Health and Medicine

Product Format: Live Webinar Presenter(s): Dr. David Lim, Ph.D., RAC, ASQ-CQA Conference Date: Tuesday, April 3, 2018 Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Duration: 60 minutes Price: $227.00 Join this session with expert speaker Dr. David Lim and learn how to adequately develop and implement Excel spreadsheet computer system validation in your organization in compliance with FDA’s 21 CFR Part 11. You will get in-depth insights to improve your awareness in order to better implement Part 11 and computer system validation requirements to avoid citations in 483s and warning letters.…

Product Format: Live Audio Conference Presenter(s): Toni G. Cesta, Ph.D., RN, FAAN Conference Date: Tuesday, April 3, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 60 minutes Price: $227.00 In this session, industry veteran Toni G, Cesta will help you understand how to maintain compliance in a variety of areas directly related to utilization management and discharge planning. You’ll learn how to survive Joint Commission and CMS audits that are scrutinizing hospitals’ and case management departments’ compliance with the Conditions of Participation and other regulatory requirements. For Registration, visit…

OVERVIEW Part 1 QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025: The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. What is also needed are the “how to do it” or procedures and methods and finally the controls or evidence that it was done properly. This is the 1st of two webinars on…

The FDA is increasing its enforcement actions both for domestic and foreign inspections. Enforcement statistics have not been summarized yet because 2017 has not ended yet. We are certainly seeing more Warning Letters and Import Alerts based on Data Integrity (21 CFR Part 11: Electronic Records; Electronic Signatures. In the past FDA used to issue several Warning Letters to the same firms upon consecutive inspections. Today, after receiving one Warning Letter the next regulatory action is elevated to Import Alert, Consent Decree, and Injunctions for domestic manufacturers. Senior Management must take the initiative in setting the tone of full compliance:…

Being the HIPAA Security and Privacy Official involves not only ensuring you know the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited or the subject of a breach investigation, you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the fundamentals of a HIPAA compliance program. If your HIPAA Security and Privacy Official needs to understand what…

Overview: An overview of the history of Data Protection within the EU and introduce you to the enhancements and new obligations imposed by the EU GDPR. Why should you Attend: Attendees will learn the common EU rules that have been established to ensure that personal data has a high standard of protection across the EU. Attendees will also learn about their rights to complain and obtain redress if their data is misused in any of the EU member states. Areas Covered in the Session: How EU Data Protection Regulation affect social networks How EU Data Protection Regulation benefit existing European…

The Dubai International Neuroscience Congress is designed to cover the latest approaches in Neuroscience and current updates on management and treatment in different areas. Dubai International Neuroscience Congress taking place 29-31 March 2018 in Dubai, UAE. The programme is designed to cover the latest contemporary approaches in Neurology and current updates on management and treatment in different areas; mental disorders, schizophrenia, Alzheimer, bi polar disorders, adult eating disorders, and many more... The congress will feature interactive case-studies, platform presentations, meet the expert sessions, educational workshops, networking sessions and more, to provide a comprehensive review of current issues and recent advances…

Training Options Duration: 60 Minutes Wednesday, March 28, 2018 | 11:00 AM PDT | 02:00 PM EDT Overview: In this session Mr. Wolfe will provide an overview of the Stark Law, including its technical requirements and key tenets of defensibility. He will also discuss best practices for structuring evaluating and structuring new compensation models. The webinar will focus on regulatory requirements, key provisions, valuation considerations and potential pitfalls that should be avoided. Why should you Attend: As health care organizations redesign their compensation plans, they must be sure the process they follow and the models the new models they develop…

Product Format: Live Audio Conference Presenter: Melissa Abbott, RN, MSN/MHA Conference Date: Wednesday, March 28, 2018 Aired Time: 1:00 pm ET | 12:00 pm CT | 11:00 am MT | 10:00 am PT Length: 90 minutes Price: $197.00 Join expert speaker Melissa Abbott, RN, MSN/MHA for an information-packed educational session and learn how to boost your home health agency’s outcome measures in 2018. Melissa will show you how to understand your CASPER reports and Star Ratings by peeling back the layers of jargon to reveal how these reports tie back to real-world home healthcare practices. This session will not only…

Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management. To comprehensively summarize all risk related activities and to demonstrate the safe…

This conference will be focused on analyzing and discussing the best practices and strategies for those preparing for audits and inspections. - Pharmacovigilance/Drug safety (QPPV) - Regulatory Affairs - Quality and Compliance - Medical Information - Risk Management - Compliance - Pharmacovigilance Auditors - Management Staff Responsible for Running Inspections - Employees (directly and indirectly) Involved in Inspections - Drug/Product Safety - Drug Development - Information and Clinical Data Management - Clinical Pharmacology - Clinical Safety - Research & Development - Quality Assurance - Patient Safety - Signal Detection - Safety Surveillance - Outcome Research - Data Analysis - Epidemiology…

