Health and Medicine

The meeting will focus on the use of echocardiography and other imaging modalities for valvular heart disease and heart failure. The basic and the state-of-the-art echo practice will be presented with lectures and breakout sessions. Focus on optimal use of 2-D, 3-D, and strain imaging in the operating room, hemodynamic as well as cardiac emergencies, the emergency department, cardiac catheterization laboratory, and other important clinical areas where echo is essential. Echo has become an essential tool for all clinicians involved in managing patients with known or suspected heart diseases. Echo is also widely used for clinical trials in assessing cardiac…

ME Conferences invites all the participants from all over the world to attend “World Congress on Nanomedicine and Nanotechnology in Healthcare” During 17-19 September, 2018 at Abu Dhabi, UAE. This includes a well-balanced line-up of speakers, covering both broad and specific topics of interest. And it provides an opportunity to learn about the complexity of the Diseases, discuss interventional procedures, look at new and advanced Nanotechnology and their efficiency and efficacy in the treatment of various diseases and also in Healthcare treatments.

19th World Obesity Congress" in Bangkok, Thailand during July 10-11, 2018, is an International Event that is an integration of the science, theory and clinical knowledge for the purpose of analyzing, interpreting and to lessen obesity-based distress or dysfunction and to promote individual health and personal development. Obesity conference 2018 mainly aims to promulgate knowledge in both life sciences and medical sciences need in course of research work and therefore would be a perfect venue of Bangkok, Thailand to share and develop knowledge on key tools. Obesity Summit 2018 is anticipating participants from 40 and more countries across the globe…

The MedTech Commercial Leaders Forum is Europes largest medical device-specific commercial event for good reason. With a unique range of stakeholders including payers and customers, fresh perspectives from industry and the leading solution providers in the MedTech commercial space, this is the only event Commercial, Sales, Marketing, Brand, Distribution & Procurement Directors need to attend. 4 Events in one: 1. MedTech: Innovative Customer-Centric Business Models 2. MedTech: Sales Force & Distributor Effectiveness 3. MedTech: Multi-Chanell & Digital Marketing 4. MedTech: Economic Value Demonstartion for MedTech

This 3-day forum is the “must attend” event for those senior decision-makers looking to drive their medical affairs teams and departments and enhance their KOL& stakeholder engagement at all levels. 4 Events in one: 1. MedAffairs: Strategy & Patient-Centricity 2. MedAffairs: Digital Medical Communications 3. MedAffairs: Real World Evidence & IITS 4. MedAffairs: MedTech

The program highlights key topics in cardiology to keep the practitioner current, with an emphasis on cases, updates, and clinical guidelines. The diagnosis, management, and prevention of common rhythm disorders, atrial fibrillation, and ventricular arrhythmias will be reviewed along with challenging aspects of congestive heart failure, coronary artery disease, valvular heart disease, and myocardial disease. Special sessions will highlight ECG pearls useful in all aspects of cardiology. There will be an emphasis on patient management, case-based presentations, and panel discussion sessions to provide interaction between the faculty and attendees. Mayo Clinic and guest faculty will share "pearls" to aid in…

This program will provide an in-depth assessment of the current status of cardiovascular disease in women, with a focus on risk assessment, diagnostic testing modalities and treatment options. The course will offer new paradigms in understanding the mechanisms of sex differences in cardiovascular disease, and provide participants with tools to translate new knowledge into sex- and gender- specific patient care. Focus areas include cardiovascular conditions that present uniquely or differently among women. Novel approaches will be presented to optimize prevention, diagnosis treatment and outcomes for conditions such as heart failure, non-obstructive coronary disease, microvascular disease, spontaneous coronary artery dissection, and…

Europe's Select TMF Event - Superior Networking and Dissemination of Successful Practices This summit continues to grow in popularity and renown among discerning TMF professionals. Pioneering and illustrious leaders of the 7th European TMF Summit constitute a high calibre speaking faculty who are eager to share their insights and experiences. The synergy of each year's cohort amplifies the compelling and meaningful content that this event is known for. The rich discourse and participatory character of the case studies, interactive workshops, panels and expository sessions ensure that you will to return to work prepared, equipped and confident your ability to realize…

In recent years the field of neurology has witnessed enormous growth in clinical and basic data. Conferences are more informative but there is often only limited time for thorough discussions. Consequently a gap appears between the expansion of knowledge and its dissemination and use. CONy provides a platform for international experts to discuss and compare experiences. The core of the CONy Congress are the debates which enable participants to discuss unresolved issues with leading world experts.The Congress aims to provide the most recent data armoring the clinician with reliable, up-to-date scientific information, helping in everyday patient care. Main topics include…

According to the FDA, CFR part 58, good laboratory practices (GLPs) are a set of guidelines for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products such as food and color additives, human and animal drugs, medical devices for human use, biological products and electronic products that are regulated by the FDA. Areas Covered in the Session : >. Understanding good laboratory practices (GLP) -GLP as an FDA regulation -Definition of GLPs -History of GLPs -Why were GLPs created? -Objectives of GLPs -Mission of GLPs >.The objective of GLPs and…

