Thursday, March 13, 2014

ISO 18091

 ISO 18091 is the first ISO standard for the governmental sector that gives guidelines for the implementation of ISO 9001 in local government.

http://www.iso.org/iso/home/news_index/news_archive/news.htm?refid=Ref1825

綠色辦公室如何提升企業品牌形象?- From BSI HK




Description: Description: Description: BSI_Brand



綠色辦公室如何提升企業品牌形象?


企業為了提升品牌形象,固然重視推出產品和服務質素,近年更講求公眾形象,不少更會在環保方面下功夫,包括參與綠色辦公室計劃、環保比賽、取得相關認證及獎項等等,但他們是如何踏出第一步?又如何克服當中的困難呢?

講座內容
1. 如何成為一個值得信賴的品牌及提升品牌價值

演講嘉賓:
英國標準協會(BSI) 銷售及市場總監 謝健雄先生
2. 聯合國千禧年發展目標 - 綠色辦公室獎勵計劃  企業案例分享

演講嘉賓:
世界綠色組織 (WGO)項目發展經理 陳恩光先生
3. 綠色辦公室:如何在辦公室推動環保

    演講嘉賓:          香港資源控股有限公司
                                 投資關係部主管 余海恩小姐


詳情
日期:
2014317日(星期一)
Description: http://thewgo.org/eflyer/GOALS-CSR3/images/map.jpg
時間:
下午3時至5
(下午2:30開始登記)
地點:
香港港島東英皇道979號太古坊康橋大廈23 (鰂魚涌港鐵站A出口)
費用:
免費 (名額有限)
報名及
查詢:
莊倩衡小姐
電話:3149 3331電郵:jamie.chong@bsigroup.com



Friday, March 7, 2014

研讨会 - 德国莱茵TUV是您可信赖的测试伙伴

德国莱茵TUV是您可信赖的测试伙伴



TUV Rheinland
New Test Mark
Hotline 全国服务热线 4008831300 +852 21921022
TUV莱茵2月份研讨会
1
德国莱茵TUV研讨会 TUV Rheinland Seminar

纺织品,玩具与化学测试3月份研讨会(免费)
Textile, Toy and Hazardous Chemical Testing seminar in March (Free)

为协助客户将安全和高品质的消费产品销往世界各地,TUV莱茵纺织品、玩具及化学业务线将在3月举办下列免费研讨会,如有兴趣,敬请点击“我要报名”在线申请。
To help you supplying safe and high quality consumer products around the world, TUV Rheinland invites you to attend the below seminars in March.
1

研讨会安排:
研讨会主题
Subject
时间
Time
 点 
Location
内容
Contents
服装与鞋类产品中的有害化学物质研讨会
Restricted chemicals in fashion apparel and footwear products
我要报名
Online Registration
2014-03-14
14:00-16:00
本次研讨会的目的是为大家分享有关纺织品和鞋类产品中的有害化学物质,如:偶氮染料,致敏致癌染料,镉,富马酸二甲酯,甲醛,重金属,六价铬,镍,铅,五氯酚,邻苯二甲酸盐等,受限制的化学物质。
English Version
玩具GS认证以及蹦床测试介绍Intro. of GS Mark requirements for toy; TOYPROOF Mark and trampoline testing
 
我要报名
Online Registration
2014-03-21
14:00-16:00
玩具GS标志是一个有效的市场行销推广工具,用以增强客户对玩具产品的信心和增加他们的购买欲。GS标志采纳了德国国家制定的严谨标准作评核,因此它深受世界各地买家及消费者的认同及肯定。本次会议介绍:
1. GS认证程序
2. 法规和额外认证要求
3. 文件准背
4. 蹦床的当前标准和测试介绍

