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: 06/07/2012 9:00 am
End: 06/08/2012 4:00 pm
Course Description: This 2-day on-site Course will help you gain a comprehensive understanding of the Regulatory Structure, Clinical Trial Requirements and the Conduct of Running Clinical Research in Japan and South Korea. It will prepare you for the regulatory approval processes, Agency meetings, the complexities of running studies in both countries, the importance of partner selection and the cultural knowledge needed for success. The recent changes made by PMDA and KFDA to be more sponsor-friendly will be reviewed. Real world experiences on actual interactions with the Agencies since these changes, will also be discussed. Who will Benefit: This course will be beneficial to the following personnel whose responsibilities require knowledge of Japan and South Korea's regulatory requirements for Life Science products:
Start: 06/08/2012 10:00 am
End: 06/08/2012 1:00 pm
This 3-hr virtual seminar will focus on the basic tenants of the laws surrounding EEO and what that means for your management practices. It will provide a comprehensive overview of employment law, key legislation affecting your management decisions and your responsibility to understand and comply with it. Why Should You Attend: For many, EEO is regarded as management’s worst nightmare and Federal, state, and local legislation is often cited by many emerging firms as one of the major barriers to growth. This may be because of the known consequences for not complying. Unfortunately though, actually managing the human resource of the organization is a discriminatory activity. Decisions have to be made on whom to hire, fire, promote, give pay raises, etc. It is when these decisions are not made according to Equal Employment Opportunity requirements that a company may find it has problems with illegal discrimination. In this three hour virtual seminar, we will overview employment law and the principles on which it is based so that leadership can be provided with the necessary tools to develop sound policy and provide interpretation and recommendations on a wide range of EEO and civil rights issues to individuals within the organization. In this first of four segments on the subject, the attendee is provided with essential information on the tenants of EEO and common misconceptions about compliance. Learning Objectives: Upon completion of this summit, the participant will be able to:
Start: 06/08/2012 10:00 am
End: 06/08/2012 11:00 am
This webinar will help you understand the significant differences between qualification and validation of an analytical method, the expectations and requirements of each, and their place in the analytical method lifecycle. Why Should You Attend: Execution of a method validation is a resource intensive activity, both in terms of manpower, equipment usage, time, and money. The more the process is well defined and understood, the greater the potential for an efficient project. The less the process and its elements are understood, the greater the chance for delays and additional resource expenditures. There is confusion and a lack of guidance over what constitutes a method qualification compared to a method validation, and what are the requirements for different phases of validation, what is needed at each product phase (I,III,commercial), and what to do when there are failures within a validation. Inclusion of a CRO as an additional factor in this plan potentially escalates areas that need resolution-differences in quality systems, validation requirements, and reports to name a few. Communication without common definitions and understanding of the terms can lead to areas of confusion, project misdirection, and missed timelines. Learning Objectives: Areas Covered in the Seminar:
Start: 06/08/2012 10:00 am
End: 06/08/2012 11:30 am
This 90-minute webinar will clarify your confusion about Test Article Characterization for GLP drug studies. You will learn the correct way to use GMP characterization data in a GLP study, understand how to characterize a medical device as a test article, learn the common mistakes made in test article characterization and the basic requirements for drug and device stability testing. Why Should You Attend: The presentation will begin with a review of GLP requirements for test and control article characterization, regardless of whether the article is a drug or device. It will address the study director's responsibilities and sponsor responsibilities in test article characterization. Attendees will learn the best practices for managing GMP characterizations, stability, and certificates of analysis. Special attention is given to the testing that must be performed to show that no test material carried over into control materials. Carryover has become one of FDA’s target areas in recent years because of the serious effect it has on drug safety results. The presentation treats carryover as a special topic in test article/control article characterization. The presenter also emphasizes the importance of control article characterization. The presentation then covers the unique aspects of medical device characterization and stability testing. This discussion describes how device design planning and development fit into characterization. The webinar also covers combination products, how to identify what makes up the test article, and then the testing to show stability and characterization. This section is followed by a discussion of stability testing in general as it applies to characterization. Areas Covered in the Seminar:
Start: 06/08/2012 11:00 am
Untreated depression in children and adolescents can lead to more serious episodes of depression during adulthood. Drug choice and length of treatment can make a significant difference is the lives of your youngest patients. Full Description: Course Includes: What You Will Learn: Your Presenter: Disclaimer: Technical requirements: Who Should Attend: Start: 06/08/2012 1:00 pm
Oppositional Defiant Disorder doesn’t have to be complicated! This web course provides mental health professionals with a three-step approach to treating the signs and symptoms of ODD and co-occurring disorders in children and teens, ages 4-14. Full Description: ultimately the therapist and child. Tantrums, arguing, defiance, blaming, and anger when left untreated may disrupt classrooms, strain families, and lead to a risk of juvenile delinquency. Conflict may also go on to affect the behavioral, academic, and social success of the child. adolescents as well as educate parents to reinforce good behavior to maintain success. Course Includes: What You Will Learn: Your Presenter: Work from Syracuse University and a master’s degree in education from The College of Saint Rose. Mr. Halverson currently runs an outpatient mental health private practice where he specializes in the treatment of child and family defiance, anxiety, and trauma, and has developed the SimpleThree system to approach these issues with his clients as well as other mental health professionals. Disclaimer: 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: https://apidemoeu.webex.com/apidemoeu/meetingcenter/mcsetup.php Who Should Attend: Professionals, Parents, Clergy | ||
