Health and Medicine

Course Objectives: To provide to postgraduate microbiologists and infectious disease physicians an updated overview of: * the pathogenesis of intravascular infections including infective endocarditis (IE) and cardiovascular implantable. * electronic device (CIED) infections caused especially by staphylococci and some other pathogens (e.g. Coxiella burnetii). * epidemiology. * improvement of diagnostic clinical and microbiological procedures. * the best imaging techniques for IE and bloodstream infections. * optimized antimicrobial therapy. * antibiotic prophylaxis for IE. * choosing the right animal model for research. There will be two sessions to present and discuss clinical cases with infectious disease experts. Time: 12:00 pm -…

13th International Conference on Advances in Biology, Nursing, Pharmaceutical and Medical Sciences (ABNPMS-18) scheduled on March 19-20, 2018 at Dubai (UAE) is for the researchers, scientists, scholars, engineers and parctitioners from all around the world to present and share ongoing research activities. All accepted papers of ABNPMS-18 will be published in the printed conference proceedings with valid International ISBN number. Each Paper will be assigned unique Digital Object Identifier(DOI) from CROSSREF and the Proceedings of the Conference will be archived in DiRPUB's Digital Library. The Proceeding will be also submitted to SCOPUS/ISI Thomson for review. In addition the proceedings will…

Now in its ninth year, ExL's Proactive GCP Compliance conference continues to act as the annual forum for both senior-level clinical quality and clinical operations executives to gather, learn and discuss strategies to achieve and maintain global GCP compliance. Join us to learn how to effectively build quality risk management approaches into your clinical operations to optimize research, maintain GCP compliance, contain costs and ensure patient safety. Booking: https://go.evvnt.com/186958-0?pid=154 Time: 08:30 to 15:45 Price: Early Bird Pricing - Register by February 2, 2018 - Conference Only: USD 1795, Early Bird Pricing - Register by February 2, 2018 - Conference +…

Training Options Duration: 60 Minutes Monday, March 19, 2018 | 11:00 AM PDT | 02:00 PM EDT Overview: In this session Mr. Wolfe will provide a straight-forward, practical explanation of developing concepts, including the quality and value metrics into new federal health care programs and commercial payment systems, new delivery models, what providers can be doing to develop a value-based strategy, and the application of the Stark Law and other fraud and abuse laws to new models aimed at population health, quality of care and cost control. Mastering these concepts will be a must for health care executives looking to…

Course Objectives: Discuss different aspects related to immunization in adults: - importance and challenges of adult immunization. - immune response in elderly. - vaccine schedule for adults, immunocompromised patients, healthcare workers and travellers. Time: 8:50 am - 4:00 pm. Category: Classes / Courses | Professional Training | Science, Health & Medicine. Sub-Categories: Conferences | Science, Health & Medicine. Prices: Registration Fee EUR for ESCMID members (Full Membership/Young Scientist Membership): EUR 50, Registration Fee EUR all others: EUR 100.

Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? This course delivers the tools, templates, and methods to help participants…

GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations. These applications are, in turn, depended upon a qualified infrastructure that can be relied upon to provide control and regulatory compliance. The consequences of the IT Infrastructure being out of compliance can result in the failure of an entire site or geographic region being brought to a standstill while the compliance issue is resolved. It can also result in regulatory citations during a regulatory inspection as both the infrastructure be out of compliance and also cause the computerized applications that are dependent on…

Cleveland Clinic Abu Dhabi's Internal Medicine Update will take place on 15-17 March 2018 in Abu Dhabi, UAE. The conference will convene over three days where delegates are exposed to the advanced recent developments in internal medicine and medical subspecialties. An outstanding regional and national faculty has been assembled to share advances in their field of expertise. Lectures and discussions will focus on multidisciplinary approaches within Internal Medicine such as Primary Care, Cardiology, Obesity, Endocrinology, Rheumatology and Immunology. Inquiries https://go.evvnt.com/191564-1?pid=154 Price: Standard: USD 400 Speakers: Babak Tousi, Nilam Soni, Michael Knight, Gregory Rosencrance Time: on Thursday March 15, 2018 at…

The 5th Annual Patients as Partners US returns to Philadelphia in March 2018. Patients as Partners is co-produced with patients, industry, academia, government and nonprofit organizations to establish a well-rounded program that addresses the needs of all stakeholders seeking to implement and advance patient involvement across the entire clinical development continuum. PATIENTS INCLUDED ACCREDITED: Patients as Partners US is accredited by Patients Included and addresses what matters most to patients to enable them to support clinical research: 1. Understanding and incorporating the patient's voice in designing clinical trials and developing a clinical endpoint 2. Vastly improving the patient's entire experience…