There are many different types of microbial contamination that can occur in pharmaceutical manufacturing. Some of the sources include: water, raw materials, excipients, in-process materials and samples, the manufacturing process, the product itself, and the general manufacturing environment. As such, there is no one size fits all investigation. Microbiological testing covers a wide range of products, processes and environments, therefore representative samples from each of these categories forms the basis of what gets investigated. Why You Should Attend: Medical device regulations in the US and the EU are foundational to the remainder of the regulations that are applied to medical…

Learning Management Systems (LMS) are important tools for assuring and demonstrating that pharma companies maintain their staff training, and their efforts are up-to-date. These systems often boast great functionality but also have limitations that must be overcome for companies to use them effectively. A specific area that is not well understood is the development of training curricula in LMS systems, which presents its own unique challenges and takes far more time to implement than is commonly thought. Learning Objectives: >. Articulate what constitutes a Pharma curriculum >. Distinguish a true Pharma curriculum from common misconceptions regarding Pharma curricula >. Work…

Risk Elimination. Risk Management. Risk Mitigation. This is the language of upper management, that we as auditors from any industry must learn, if we truly want to effect positive change throughout our environment. During this presentation, the various phases of the audit process will be viewed through the lens of ISO 31000 and ISO 14971. Attendees will learn how to define, recognize, and manage risk through their audit program. Case studies will be reviewed, as we discuss how to incorporate risk management thought, language and techniques into our internal audit process. Areas Covered in the Session : >. Auditing fundamentals…

“In aseptic processing, one of the most important laboratory controls is the environmental monitoring program. This program provides meaningful information on the quality of the aseptic processing environment (e.g., when a given batch is being manufactured) as well as environmental trends of ancillary clean areas. Environmental monitoring should promptly identify potential routes of contamination, allowing for implementation of corrections before product contamination occurs.” Why You Should Attend: This webinar will first explain the various US and international regulatory requirements for various clean room classifications, as well as the environmental monitoring of clean room environments. Next, the presentation details the benefits,…

This webinar provides an overview of the Quality Management System requirements. We will discuss ISO Quality Management standards and the FDA Quality System requirements. Medical device companies are utilizing ISO standards to build their business management systems because of their benefits and as a necessary step to market their products globally. Areas Covered in the Session : >. Understand the Quality Management Principles >. Discuss the benefits of an effective QMS >. Review the Quality Essentials >. Procedure Development >. Understand the required documentation: >. Quality Manual >. Policies >. Procedures >. Work Instructions Who Should Attend: >. Quality Associates…

The 27th World Congress on Diet, Nutrition and Obesity Conference 2018 going to be held at Auckland, New Zealand on the 7th and 8th of September 2018 is aimed to give an opportunity to the experts in the field of nutrition to examine the most recent progressions and difficulties in the field at the Obesity and Nutrition Meeting. Submit your research work abstract and register for the conference as a Speaker/Delegate now to avail Early Bird discounts on accommodation and registration and get published in Obesity and Nutrition Journals. To know more download the brochure for Diet Congress 2018. Blog:…

Eye 2018 is all about providing a resourceful and knowledgeable arena for the participants in the field of ocular science. We strive to provide a perfect stage to share knowledge and experiences and encourage people to carry out effective researches and works to combat against the global threat, BLINDNESS. It is all about Inspiring and get Inspired!! We have research expertise from different parts of the world coming to share their latest research works in the field of ophthalmology, optometry and vision science. To inspire the young minds we are glad to present a special category - The Young Researcher…

Human Error occurs in all settings. In the world of pharmaceutical manufacturing, the result of that error can result in loss of product or at the most extreme, injury to patients. Human is a frequent occurrance in pharmaceutical manufacturing. It occurs even when every obvious preventive actions have been employed such as effective compliance documentation development and training. Areas Covered in the Session : >. Understanding Human Error >. Nature of human error in pharmaceutical manufacturing >. Approaches to investigating Human Error >. The root causes that are directly attributable to Human Error >. The role of leadership in Human…

This training program will illustrate how these two different concepts are integrated (Phase 1, 2, and 3 vs. Stages 1, 2, and 3) and where do they merge. Attendees will learn if they exist independently of each other or do they complement each other to enhance, build and provide a product. Areas Covered in the Session : >. How these two different concepts are integrated (Phase 1, 2,and 3 vs. Stages 1, 2, and 3) >. Where do they merge? >. Do they exist independently of each other? >. Do they complement each other to enhance, build and provide a…

The Pharmaceutical and Biotech industries are going through tremendous changes that have been increased by the recent global financial challenges. The FDA is promoting the use of Quality-by-Design (QbD) as an approach for helping companies speed up development and improve their operations. In addition the FDAs new Process Validation Guidance promotes Continued Process Verification. Sampling is an essential element of both process and product development and continued process verification. Areas Covered in the Session : >. Principles for developing useful sampling plans and procedures >. When “Square Root (n)+1” is a valid sampling plan >. Creating a process sampling system…