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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: 06/13/2012 10:00 am
End: 06/13/2012 1:00 pm
This training on harassment investigations in the workplace will cover practical steps to conduct effective and legally compliant investigations into harassment, discrimination, or other misconduct allegations/ complaints. Why Should You Attend: When you receive an allegation of workplace harassment, discrimination, or other misconduct, taking prompt and appropriate action is your legal responsibility. However, understanding your legal responsibilities is only half the battle; most of the mistakes in complaint investigations involve the way the parties are treated, what they think is fair, and how the process is communicated and/or implemented. This intermediate to advanced workplace harassment investigation training webinar will discuss, and help you develop, best practices when conducting a legally and psychologically effective workplace probe. In three hours, our expert will help you evaluate the scope of your internal investigation, determine how to document the steps you’ve taken along the way, cover psychologically effective interviewing techniques, and show you how to insulate your organization from a subsequent lawsuit. From fact finding to writing reports, this webinar will cover the do's and don'ts of conducting workplace investigations so you can gain the confidence to be an effective investigator. Start: 06/13/2012 10:00 am
Overview: The U.S. Food and Drug Administration issued the final rule establishing regulations to require current good manufacturing practices (CGMPs) for dietary supplements. The current good manufacturing practices (CGMPs) final rule will require that proper controls are in place for dietary supplements so that they are processed in a consistent manner, and meet quality standards. The CGMPs apply to all domestic and foreign companies that manufacture, package, label or hold dietary supplements, including those involved with the activities of testing, quality control, packaging and labeling, and distributing them in the U.S. The rule establishes CGMPs for industry-wide use that are necessary to require that dietary supplements are manufactured consistently as to identity, purity, strength, and composition. The requirements include provisions related to: the design and construction of physical plants that facilitate maintenance, cleaning, proper manufacturing operations, quality control procedures, testing final product or incoming and inprocess materials, handling consumer complaints, and maintaining records. Dietary Supplement manufacturing sites have been increasingly inspected by the FDA for compliance with the GMPs, and warning letters have been issued. In the face of the increasing scrutiny by the FDA, it is incumbent on dietary supplement manufacturers to understand the regulations and to implement documentation and procedures that will ensure compliance. Why should you attend: The regulations require that you understand the requirements and establish a Quality System designed to meet them. This presentation will review the requirements and the rationale for them. Areas Covered in the Session: \Who Will Benefit: Price List: webinars@globalcompliancepanel.com Phone: 800-447-9407 Start: 06/13/2012 12:00 pm
End: 06/13/2012 1:00 pm
Bryant & Stratton College Online announced today a new session in its ongoing free career training webinar series. Titled “How to Research Companies and Industries,” the free webinar is available to job seekers, prospective students and current Bryant & Stratton College Online students. This session will take place on Wednesday, June 13, from noon to 1:00 p.m. EDT. The “How to Research Companies and Industries” webinar will highlight tips and tricks for job hunters and job interviewees alike on researching potential companies or industries. Attendees of the webinar will learn how to: • Find detailed background information on specific companies, like competitors, hiring practices and current initiatives To register, please visit http://online.bryantstratton.edu/webinar/. Additionally, following the webinar, attendees will be able to download a hand-out recapping the top strategies addressed in the session. Start: 06/13/2012 1:00 pm
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the pharma - it is a good regulation for medical and pharma companies but it is also a good guideline for other industries. Audit Trails play major role in Part 11 compliance - they can be your best friends and/or worst enemies at the same time. Attendees will also receive the below Free documents: - 30+ frequently asked questions (free document) and 21 CFR Part 11 Regulation - PDF Print only copy of PowerPoint slides shared by the speaker. - Q/A session with the Expert Why should you Attend Increase understanding of the Part 11 regulations; improve compliance and meeting the regulations when it comes to different types of audit trails. Description of the topic: Ausir trails are major requirement for many software applications regardless of an industry or users. This is especially true when it comes for Pharma and medical devices companies and other businesses that have implemented or are planning on implementing 21 CFR Part 11 and striving to comply with the same regulation. Areas Covered in the Session: - Subsection of Part 11 and Interpretation of the subsection - Types of audit trails and Strategies of implementing compliant audit trails - Audit Trail Pros and Cons - Audit Trail As an Auditing Tool - Audit Trail Should and Shouldn’t - What if’s? - Commonly asked questions about Audit Trail - What is next about 21 CFR Part 11 Who will benefit: Quality Managers About Speaker Jasmin NUHIC serves a major medical devices OEM as a Sr. Engineer and 21 CFR Part 11 Subject Matter Expert. He also served ASQ section as a chair for two consecutive terms, has taught quality certification exam prep course, completed numerous software validations and obtained over 25 different certifications in leadership, quality, software validations, and more. Jasmin NUHIC has conducted Webinars on this and other topics with high attendance and appreciation. More information about Jasmin NUHIC can be found by visiting his profile on LinkedIn. Start: 06/13/2012 1:00 pm
This one-hour webinar will introduce attendees to the interpersonal dynamics of childhood peer aggression and interventions for victims and aggressors. Current research on treatment and prevention will also be discussed. Full Description: Course Includes: What You Will Learn: Your Presenter: Disclaimer: Technical requirements: Who Should Attend: Start: 06/13/2012 2:00 pm
Is your clinical systems production environment bloated with studies that should be archived? Do you long for an easy way to create and refresh a training environment? Are you struggling with the complexities of migrating studies to a new environment? Does your clinical team desire the power of diagnosing production issues in a test environment without having to involve a database administrator? Look no further. Accel-Copy can do all this and more! BioPharm Systems has developed Accel-Copy to be a versatile tool that allows your clinical environment to be managed by your clinical team more effectively. Out of the box, the application provides the following features and benefits: Database Management: Support and Training Functionality: Clinical Administration and Configuration: Data Quality: The application is fully documented, validated, and GxP compliant. Please join Michelle Engler, the creator of Accel-Copy, for this one-hour presentation that will include a live demonstration of this powerful solution. For more information about BioPharm Systems, visit: http://www.biopharm.com | ||