This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Many companies are outsourcing IT resources and getting involved with Software as a Service (SaaS) and cloud computing. These vendors are not regulated and therefore regulated companies must ensure compliance for both infrastructure qualification and computer system validation. It is the regulated company that wants to avoid FDA form 483s and warning letters. The seminar is intended for regulated companies, software vendors, and SaaS/Cloud providers. The instructor addresses the latest computer system industry standards for data security, data transfer,…

Overview: This is to ensure the quality of the dietary supplement and to ensure that the dietary supplement is packaged and labeled as specified in the master manufacturing record. Why should you Attend: Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), Congress defined the term "dietary supplement", and requires that every supplement be labeled a dietary supplement. Areas Covered in the Session: Required steps for CGMP compliance Problem areas, common pitfalls Implementation:Systems,templates and tools Who Will Benefit: Senior Management in Dietary Supplements Industry QA/RA R&D Engineering Marketing Consultants Speaker Profile: John E. Lincoln is a medical device…

Training Options Duration: 60 Minutes Tuesday, March 13, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar for HIPAA Covered Entities and Business Associates explains how to use the HIPAA Rules to Prevent, Prepare, Respond and Recover from Cyber Attacks. Why should you Attend: Cyber Threats to the Security of Health Information are at Crisis levels. The latest threats are caused by two security flaws called "Meltdown" and "Spectre" in nearly all "chips" - microprocessors installed in electronic devices like computers, smartphones and tablets. Windows, Linux, iOS, MacOS, tvOS, Android and nearly all operating systems are affected…

Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? This course delivers the tools, templates, and methods to help participants…

OVERVIEW FDA and U.S. Customs and Border Protection are using new import requirements.The FDA’s import software screening program (PREDICT) and the U.S. Custom’s ACE software program require more information from the foreign source(s). FDA’s product codes and U.S. Harmonized Tariff Schedule (HTS) link the requirements. Take away is that the software coding information must be correct. Otherwise, you face costly delays and possibly a refusal of the entry. In addition, information on the entry’s commercial or pro forma invoice must be consistent with the information entered into PREDICT and ACE software. All products regulated by the Food and Drug Administration…

MAIN TOPICS: Resuscitation Oxygen And Ventilation Infections High-Tech Monitoring Nursing Ventilation ORGANIZING COMMITTEE: Paolo Biban Urls: Tickets: https://go.evvnt.com/184765-1?pid=154 Twitter: https://go.evvnt.com/184765-2?pid=154 Facebook: https://go.evvnt.com/184765-3?pid=154 Price Physician: EUR 350 Nurse: EUR 250 Abstract Submitter: EUR 250 Time: 8:45 am - 5:00 pm

Training Options Duration: 60 Minutes Friday, March 9, 2018 | 11:00 AM PST | 02:00 PM EST Overview: In this webinar Mr. Wolfe will discuss emerging governance structures, reporting and documentation requirements, approval processes, and other developing best practices in the industry to help attendees appropriately engage their board and/ or compensation committees in oversight. Why should you Attend: In this webinar Mr. Wolfe will explore the expanding role of boards and committees in physician compensation oversight, in decision-making and in day-to-day policy and process implementation. Areas Covered in the Session: Guidance on Board Fiduciary duties and Responsibility for oversight…

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors. The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a "Cleaning Validation Master Plan"…

This two day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates. The second part of the first presentation is an overview of how to manage the HIPAA compliance project. At the end of these presentations there will be a workshop…

Course Objectives: * To highlight the initiatives for monitoring migrants' health, prevent and control infectious diseases in migrants in GCC and EMRO. * To discuss the impact of migrants on the health systems of the hosting countries especially for vaccine preventable diseases, importation of communicable diseases and AMR. * To present the ways to enhance GCC/EMRO preparedness for infectious diseases in migrants during peace and conflict. * To highlight the importance of intergovernmental and international organizations collaboration required to address migrants' health needs in GCC/EMRO. * To discuss the role and impact of migrants on the elimination programs for TB,…

Overview: This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome. Why should you Attend: In December 2010 the FDA changed the way it does audits to include 21 CFR 11 add-on inspections. Very little is known about this, yet the FDA has already issued citations on the subject. Areas Covered In the Session: What is FDA's…