English Version
欧盟REACHRoHS
法规详解
EU REACH and RoHS regulations update
 
我要报名
Online Registration
2014-03-28
14:00-16:00
欧盟针对已有的REACH法规和RoHS指令公布了新修正案。更新内容包括一些化学物质的限制使用,REACH法规附件的更新等,如:欧盟REACH法规中提到的高关注物质清单(SVHCs)和其他受限制化学品(增塑剂,多环芳烃,镉和其他物质),RoHS以及协调标准 EN 505812012等条例。
English Version
鞋履品质检测研讨会
General footwear testing seminar
我要报名
Online Registration
2014-03-14
14:00-16:00
本次研讨会主要是为参会者详细介绍鞋履产品在欧美市场的有关测试方法及部份要求。包括整鞋和鞋材一般需要的测试项目及其相关测试的介绍,让参会者对鞋履品质有一个更专业的认识和判断,明确产品最终进入市场所必须具有的相关标示等等。
English Version
欧盟REACHRoHS法规详解EU REACH and RoHS regulations update
我要报名
Online Registration
2014-03-26
14:00-16:00
此次研讨会的目的是介绍欧盟市场针对消费品中常见化学有害物质相关资讯。包括REACH法规更新,限制的151项高度关注物质,授权物质清单,物质注册等;RoHS2.0的标签要求、技术文档等最新修订。此次研讨会提供的详细内容,均以配合您的业务需求。本次研讨会内容充实、有针对性,相信对企业具一定的参考价值。
English Version
欧美针对仿真饰品饰品的法律法规
Laws & Regulations on imitation Jewelry in EU & US
我要报名
Online Registration
2014-03-20
14:00-16:00
此次研讨会主要介绍关于儿童珠宝饰品及成人仿真饰品的法律法规,也会展示REACH法规对仿真饰品的要求,主要关注:
1. 加拿大消费品安全法案及儿童首饰条例下的安全要求
2. 美国
ASTM儿童珠宝新标准ASTMF2923-11
3. 儿童珠宝与成人珠宝的测试要求差别
4. REACH法规对于仿真首饰的要求及内容

English Version
欧盟REACHRoHS法规详解EU REACH and RoHS regulations update
我要报名
Online Registration
2014-03-19
14:00-16:00
此次研讨会的目的是介绍欧盟市场针对消费品中常见化学有害物质相关资讯。包括REACH法规更新,限制的151项高度关注物质,授权物质清单,物质注册等;RoHS2.0的标签要求、技术文档等最新修订。此次研讨会提供的详细内容,均以配合您的业务需求。本次研讨会内容充实、有针对性,相信对企业具一定的参考价值。
English Version
欧盟REACHRoHS 
法规详解
EU REACH and RoHS regulations updates
我要报名
Online Registration
2014-03-24
13:30-16:00
此次研讨会的目的是提供最新的行业信息和更新,欧盟REACH规更新,RoHS中限制的化学品。内容包括REACH法规授权的候选名单,RoHS的标签要求等。而且,产品中常见化学物质的有关咨询亦会提及。此次研讨会提供的详细内容,均配合您的业务需求。
English Version
德国、其它欧洲国家玩具的物理及化学要求更新
Updates on the physical and chemical requirements of toys for Germany, other EU countries.
我要报名
Online Registration
2014-03-27
14:30-17:00
此次研讨会的主要议题包括在德国市场及其它欧洲国家市场玩具的物理及化学要求简洁,了解各国的玩具安全法规标准,可以帮助保持产品的安全质量。我们欢迎所有的产品制造商,采购商和出口商来参加这次研讨会。座位有限,请立即报名。
English Version

德国莱茵TUV是您可信赖的测试伙伴。
本次研讨会特别为有关企业量身定制!名额有限,请速报名!

德国莱茵
TUV日前正式开通Webex 线上研讨会平台
https://tuvrheinland.webex.com.cn我们会陆续推出更多热门课程,欢迎各位收藏平台地址。我们更将部分研讨会录制成影片,欢迎点击收看。如有任何疑问,请与我们联系:
seminar@chn.tuv.com
TUV Rheinland is your reliable partner.
This seminar is specially made to fit your business, seats limited, register ASAP.

TUV Rheinland proudly introduce you Webex Seminar platform:
https://tuvrheinland.webex.com.cn  We will be bringing you more online seminars soon. Some of the seminars will be recorded, please bookmark the link. Any enquiries please contact us: seminar@chn.tuv.com


联系人

叶小姐 Ms.Suki Yip
电 话
邮 箱
TUV Rheinland

Wednesday, February 5, 2014

A Lesson in Risk-Based Supplier Quality Management [Executive Q&A]


A Lesson in Risk-Based Supplier Quality Management [Executive Q&A]

  
  
