Events
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The Online Seminar shows the Possibilities of the use of Desktop-Sharing Software. The Online-Seminar is free of charge an will contain the following topic. How to Setup the Software. The Webinar will held on request, the duration is approx. 30 Minutes Further Information to the Online-Seminar Learn more: www.practicepaysolutions.com/mastery Join us for a free series of one-hour webinars with the a team of industry experts! We're presenting the less-covered, critical issues for small business owners, so you can reduce the time you spend on set-up and administration-- and focus on what really matters. Can't attend live? We'll send you the call recordings so you can access valuable information and share the event with your community! April 2nd: The Joy of Productivity with George Kao April 16th: How to Create Profitable Referral Partnerships with Robert Notter April 24th: Say Bye-Bye to Your Boring Bio with Nancy Juetten May 15th: From Contacts to Contracts with Caterina Rando May 22nd: Red Fire Profitability with Liz Goodgold June 5th: Developing Contracts & Service Agreements with Tasha Cooper Coleman June 19th: Outsourcing Secrets with Travis Greenlee July 10th: Your Money Relationship = Your Business Success with Helen Kim July 24th: How to Play a Bigger Marketing Game with Fabienne Fredrickson Allan Gonsher and Kids Inc are pleased to a offer a series of Play Therapy Webinars. If your work with children, or want to work with children, these are workshops that you can not afford to miss. Each webinar workshop offers one hour of continuing education credit. Start: 07/12/2012 7:10 am
Overview: No or inadequate training of employees is one of most frequently cited deviations in FDA inspectional observations and warning letters. Trainings are either not planned, not conducted, not evaluated or not documented as expected by inspectors. On the other hand it has been is estimated that about 5% of employee's time is spent for training. So there seems to be lack of understanding on what the regulations are, their interpretations and expectations of inspectors. This webinar will give a good understanding of FDA requirements for training and provide recommendations for implementation. Reference material for easy implementation: Who Will Benefit: Start: 07/12/2012 10:00 am
End: 07/12/2012 11:30 am
This 90-minute webinar will focus on the critical steps in starting up a new cleanroom operation and releasing it for manufacturing. It includes a case study-based approach to dealing with excursion events and establishing control of the cleanroom after a worst case event. Why Should You Attend: This webinar will focus on starting up a new cleanroom operation covering from utilities to environmental monitoring. Routine cleaning and disinfection will also be addressed. Addressing contamination and bringing up the cleanroom after a worst case even will be discussed. Cases studies on bringing up the site after a worst case event will be discussed in detail. Excursion investigations will also be discussed and troubleshooting parameters and suggestions will be discussed. Areas Covered in the Seminar: - The critical steps needed to release the room for manufacturing will be discussed. Start: 07/12/2012 10:00 am
End: 07/12/2012 11:30 am
This Clinical trial auditing training will provide an understanding of how to conduct compliant and successful clinical trials by defining FDA clinical trial audit procedures, audit program, audit planning and audit preparation. Why Should You Attend: The field of GCP has rapidly evolved over the last few years and the requirements are getting tougher. Many companies find themselves unprepared for a clinical trial audit, either at a clinical site or their headquarters. This course will help you to prepare early and help to prevent surprises when being audited. Learn to identify risks and handle them to build a more compliant and successful trial. This training will also share the ”audit experience”, by sharing what auditors look for and how to prepare for the visit. Define expectations, train your staff and hold them accountable and the inspection will be easy to manage. We will describe proactive measures you can take to assure that all systems are in place, operating well and operating in compliance. Areas Covered in the Seminar:
Start: 07/12/2012 11:00 am
This webinar explores Social Anxiety Disorder, or Social Phobia, and its relationship to other disorders via assessment, treatment, and prevention, as well as how to help improve the personal, financial, and social life of clients. Full Description: treatable, condition. Based on current research, this course provides the most up-to-date information on diagnosis, assessment, and treatment of Social Anxiety Disorder and its relationship to other anxiety disorders. Attendees will leave the webinar with a renewed awareness of the personal, financial, and social costs of this significant public health problem. Course Includes: What You Will Learn: Your Presenter: Joseph Hospital, Dr. Morris currently teaches psychology courses at Indiana University in Kokomo, Indiana. Dr. Morris received her doctorate in clinical psychology from Indiana University in Bloomington, Indiana. She also completed a postdoctoral appointment at the University of Pittsburgh in Behavioral Weight Control. While in Pittsburgh, she developed a special interest in the treatment of depression and anxiety disorders using a Cognitive-Behavioral approach. Disclaimer: attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event. Technical requirements: time, you can setup prior to the meeting by following this link: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Practitioners, Case Managers, Alcoholism and Drug Abuse Counselors/Addiction Professionals, Clergy Start: 07/12/2012 12:00 pm
