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: 06/14/2012 9:00 am
End: 06/15/2012 4:00 pm
Course Description :- Sterilization is a critical aspect of device approval and release. Though this is indeed fact, manufacturers sterilize product as a matter of course, without expert sterilization assurance personnel to guide them through potential problems in sterilization. As the world and meaning of CAPA continue to evolve in the medical device industry, further misunderstanding arises when faced with determine root cause and corrective (or preventive) action for any variation in this critical process in device manufacture. The course will begin with an overview of EO sterilization, explaining which aspects of the process often cause confusion. This will be followed by process validation and what paperwork is required to provide ‘documented evidence’ ; and finally what are typical deficiencies encountered in the EO process. Next a detailed explanation of Radiation Sterilization will be given. Specific to Radiation Sterilization is the required sterilization dose, which will be covered in depth – how to determine sterilization dose and how to maintain the validated dose. Process validation will be covered as well as the typical deficiencies encountered in Radiation Sterilization and Validation. Critical and non-critical deficiencies will be covered and when this should trigger a CAPA. Finally contract sterilization will be reviewed with the specifics of how to deal with CAPA when you are not directly responsible for sterilization. Who will Benefit:- This course will be beneficial to the following personnel in Medical Device Manufacturing and Sterilization facilities:
Start: 06/15/2012 10:00 am
End: 06/15/2012 11:00 am
Don't Be Caught in the 20th Century Rut… Attend this free, live webinar to learn how to make the transition from live events to online events - painlessly. During This Webinar You Will Learn How To: All Registrants Will Receive: If you can't attend the webinar, register anyway, and we will send you a link to a free replay. About the Presenter: Start: 06/15/2012 10:00 am
End: 06/15/2012 11:30 am
This 90 minute webinar will help you comprehensively understand the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an FDA IND Application. Why Should You Attend: All sponsors, CROs, Sites and auditors of Clinical Research who are involved in pharmaceutical or biological development need to possess the knowledge and be efficient in completing successful applications for their studies. Knowing what is expected of you and “getting-it-right” the first time, will allow faster development of innovative products. This 90 minute training course will provide your company the opportunity for comprehensive understanding of the IMPD (Investigational Medicinal Product Dossier) and the structure and content differences between a EU CTA Application and an FDA IND Application. Additionally, this webinar covers many related processes sponsors will need to know, as they file for, conduct and close-out effective clinical studies in the U.S. and EU. Agenda: (All time in EDT):
Start: 06/15/2012 10:00 am
End: 06/15/2012 11:30 am
This 90-minute webinar will help you understand what the true costs are for completing a clinical study and the unanticipated costs that may arise. You will learn about costs that a sponsor must include in a budget and costs that a site bears in the conduct of clinical research. Determining an appropriate clinical trial budget to ensure a study can be completed is challenging for both sites and sponsors. Whether you are new to clinical research, or have years of experience, there are 3 areas of expertise you may not have mastered - understanding and outlining costs, negotiating budgets, and complying with criteria (Medicare provisions for determining Qualifying Trials and Routine Care). If not, you may be a site that is underwriting sponsors costs, or you may be a sponsor that is overpaying site costs, and both sites and sponsors may be incorrectly submitting non-qualifying costs to insurers. This webinar is intended to provide comprehensive terms of expenses and steps for evaluating costs; tips for negotiating budgets; and key information on determining qualifying trials and routine care. In addition to learning how to create complete and detailed cost plans and learning all terms are in fact negotiable, learn how to protect clinical research billing by keeping it compliant. The instructor’s extensive knowledge and experience in ensuring appropriate clinical trial billing to third party insurers (including federal, state and private) makes her well suited to answer your questions and offer best practice guidance to avoid errors in billing. Start: 06/15/2012 1:30 pm
Is it really possible to provide “End user customizable” business rules and workflows in a multi-tenant .NET application with a single code base? How can we do this without compromising on development time flexibility, run time performance, cloud ready architecture and scalability? Techcello will be hosting a webinar on this topic: Friday June 15th 1.30 PM US EDT Register : https://www1.gotomeeting.com/register/124103232 Thursday June 14th 3 PM BST (UK) Register : https://www1.gotomeeting.com/register/652000993 For more information : http://blog.techcello.com Start: 06/15/2012 2:00 pm
This webinar is designed to educate participants about art therapy and provide practical skills for effective assessment and intervention with clients experiencing symptoms of anxiety. Full Description: clients experiencing symptoms of anxiety. Demonstrations of art therapy techniques will advance the participants’ understanding of the bio psychosocial perspective of many of the disorders that fall under the category of “anxiety,” including phobias, PTSD, panic, as well as sleeping and eating disorders. Significant attention will be paid to treatment interventions with numerous opportunities for hands-on art-based techniques. Course Includes: What You Will Learn: Sleep Disorders, and Panic Attacks 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 | ||