Share26  
brian rhatiganManaging supplier quality in the pharmaceutical manufacturing industry is a challenge for most organizations, even the ones that do it well. In a space where precision is key, slight variations in processes, equipment used, or materials sourced by suppliers can quickly result in rejects and dissolved relationships. These variations really highlight the need for a seamless supplier quality management system, which is what market leaders are continuously working toward.  
To dive deeper into this topic, last week we had the opportunity to speak with Brian Rhatigan, Director of Supplier Quality Assurance at Catalent Pharma Solutions, a global leader in development solutions and advanced delivery technologies for drug, biologic, and consumer health products. Working with 49 of the world’s top 50 pharmaceutical companies, Catalent has a global network of suppliers it relies on. Rhatigan’s supplier quality team has been tasked with optimizing the quality and compliance aspects of those relationships.
A central theme from our conversation with Rhatigan surrounded taking a risk-based approach to supplier quality management. He detailed the journey his team has been on to transform Catalent’s supplier relationships into a source of competitive advantage. A number of the transformations have been technological and process-oriented in nature. Below is an excerpt from our interview (full interview here).

LNS: Since you took over as Director of Corporate Supplier Quality in early 2013, what have been your main areas of focus?

BR: In terms of our ability to manage supplier quality, we’re always evolving and striving to improve. Since I took on this role, my team and I have been working on a number of initiatives. Mainly, we have been putting our efforts intostandardizing and centralizing the audit management process, and then into taking that a step further by adding an element of supplier risk management. Better utilizing the technology available to us has been a focus as well.

LNS: Standardizing and centralizing processes is instrumental to identifying areas for improvement and realizing real gains across the enterprise. How have you gone about doing that with your supplier audit process?

BR: With acquisitions and a number of distributed facilities, we’ve had redundancies in the audit process. Many sites had their own processes, and there wasn’t a corporate standard. Our audits were carried out via questionnaires or by one of our auditors physically going to the site. With this approach, we met the regulatory requirements, but it wasn’t necessarily the most efficient or cost-effective method.
In the past six months we’ve developed a quality action plan for the entire enterprise. The first step has been enhancing the building blocks–policies and standards–those things that will drive actual activities such as risk assessment, audit standards, monitoring supplier quality, and so on. We’ve been rolling that out, training personnel and building out processes and tools people need to accomplish the task at hand.

LNS: Risk management and supplier quality go hand in hand. How are you using risk management to improve your supplier quality audits?

BR: In the past, we’ve used a matrix model, where we knew the type of supplier and determined the frequency of audits required based on that. Recently, we’ve been transitioning to a risk-based model, putting more focus on evaluating the performance of suppliers along with evaluating the type of material or service provided and determining how much attention each evaluation required. Switching to evaluating suppliers based on performance requires considerable training as well as process standardization and has its own set of challenges, but we have a plan and are working our way through it.
After standardizing and centralizing the process, the goal is to minimize the number of redundant audits. And then taking a risk-based approach, we’ll actually know which suppliers are more risk-prone and therefore require more attention versus auditing suppliers arbitrarily or because a certain amount of time has passed. Some need to be audited in 3 years, some in 5 years. Our new approach enables us to more strategically use our resources.

LNS: Having been working on this project for the past 6 months, what kind of benefits have you experienced since it started?

BR: One of the most notable advantages has been connecting what were traditionally individual silos, now putting all of that information in a central location. In that respect, we’ve been able to reduce workload significantly, and it’s surfaced in financial and efficiency improvements. We’ve been able to cut down the number of redundant audits, reducing our total number of audits by 15-25%, which translates to several hundred thousand dollars in savings. Also we are focused on the suppliers who might need more oversight and therefore our efforts are where they matter most. The advantages will only increase as our risk-based model becomes more prevalent. The increased transparency has resulted in other benefits as well.

LNS: What has been the role of technology in this project and how do you plan to leverage it more in the future?

BR: We’ve been using an industry recognized quality management software solution to document and track our information. While a lot of our supplier quality processes have been manual in nature, we’re making changes to our workflows and working to automate them.
Long-term we plan to build a supplier dashboard with real-time information being pumped in so we easily see internal and external supplier metrics and Key Performance Indicators, and start judging their performance the way we judge the performance of ourselves. Our goal is to develop a world-class supplier quality system and we’re moving toward that.
In the past several weeks, we’ve interviewed a variety of quality directors, VPs, and CEOs. If you want to share your experiences in quality and be highlighted on the LNS Research Operational Excellence Blog, email me atmike.roberts@lnsresearch.com or tweet to me @mp_roberts.
To read the full interview and an overview of LNS Research's systematic approach to supplier risk management, click here or follow the button below.
SQM report