Events
BSI Management Systems delivers web-based seminars and Regional Forums addressing key topics that affect your business including legislation, risk, and key drivers for implementation.
Wednesday February 10, 2010
1:00PM to 2:00PM EST
Many organizations use ISO/IEC 27002 (previously ISO/IEC 17799) to implement IT security controls, but is this really the right place to start? Does it mean that organizations are paying too much for Information Security? This webinar will examine what a management system is and why it’s important to have one in place. It will also provide an overview of the ISO/IEC 27001 management system and will look at different ways an organization can begin to implement ISO/IEC 27001.
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Wednesday, February 10, 2010
3:00 PM to 4:00 PM EST
As we begin the new decade, manufacturers, distributors and others involved in the importation of medical devices, pharmaceuticals and other healthcare items are experiencing an unprecedented increase in new Government initiatives, and, in turn, new compliance responsibilities. The FDA’s $166 Million Safer Medical Products and PREDICT Initiatives, CBP’s new Commercial Targeting Analysis Center (CTAC), and the expansion of C-TPAT and other global Supply Chain Security Programs are affecting a real and lasting change for the healthcare supply chain.
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Wednesday February 17, 2010
1:00PM to 2:00PM EST
Throughout 2010, BSI will be running a series of webinars dedicated to ISO/IEC 20000. Each session will concentrate on one part of the standard. The first of the IT Service Management webinar series will provide a general overview of ISO/IEC 20000, its purpose and suitability for organizations. It will also look at the overall benefits of the standard as well as the organizational problems it addresses. Finally, the webinar will look at how ISO/IEC 20000 relates to ITIL version 3.
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BSI Passport to Europe Series
Thursday February 18, 2010
1:00pm - 2:00pm EST
ISO 13485 is an internationally recognized standard for medical device Quality Management System (QMS). Certification is frequently viewed as an initial step in the path of achieving conformity to CE marking regulations, which then allows manufacturers to sell their devices in the 27 countries of the European Union.
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Monday February 22, 2010
1:00pm - 2:00pm EST
Section 4 of ISO 9001 describes the general requirements for an organizations quality management system. It provides the documentation requirements including the requirements for the quality manual and the control of documentation within the organization, including records. The standard is based on the P-D-C-A; Plan – Do – Check – Act cycle adopted by all the ISO quality and environmental standards. The scope of the Quality Management System – Requirements are defined in section 1.1 of the standard and relate directly to each of the elements included within the Standard’s requirements. This webinar cover the basic requirements for documentation along with the concept of Plan, Do, Check, Act.
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Wednesday February 24, 2009
1:00pm – 3:00pm EST
General overview of the AS program and scheme status including current timelines for final release of all standard documentation as well as AQMS implementation requirements for companies certified to AS 9100. Detailed overview of the revised AS standards and changes and their impact on clients registered to AS9100 and the overall registration process.
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Thursday February 25, 2010
1:00pm – 2:00pm EST
Would you spend an hour to learn how you can seize control of your data, increase visibility into your operations, and automate your reporting?
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Multiple Events and Locations
1:30pm – 4:00pm
Join us for our next BSI Regional Business Forum and gain an understanding of how leading organizations around the world are leveraging their use of BSI’s Entropy Technology Solution to drive quality, performance, and sustainability while mitigating organizational risk.
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Multiple Events and Locations
9:00am – 11:30am
Is Your Supply Chain Secure? Manage Risk and Compliance
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Wednesday March 17, 2009
1:00pm – 2:00pm EST
An Environmental Management System (EMS) has become increasingly important to every industry and for organizations of every size. But, where to start? With ISO 14001, the internationally accepted standard for EMS, your organization can develop and sustain the delicate balance between maintaining profitability and reducing the impact your organization has on the environment. Learn how to define, measure, and monitor your organization’s effect on the ecosystem.
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BSI Passport to Europe Series
Thursday March 18, 2010
1:00pm - 2:00pm EST
Are you aware of the impact Clinical Evaluation has on placing your Medical Device in the European Union? This exciting market is made up of 27 countries and if you want to sell your product in Europe, obtaining a CE Mark is mandatory. This requires a Device manufacturer to comply with the European Medical Device Directive (MDD) regulations in which Clinical Evaluation is a key requirement.
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Tuesday March 30, 2010
1:00pm - 2:00pm EST
The second webinar of the series will provide a more in-depth definition of a Management System, why it's important and how it works with ISO/IEC 20000. The webinar will cover:
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BSI Passport to Europe Series
Thursday April 8, 2010
1:00pm - 2:00pm EST
Risk Management continues to receive increased attention and can be challenging for many medical device manufactures. It is an important part of the integrated regulatory process to achieve CE marking, which is a legal requirement to sell a device into the 27 countries of the European Union. Another vital part is an effective Quality Management System (QMS). The majority of manufacturers base their QMS on the ISO 13485:2003 standard which in turn requires the organization to establish documented requirements for risk management.
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