Education

Overview: This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/usability validation. Why should you Attend: We will explain how to choose the tests to be conducted and the studies that must be completed prior to the actual validation test. The post test participant inquiry is critical to validation success. we will describe how to do this. Areas Covered in the Session: Required number of Participants Test Procedure Qualitative Success Criteria Choice of Tasks to Validate Post test Participant Inquiry Who Will Benefit: Engineer Engineering Manager Regulatory Personnel QA Speaker Profile:…

Overview: Why DMFs are important to you and your company , and How DMFs fit into FDA's regulatory processes for review of drug and biologic applications. Areas Covered in the Session: Why DMFs are important to you and your company How DMFs fit into FDA's regulatory processes for review of drug and biologic applications Why, more than ever, you may need DMFs to maintain current supplier agreements as well as to develop new business relationships What not to include Who Will Benefit: Manufacturing Regulatory Affairs Project Managers Global Supply Chain Research and Development Quality Assurance & Control Speaker Profile: Robert…

Premier Publishing s.r.o. (Austria-Czech Republic) invites you to participate in the III International Conference on Education and Applied Psychology, which will be held in Vienna on April 15, 2018. The conference will be conducted in distance way without necessity of personal presence. We invite students and postgraduate students, postdoctoral students, employees of educational institutions, without regard to the country of residence, to participation in the conference. Articles for the conference proceedings are accepted till April 14, 2018 inclusive. Working languages: English, German, Russian, Ukrainian. Example of output data of an article: Mark, Smith. New approaches to applied psychology // Proceedings…

,!U¾n†“Connect MBA”¯‚¥ ïåê?Ûe[ b—FfbÛ˜ùb„:÷(¥ önÝþ “Â  Connect MBA D^;¨” Speakers: GMAC Time: 1:00 pm - 6:00 pm

Course "The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities…

CANADA'S LARGEST MONEY-MAKING EXPO Self-Made Millionaires Teach You How To Make Money! Who You'll Meet: Hollywood Icon Sylvester Stallone; baseball legend, Alex Rodriguez, Shark Tank's Daymond John, Dragons' Den's Manjit Minhas; HGTV's Love It or List star Hilary Farr, Million Dollar Listing LA's Madison Hildebrand; Top Million Dollar Agent's real estate brokers Mike Donia & Jin Jiang; Home To Win's Sebastian Clovis, best-selling author of UNFU*CK YOURSELF Gary Bishop, and a special LIVE performance by Pitbull. You'll Learn: - Sales and peak performance training. - To flip properties; strategies to increase your income. - To find a home-based business that…

Overview: GMP regulations describe required quality management system for production and testing of products in these regulated industries. The purpose of the GMP regulations is to ensure that a product is safe and meets its intended use. Why should you Attend: Learn about GxP/GMP regulations and how they affect quality management system and quality audit. Learn about different types of quality audits and how to properly prepare for them, what actions you need to take to ensure that your organization will pass an audit. Areas Covered in the Session: GxP/GMP Framework Quality Management System Quality Audit Who Will Benefit: Quality…

Course "A Risk Based Strategy for the Development & Validation of and Validation of Analytical Methods with a QbD Approach" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Following the initial development, the steps further continues thru optimization and subsequently to Validation, leading to the understanding of Validation Parameters and their generic definitions. Guidance from EP, USP, ICH Q2 (R)1, AOAC etc. will be discussed. The presentation continually builds on from a conceptual level to practical applications leading to data handling, Data Integrity, Validation Protocol and other…

Overview: How to conduct a software validation program that will satisfy FDA requirements and produce a safe product. Why should you Attend: There are additional requirements,analyses and tests that FDA feels are necessary to prevent user injuries. These requirements were developed after analysis by the FDA of many recalled medical devices. In this webinar you will learn the requirements in addition to functional tests that are required to produce a validated software product. Areas Covered in the Session: Software Validation more than Testing Requirements Traceability Risk Analysis Unit,Integration and System Testing Algorithm Validation Challenges to the Software Configuration Management Who…

Overview: This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more. It will also address major changes under the Omnibus Rule and any other applicable updates for 2018 and beyond. There are an enormous amount of issues and risks for covered entities and business associates these days. I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain…

Overview: This is an interactive overview of how DMAIC can be utilized in a home environment to improve the quality of life for a child diagnosed as being on the Autism Spectrum. Why should you Attend: The same tools and skills can be applied to any other form of personal or professional issue. This session rated first at the ASQ WCQI conference when it was presented there. It leaves people motivated and refreshed with a plan of how to manage systems with a toolkit that they can easily apply. Areas Covered in the Session: To help people understand how lean…

Accelerate your team's understanding in designing, implementing and monitoring critical KPIs using powerful performance dashboards

Acquire change management skills essential for a business environment by attending this training program.

Understand US Pharmacopeia General Chapter 1029 and all aspects of GDP including practices for writing and correcting documentation

Learn practical Excel fundamentals to improve the accuracy and efficiency of payroll production by attending this webinar by David H. Ringstrom

Learn the key steps to coaching employees on performance or on behavioral issues. Learn some coaching models to improve direct report performance

Learn to utilise the features of Power Pivot and Query to summarise large amounts of data and streamline the process of presenting the results

Learn how to define your workweek, what is compensable working time, how to determine the regular rate of pay, more by attending this webinar

Learn how to utilize export audits to assess the effectiveness of current export compliance processes and check for inconsistencies in day-to-day operations

The idea of 8th International Conference on Languages, Education, Humanities and Social Sciences (LEHSS-2018-LONDON) scheduled on March 28-29, 2018 London (UK) is for the researchers, social scientists, scholars, engineers and practitioners from all around the world to present and share ongoing research activities. This conference provides opportunities for the delegates to exchange new ideas and application experiences face to face, to establish business or research relations and to find global partners for future collaboration. All accepted papers of LEHSS-2018-LONDON will be published in the printed conference proceedings with valid International ISBN number. Each Paper will be assigned unique Digital Object…