Conferences on August 21, 2012

Overview : Every manager encounters employees who cross the line into unacceptable behavior. Maybe they tell off-color jokes. Spread gossip. Act like slobs. Practice poor personal hygiene. Ridicule core organizational values. Or violate company rules and policies. Lots of managers don't have the toolkit to confront dysfunctional employees so they practice avoidance, which erodes morale and - worst of all - destroys their own credibility. Great managers recognize that putting a stop to unacceptable behavior requires a complex mix of communication skills, persuasion, intuition, toughness and credibility. They know how to probe for the reasons behind the behavior, anticipate reactions, manage expectations, seek alignment, set boundaries and hold people accountable. When bosses learn how to ...

US federal organizations rely on Accenture Federal Services for a broad range of consulting, technology and outsourcing solutions to help them do even more with even less and deliver maximum outcomes in minimum time. In fact, every cabinet level agency in the United States—and 20 of the country’s largest federal government agencies—has worked with Accenture to achieve outcomes and move toward high performance. Accenture Federal Services is hiring into: - BWI/Fort Meade, MD - Arlington/Reston/Herndon, VA - San Antonio, TX Join us at our open house: Tuesday, August 21st • 10am – 3pm BWI Marriott 1743 West Nursery Road Baltimore, MD 21090 All candidates must have a minimum TS/SCI Security Clearance to Attend. Register to Join Us http://www.AccentureExpo.com ...

This 90-minute session on risk-based verification and validation planning will discuss "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's quality management system. Why Should You Attend: FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies. And now the FDA is taking an even tougher stance. One major failing is lack of sufficient or targeted risk-based V&V planning. Why do companies need a Master Validation Plan? What are the must have elements from ISO 14971 and ICH Q9 for hazard analysis and product risk management? How can these be integrated into a company's quality management ...

This 120-minute webinar will help medical device manufacturers to understand what you need to do to ensure that your process, the methods, and the procedures that you have established to implement the requirements for design controls are in perfect order. Why Should You Attend: In the global economy and supplier partnership, it is critical that every product development process for product, service or logistics, is well designed - that the design inputs are well defined, design outputs are documented and auditable as well as design transfers are successful. There are millions of dollars spent on design transfers that are not effective - and instead of creating a benefit and remove liability, they instead increase the liability and risk.

This 90-minute webinar will show how to evaluate disinfectants against the types of microorganisms recovered from the cleanroom environment. You will learn how to design and execute an effective disinfectant qualification study that provides a scientific rationale for developing an effective disinfection/cleaning program. Why Should You Attend: Proper selection and use of disinfectants are critical to microbial contamination control in aseptic processing environments. To evaluate disinfectants a good understanding of methods available to perform disinfectant qualification studies is important. This 90-minute webinar provides the exact guidance required for selecting disinfectants, planning and costing a disinfectant qualification study, important elements of the study protocol, ...

OMICS Group invites all the participants across the globe to attend the International Conference and Exhibition on Nephrology and Therapeutics 20-22 August 2012, Hilton Chicago/Northbrook Chicago, USA.

To Collaborate Scientific Professionals around the World Dates of the Conference 21–22 August 2012 Venue of the Conference Chicago, USA Theme A Frame Work For Understanding the Complex Interactions Among Key Elements of Earth Systems Sponsors Click here for Sponsorship Opportunities Speaker Opportunity Day 1: Day 2: Available Available Poster Opportunity Available

The International Conference & Exhibition on Addiction Research & Therapy will schedule and coordinate all meetings with our Editorial Board Members and other experts in the Addiction Research and Therapy field across the World. The scientific program paves a way to gather visionaries through the research talks and presentations and put forward many thought provoking strategies in Addiction Research & Therapy Addiction Therapy -2012 highlights the following topics: • New Therapeutic aspects for Addiction • Current Research on Addiction • Drug Addiction and Neurotoxicology • Addiction Case Reports • Various Addictives and Addictions • Alcoholism and Therapy • Cocaine Addiction and therapy • Treatment and Rehabilitation using Various Therapies • Drug Addiction ...

OMICS Group invites all the participants across the globe to attend the 2nd World Congress on Vaccines & Vaccination during 20-22 August 2012 at Chicago, USA. Vaccines-2012 is a remarkable event which brings together a unique and International mix of large and medium biotechnological companies / industries, leading universities and research institutions making the conference a perfect platform to share experience, foster collaborations across industry and academia, and evaluate emerging technologies across the globe.

Who would exhibit? •Air conditioner equipment & corollary equipment •Refrigeration & freeze, refrigerated storage technology and equipment •Ventilation & circulating water equipment: •Electric & automatic control equipment