Events
| Fri | ||
|---|---|---|
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: 07/19/2012 9:00 am
End: 07/20/2012 5:00 pm
Course Description :- Most medical devices marketed in the European Union must follow the Medical Device Directive (MDD); IVD device and active implantable devices have other directives. The MDD can be complicated, especially for US companies, because the MDD’s approach is different than the regulatory approach in the US. For example, under the MDD your company makes “submissions” to a private company that you hire, not to a government agency. This interactive two-day course will help you comprehensively understand details of the MDD and implement its requirements. Attendees will learn how to classify devices, select the appropriate conformity assessment path, prepare the required documentation, and maintain it. During the course, participants will have exercises that apply the principles and help solidify learning. The instructor addresses the details of the MDD and includes other significant issues such as the Quality Management System (ISO 13485), Risk Management (ISO 14971), Clinical Evaluation (MDD Annex X), and the role of harmonized standards. Course Objectives :-
Start: 07/20/2012 10:00 am
End: 07/20/2012 11:00 am
Whether you are looking to earn non-dues revenue or create an additional income source, offering paid webinars is an easy way to profit from your knowledge. This webinar explores ways to convert your valuable, industry-specific knowledge into something tangible – and profit from it. What You Will Learn: Who Should Attend: All Attendees will receive: a copy of "Costs of Putting Together a Webinar” Join us for this free webinar. If you're not able to make it to the webinar, register anyway! We'll share a recording after the event. Start: 07/20/2012 10:00 am
End: 07/20/2012 11:00 am
This webinar will identify some of the incorrect lore attached to liquid chromatography and will consider HPLC from a multi-dimensional point of view. It will expand your awareness of fundamental chromatographic phenomena rarely discussed in academic courses so that more informed, efficient, and effective choices can be incorporated into the development effort. Why Should You Attend: In the dog-eat-dog world of pharmaceutical development, time is the factor of greatest concern to management. The temptation to rush through development without fully understanding chromatographic phenomena frequently leads to the validation of methods incapable of quantitation, specificity, or even correct identification. This webinar will point out some of the errors in understanding and judgment that lead to such catastrophes, and will provide sound bases for the evaluation of method suitability. With a solid understanding of the fundamental principles outlined in the presentation, participants will be able to meet even the most demanding expectations for development timeline without sacrificing method requirements or quality. The information in this presentation will allow you to understand chromatography as you never have before. Because of the nature of pharmaceutical work, the knowledge offered in this course may prove critical to the success of development efforts. Chromatographers who employ these ideas will become more efficient and will be less likely to commit some of the errors that are common to our industry, allowing themselves and their companies to excel. Learning Objectives: The objective of the course is to expand participants’ awareness of fundamental chromatographic phenomena rarely discussed in academic courses so that more informed, efficient, and effective choices can be incorporated into the development effort. Start: 07/20/2012 10:20 am
End: 07/20/2012 11:30 am
This 90-minute webinar will provide you a thorough understanding of the updated framework surrounding Good Pharamcovigilance Practices (GVP) in the EU. This will include updates to the EU regulation, Directive and the first seven PV Modules, which have been published for consultation. Why Should You Attend: This webinar is focused on understanding the new requirements for Good Pharmacovigilance Practices that will begin to become effective in the European Union beginning July 2012. The New Guidance on Good Pharmacovigilance Practices (GVP) has been updated by Module, of which the first seven Modules have been disclosed for public consultation. This course will describe the Regulatory Updates, Guidance Updates and thoughts on how some Member States’ Competent Authorities will proceed with implementation. These regulatory changes will also impact the EU Clinical Trial Directive and expectations of sponsors in the protection of patients and public health, before, during and after a clinical study. Key Topics to be Discussed: - Pharmacovigilance systems Start: 07/20/2012 11:00 am
Cloud Computing has been a hot topic and the word "Cloud Computing" has been used lot more often, but what is "Cloud Computing" and why you should learn more about it? To know more about Cloud Computing and to explore the challenges and opportunities that it presents, take a few minutes to attend this webinar. | ||