This conference will be focused on analyzing and discussing the best practices and strategies for those preparing for audits and inspections. - Quality and Compliance - Medical Information - Risk Management - Compliance - Pharmacovigilance Auditors - Management Staff Responsible for Running Inspections - Employees (directly and indirectly) Involved in Inspections - Drug/Product Safety - Drug Development - Information and Clinical Data Management - Clinical Pharmacology - Clinical Safety - Research & Development - Quality Assurance - Patient Safety - Signal Detection - Safety Surveillance - Outcome Research - Data Analysis - Epidemiology - Medical Affairs - Regulatory Affairs and…

The Organizing Committee of the International Scientific and Practical Conference of the Open European Academy of Social Sciences (Spain, Barcelona), in partnership with the University of Barcelona (Spain, Barcelona), the University of Berlin (Germany, Berlin), invites you to participate in the event. The collection is indexed in international databases of scientific works, assigned to the DOI. The copies of the collection of the conference are sent to the book depositories and catalogs of the Universities of Barcelona and Berlin. The materials of the collection are published in printed and electronic form and sent to the authors. The certificate of participation…

The Organizing Committee of the International Scientific and Practical Conference of the Open European Academy of Social Sciences (Spain, Barcelona), in partnership with the University of Barcelona (Spain, Barcelona), the University of Berlin (Germany, Berlin), invites you to participate in the event. The collection is indexed in international databases of scientific works, assigned to the DOI. The copies of the collection of the conference are sent to the book depositories and catalogs of the Universities of Barcelona and Berlin. The materials of the collection are published in printed and electronic form and sent to the authors. The certificate of participation…

Steps to increase Wellbeing - Want to Start Up a Business in 2018? - Ideas for Green thinkers This exciting event in Hove is the place to be for all of you wanting to get off to a flying start with RINGANA in the UK. Spend an hour with us - RINGANA - Winner of the 2017 European Business Award - (Chairman's Award) - and learn how And why we are growing annually at over 40-50% and how you can join our successful Green Business and build a potentially properous future. A unique opportunity with an award winning company -…

This course will start with an introduction to the different types/phases of clinical trials. The different types are intended to test for the safety and efficacy of the treatment in question. The key document in any clinical trial is the study Protocol. The general contents of this document are specified in the FDA Regulations - Code of Federal Regulations (CFR) section 21. This document is key to everything that goes on during the trial. It is recommended that if you have anything to do with the trial you should review this document. During a clinical trial there can be a…

MAIN TOPICS: - Infezioni e vaccinazioni - La medicina perinatale nei migranti - La gravidanza gemellare - La prematurita ORGANIZING COMMITTEE: - Irene Cetin - Nicola Chianchiano - Angela Motta URL: Booking: https://go.evvnt.com/186694-1?pid=154 Prices: Physician: EUR 300.00 SIMP member: EUR 200.00 Nurses, Obstetricians: EUR 150.00 Students: EUR 0.00 Speakers: Prof. Irene Cetin, Prof. Angela Motta, Prof. Nicola Chianchiano Time: 9:00 am to 8:00 pm

The Adaptive Clinical Trials Symposium, taking place March 22-23 in Philadelphia, will educate cross-functional stakeholders on the importance of statistics, data management, and operations to improve clinical performance. Last year, our Interim Analysis Symposium provided attendees with knowledge of best practices to enhance the capacity at which organizations can produce accurate reports to expedite products to market. This year, in response to industry trends and changes, we expanded our reach to encompass all that is adaptive design. Our goal is to inform those involved about how the adaptive design allows for a more proficient use of capital and resources through…

The AACC Middle East has been designed to provide a comprehensive overview of selected relevant topics in the
eld of clinical laboratory medicine presented by renowned international and national speakers. The AACC is considered a great chance for the attendees to update their knowledge, stimulate collaboration with each other’s and exchange experiences with distinguished line-up of experts. The AACC 2018 Abu Dhabi is expected to be an exciting venue to hear and discuss the latest scienti
c advances in all disciplines pertinent to the
eld of laboratory medicine including laboratory quality management and accreditation, clinical chemistry, newborn screening, genetics, oncology and…

10th International Conference on Chemical, Biological, Environmental and Medical Sciences (CBEMS-18)) scheduled on March 21-22, 2018 at Istanbul (Turkey) aims to bring together leading academic scientists, researchers and scholars to exchange and share their experiences and research results about all aspects of Chemical, Biological, Environmental and Medical Sciences and discuss the practical challenges encountered and the solutions adopted.