End: 07/12/2012 12:40 pm
Space is limited Complimentary Lunch & Learn Webinar: Microsoft Office 2010 Tips & Tricks This session is ideal for users who have recently upgraded to Microsoft Office 2010, and who want to get up to speed quickly and learn valuable tips to save time, create user-friendly documents, present information in a compelling way, and analyze data with ease. We will start with the overall Office 2010 navigation and options, and then move to PowerPoint to demonstrate themes and layouts, then to Excel to see some of the powerful lists and reports capabilities, and end with Word for some styles and formatting tips. What you will be able to do as a result: -Become familiar with the Office 2010 navigation and options -Learn new PowerPoint, Excel, and Word techniques that will help you become more effective in creating and managing your documents -Save time on a daily basis About the Presenter: Hope you will be able to join us! Start: 07/12/2012 1:00 pm
End: 07/12/2012 2:00 pm
Why should you attend : Webinar Includes: Q/A Session with the Expert to ask your question PDF print only copy of PowerPoint slides 90 Minutes Live Presentation Description of the topic : In 2010, FDA issued a report on the changes it plans to make to the 510(k) process to address regulatory, industry, and consumer concerns and 2011 and 2012 have been marked by the agency’s progress in implementation of these changes. In the past year, the agency published a draft guidance document that revises and clarifies the agency’s longstanding policies regarding when a new 510(k) submission will be required for changes being made to an existing device and another draft guidance document which creates a second alternate de novo pathway for devices found to be not substantially equivalent (NSE) at the end of the 510(k) process. FDA has also issued a draft guidance document which would change and clarify other aspects of the agency’s 510(k) program in an attempt to foster more consistency across 510(k) reviews, coupled with training and certification for FDA device reviewers. Other 510(k)-related guidance documents have issued as well. Who will benefit: Representatives of manufacturers and marketers of 510(k) medical devices, including in-house counsel, outside FDA counsel, regulatory affairs personnel, and regulatory consultants. About Speaker Mr. Evan P. Phelps is a principal at OFW Law. Mr. Phelps advises companies on compliance with Food and Drug Administration (FDA) law and regulations, with focus on matters related to medical devices and biologics as well as those affecting Clinical Investigators. Start: 07/12/2012 2:00 pm
This one-hour webinar is designed to educate participants on how to guide clients through the process of describing their art work in order to understand patterns of behavior and ways to self-soothe. Full Description: art work. Precise questions to be asked of the client will be provided based on specific art techniques. Participants will be discouraged from imposing their own interpretations on their clients’ art work and will be guided on how to get clients to open up when describing their art- making experiences. This webinar will also provide specific techniques as well as the language needed to describe the directives. In addition, you will learn what questions to ask that will best evoke insight and understanding from the client regarding unconscious motivations, patterns of behavior, and ways to self-soothe. Course Includes: What You Will Learn: Your Presenter: Therapist and Mental Health Counselor and is currently in private practice in Los Angeles, California. Ms. Hayes developed the art therapy program at the Rhode Island School of Design. For the past 15 years, Ms. Hayes has worked in numerous psychiatric settings. Currently, her focus includes families, couples, adults, and children struggling with mood and anxiety disorders, addiction, eating disorders, abuse, and grief- related issues. Ms. Hayes has an undergraduate degree in Fine Arts from Parsons School of Design in New York City and a graduate degree in Marriage and Family Therapy and Art Therapy from Notre Dame de Namur University in Belmont, California. For more information about Ms. Hayes, please visit her website at: www.hayesarttherapy.com Disclaimer: attend. There is no charge for a CCE web account. It is recommended that you join the meeting 15 to 20 minutes early. Speaker phone sound quality is poor and it is recommended that they not be used to listen to the event. Technical requirements: time, you can setup prior to the meeting by following this link: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Pediatricians, Physicians, Art Therapists, Pastoral Counselors, Guidance Counselors, Youth Pastors, Youth Counselors, Educators | ||
