Conferences on May 09, 2012

Held over 3 days, ARBS 2012 will showcase all the latest technology for the HVAC & R and building services industry. ARBS is the only trade event of its kind in Australia that delivers solutions and innovations for residential, commercial and industrial air conditioning and refrigeration. Attend one of our informative seminars promoting best practice or become a high achiever by nominating for the ARBS awards program in a range of categories. If you are involved in the HVAC & R and building services industry, you cannot afford to miss ARBS 2012.

The international laundry and dry cleaning industry will be meeting in Frankfurt am Main from 05 to 09 May 2012, the world market for modern textile care. This important event gives investors and decision-makers from all over the world the opportunity to find out about the latest trends and innovations.

ARBS 2012 is Australia’s trade exhibition for the air conditioning, refrigeration and building services industries. Showcasing the very latest innovations and technologies ARBS connects local, national, and international exhibitors with major buyers, specifiers, design and consulting engineers and technicians. This major HVAC & R and building services event is held over 3 days and features the trade exhibition, an informative seminar program and the national awards gala event.

SNEC (2012) PV POWER CONFERENCE will focus on the KEY TOPIC about how to make the photo voltaic industry obtain a rapid, steady and sustainable growth through enhancing international exchanges and cooperation, accelerating the technology upgrading, guaranteeing the high quality of products, and promoting the application market expansion, especially under the trend of developing a low-carbon economy as well as building a low-carbon society.

Desert Green is the MENA Regions Premier Sustainable Agriculture Conference and Exhibition

This FDA software validation Webinar/training will discuss how to self audit and ensure validation and software quality processes that will pass FDA inspection. Why Should You Attend: FDA Commissioner Margaret Hamburg recently announced several new enforcement initiatives. They are certain to impact your regulatory risk profile. How will you prepare for software quality, software validation and 21 CFR part 11 planning? Pharma, Biotech and Medical Device manufacturers are self-regulated with FDA oversight. By the time FDA come to your door, it may be too late to bring order to chaos. Companies have the responsibility to self audit to ensure compliance to GMP regulations. FDA inspectors are trained to know what to look for - you should too! Internal audits can be used for process ...

This webinar will explain what protected concerted activity means, including online activities (for example, Facebook wall posts) and will cover areas such as your social media policy and your policy on revealing wage information. Union membership is at an all-time low. As a result many companies think the National Labor Relations Act is unimportant to most companies. Unfortunately nothing could be further from the truth. The current National Labor Relations Board is very active in dealing with situations that deal with union and non-union company actions. Much of their activity centers on what is called “protected concerted activity.” These are rights afforded to employees by the National Labor Relations Act regardless of whether an employee is covered by a union contract or not. This ...

The conference aims at bringing key industry figures together to debate and discuss various topics and advancements in the investment and project finance sector. The event will illustrate how to bring investment to Africa and highlight on the key industries that investors can take advantage of. The conference will also focus on the projects that are booming in Africa creating room for both local and foreign investors to partner with governments.

Explore new career opportunities this May! Bring many resumes and interview for the many opportunities available in cyber security, information technology, engineering, aerospace, telecom, project management, intelligence, operations, homeland security, research & more at TECHEXPO Top Secret's May hiring events! Wednesday, May 9th • 10am - 3pm BWI Marriott 1743 West Nursery Road Baltimore, MD 21090 Directions Only: 410.859.8300 Pre-Register: www.TECHEXPOUSA.com Admission: Any level of Active Security Clearance issued by the US Federal Government or Military is REQUIRED to attend (or clearance last used within past 24 months.)

The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when one change is major enough to impact safety / effectiveness, or when a series of lesser changes finally reach the "tipping point". This is a major headache. How can companies make that determination? How can they trigger such an analysis over the major change or the series of smaller changes. What approaches are required for product changes; for process changes. How is the process risk-based? How to maximize the process against scarce resources. What are the different considerations for CE-marked product? Areas Covered in the Session: U.S. FDA device clearance / approval FDA's and EU's emphasis Product ...