如何助力医药包装：将产品安全、有效性与合规性融于一码之中。","md","医药包装：全球标准与本地要求指南","article",{},true,"\u002Fimages\u002F2024\u002F07\u002F9-packaging-for-pharmaceutics.png","\u002Fzh-hans\u002Fguides\u002Fpharmaceutical-packaging","2024-07-24T18:45:12+02:00",{"title":5,"description":773},"\u002Fzh-hans\u002Fguides\u002Fpharmaceutical-packaging\u002F","zh-hans\u002Fguides\u002Fpharmaceutical-packaging","2024-07-25T14:46:44+02:00","l9DM7GNsYClpwc1reBsH0YkWERt9cT2RcZ5mH04pz4k",[788,794,800],{"path":789,"sourcePath":790,"title":791,"heading":6,"ogImage":792,"publishedAt":793},"\u002Fzh-hans\u002Fguides\u002Feu-detergents-regulation-digital-product-passport","\u002Fzh-hans\u002Fguides\u002Feu-detergents-regulation-digital-product-passport\u002F","欧盟洗涤剂法规数字产品护照","\u002Fimages\u002F2026\u002F03\u002FEU-Detergents-Regulation-Digital-Product-Passport.webp","2026-03-30T18:45:23+02:00",{"path":795,"sourcePath":796,"title":797,"heading":6,"ogImage":798,"publishedAt":799},"\u002Fzh-hans\u002Fguides\u002Feu-construction-products-regulation","\u002Fzh-hans\u002Fguides\u002Feu-construction-products-regulation\u002F","欧盟建筑产品法规 2024\u002F3110","\u002Fimages\u002F2026\u002F02\u002FEU-Construction-Products-Regulation-20243110-and-the-Digital-Product-Passport.webp","2026-02-16T17:33:30+01:00",{"path":801,"sourcePath":802,"title":803,"heading":804,"ogImage":805,"publishedAt":806},"\u002Fzh-hans\u002Fguides\u002Fproduct-page","\u002Fzh-hans\u002Fguides\u002Fproduct-page\u002F","用智能产品页优化产品页面","如何用 Digital Link 打造高转化的产品页面","\u002Fimages\u002F2025\u002F10\u002FProduct-page.png","2025-10-29T18:15:32+01:00",1785948095376]