Health and Medicine

The Medicine Unit of ATINER organizes a Stream on “Shifting Diabetes Education and Prevention Program from Specialized Diabetes Centers to Community Structure” as part of the 4th Annual International Symposium on Diabetes, 7-10 May 2018, Athens, Greece sponsored by the Athens Journal of Health. The rapidly world-wide growing frequency of diabetes, engulfing children with development of disease complications earlier than before, and the failure to achieve satisfactory glycemic control and prevention of secondary complications, despite huge efforts and investments, indicate an urgent need for a different approach toward diabetes management. We would like to present our work using a novel…

9th International Conference on Food, Waste Management, Cellular and Molecular Biology (FWCMB-18) that will be held during May 7-8, 2018 Dubai (UAE). The primary goal of the conference is to promote research and developmental activities in Food, Waste Management, Cellular and Molecular Biology. Another goal is to promote scientific information interchange between researchers, developers, engineers, students, and practitioners of different parts of the world. The conference will be held regularly to make it an ideal platform for people to share views and experiences in Agricultural, Biological, Environmental and Medical Sciences as well as in related fields. The proceedings of the…

This conference is the latest event in our Drug Discovery Series and the sister event the European Precision Medicine Summit. Attendees will have the opportunity to hear from an excellent panel of experts within the field and learn, share and observe from a range of exhibitions and presentations on companion diagnostics, biomarkers, immuno-oncology, liquid biopsies, AI and other facets of precision medicine. This two-day summit features over 48 contributions & four interactive tracks will explore strategies and technologies to deliver precision medicine, biomarkers in clinical & translational development, companion diagnostic partnerships & development and Immuno-Oncology.

Exhibitor Opportunities are available. Please contact the Conference Manager. The 2018 Primary Care Hawaii Conference - Caring for the Active and Athletic Patient (PCC) at the Grand Hyatt Kauai Resort May 7-11, 2018 promises to be one of the best educational opportunities for physicians and medical professionals who care for active and athletic patients or who themselves lead such a lifestyle. Register today to join us at the fabulous Grand Hyatt Kauai Resort for this unique conference The curriculum is directed to Family Medicine, Internal Medicine, Pediatrics, Emergency Medicine, PM&R and Orthopedics specialists as well as Physical Therapists, Athletic Trainers,…

This conference is the latest event in our Drug Discovery Series and the sister event the European Precision Medicine Summit. Attendees will have the opportunity to hear from an excellent panel of experts within the field and learn, share and observe from a range of exhibitions and presentations on companion diagnostics, biomarkers, immuno-oncology, liquid biopsies, AI and other facets of precision medicine. Website https://go.evvnt.com/187115-1?pid=154 Twitter https://go.evvnt.com/187115-2?pid=154 Prices: Industry Fee: USD 1499.00 Academic/Hospital/NFP Fee: USD 599.00 Solution Provider Fee: USD 1899.00 Time: on Monday May 07, 2018 at 9:00 am (ends Tuesday May 08, 2018 at 5:00 pm)

2018 Highlights We are pleased to welcome Jim Roach, MD, CMO, Pulmatrix as co-chair of the CMO Summit for the first time. Also joining the Summit for the first time is Azmi Nabulsi, MD, CMSO, Head of R&D Strategic and Professional Affairs, Takeda Pharmaceuticals who represents the CMO, large pharma perspective. Ken Getz, Director of Sponsored Research Programs, Tufts CSDD, delivers his annual keynote on discussing Key Trends in the R&D Landscape. New for 2018: - How is the Shifting Biotech Life Cycle Changing Clinical Partnerships with Big Pharma and the Role of the CMO? - Finding the Common Ground…

Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…

Training Options Duration: 60 Minutes Monday, May 7, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: We will review the various elements of the physician employment agreement, focusing on the pitfalls and the problems that can develop when the agreement does not clearly define the relationship, and/or when the parties do not fully understand what is being agreed to. Such items as term and termination, termination for cause, duties of the physician, call, non-compete, and compensation are all items that should be clearly set out in the agreement and fully understood by the parties. Why should you Attend:…

Back by popular demand, CMHC brings you the 2018 CMHC West: Advancing Cardiometabolic Health from East to West in Las Vegas, NV, May 4-5, 2018. CMHC West will capture the integrity and high-quality education of the annual Cardiometabolic Health Congress as the nation's top experts in cardiometabolic health will highlight the latest updates in hypertension, heart failure, diabetes, lifestyle management, and cardiovascular health. The most recent results from top-line clinical trials and new and emerging agents will be brought to you through thought provoking and innovative education. Invest in your education and the health of your patients by attending CMHC…

Overview: The premise behind RBQM is that monitoring quality can be improved by leveraging existing data intelligence. This, in turn, calls for more robust quality assurance (QA) systems focused and efficient resource utilization and allocation at the clinical site level. Why should you Attend: Practical aspects of developing relevant Key Performance and Quality Indicators (KP-QIs) for Risk-Based Quality Management will be discussed. Areas Covered in the Session: Identify and manage risks of clinical trials Perform Cause-Effect Anaylysis for identified risks and develop mitigation strategy Review recent noncompliance trends and regulatory focus for Sites, Sponsors, and IRBs Develop effective Corrective Action…

The course is designed to review critical elements of the new regulations and is suitable for clinical, regulatory and quality leaders. The course is suitable to anyone who is new to Medical Devices, in addition to those who would like to further their working knowledge of current requirements. Areas Covered in the Webinar: Introduction to Medical Device Regulation in Europe – background Updates on the Regulations and their impact on CERs (Clinical Evaluation Reports) How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products Who Will Benefit: Quality managers Regulatory affairs Manufacturers…

The Dubai International Paediatric Neurology Congress taking place 3-6 May 2018, will shed the light on all the aspects related to this vital specialty, from diagnosis to treatment of many neurological disorders like paediatric epilepsy, neurodevelopment disorders, neuro- metabolic and genetic disorders, neuro- immunology disorders, neuromuscular disorders, and much more. This one of its kind scientific platform with elite professionals from the field of paediatric neurology, will give you the opportunity to network, build relations, and exchange knowledge. So come and join the Join the Dubai International Paediatric Neurology Congress and be a part of this exceptional congress for a…

Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…

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…

Course "Risk Management in Medical Devices Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Gaps, incorrect or incomplete implementation of software 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 device software in a regulatory compliant environment. Software risk…

Overview: Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. Areas Covered in the Session: GMP Regulations that Apply to Analytical Laboratories Reviewing Documentation Advance Preparation for the Audit Auditing Styles and Structures Who Will Benefit: External and Internal Auditors Supervisors and Analysts in Quality Control Laboratories and Quality Assurance Groups Supervisors and Analysts in Contract Testing Laboratories Speaker Profile: Steven S. Kuwahara , Ph.D. is the founder…

Training Options Duration: 60 Minutes Thursday, May 3, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar for HIPAA Covered Entities and Business Associates will identify the top OCR HIPAA enforcement priorities for 2018 and explain simply how you can master HIPAA compliance requirements for each enforcement priority. Why should you Attend: HIPAA Compliance is in crisis throughout the United States. The Office for Civil Rights (OCR), the HIPAA enforcement arm of the U. S. Department of Health and Human Services has just announced results of its recent HIPAA Compliance Audits of Covered Entities (CEs). The audited…

This webinar will provide attendees with the knowledge and skills needed to develop and produce an OTC drug product for marketing and sale in the U.S. Learning Objectives: Gain a comprehensive understanding of how OTC drug products are regulated in the U.S. Learn to distinguish between a potential Rx pharmaceutical product and an OTC drug. Recognize the difference between the various pathways for commercializing an OTC drug product. Understand how to identify and successfully navigate an OTC Drug Monograph. Recognize when reliance on a Proposed Rule, Final Rule and/or Drug Monograph is appropriate. Understand how to determine whether an Ingredient…

OVERVIEW The basic provisions of privacy for protected health information are well known in HIPAA. Exceptions abound for various law enforcement purposes as applied to both the federal and state government and its law enforcement activities, including criminal and civil matters. Erase the uncertainty and doubt that exists when the health care practitioner is confronted with a police demand for information. What can you release? To whom? Do you have to notify the patient? Should you notify the patient? What must you document as a permitted disclosure when the police call? Find out in this informative webinar that arms you…

OVERVIEW Phase 2 of the new CMS requirements were to be in place by Nov. 28, 2017. We will look at most Phase 2 requirements in detail. Let this be a moment for your team to solidly know what is required and together assess your home’s compliance. Proven culture change practices that are now part of the Phase 2 requirements and those that contribute to compliance will be highlighted. WHY SHOULD YOU ATTEND This investment in time and thinking will assist you to solidly know what regulations pertain to your work. You will not be dependent upon others to tell…