Health and Medicine

Perfect for anyone who needs a formal first aid certificate or for anyone who wants to brush up their existing skills. This course is run by a fully qualified instructor and is perfect for businesses and members of the public who require formal first aid training. Each attendee will recieve a certificate that is valid for 3 years. On this course you will learn to give CPR, how to manage choking, injuries, heart attacks, diabetic emergencies and much much more. You will also learn about incident reporting and the correct way to stock and manage first aid kits. Time: 9:00…

This program will teach you to set specifications for drug substance and drug product,including use of release test data, long term stability, accelerated stability and special stability studies. The webinar will also cover changing specifications during lifecycle management. Areas Covered in the Session : >. Setting initial specifications >. How to use available data and justify specifications >. ICH specific recommendations will be discussed >. Information required to br submitted during the lifecycle >. Updating the specifications during developing and commercial phases Who Should Attend: >. Manufacturing Departments >. Supply Chain Departments >. Technical Operations Departments >. Quality Control Departments…

Conducted early in the process development cycle, the Failure Modes and Effects Analysis tool is used to identify risks and then adjust the manufacturing or service process to reduce the identified risks and improve quality. Attendees will learn practical application of Failure Mode and Effects Analysis (FMEA) as it is applied to product, process, or system design. Areas Covered in the Session : >. How to Manage designated personnel with the skills to conduct and complete an FMEA of products or processes >. Define types of FMEA’s >. The important benefits of FMEA >. Be familiar with components of FMEA…

Training Options Duration: 60 Minutes Wednesday, May 23, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: As defined by the Health Information Portability and Accountability Act (HIPAA), a Business Associate can be any organization or person working in association with or providing services to a Covered Entity who handles or discloses Protected Health Information (PHI) or Personal Health Records (PHR). With certain exceptions, a person or entity that creates, receives, maintains, or transmits PHI for a function or activity regulated by the HIPAA Privacy Rule for a Covered Entity is a Business Associate. The HITECH Act, a recent…

Overview: The plan must also include a hazard analysis, allergen analysis, factory profile, recall plan, supply chain controls, process preventive controls, sanitation preventive controls and other items. Why should you Attend: This "how to"webinar will lead you and your team through two planning options, the FDA preferred option and a more intuitive approach to planning. At the end of this webinar, your group should be able to sit down, divide up the work and get your plans finished in a couple of days. Areas Covered in the Session: FDA FSMA Preventive Control Planning Food Defense Planning Supplier Controls Allergen Analysis…

Overview: This program will teach you to set specificatons for drug substance and drug product,including use of release test data, long term stability, accelerated stability and special stability studies. Why should you Attend: Learn the recommendations of ICH for using testing and stability data to set specifications for drug substances and drug products including use of special stability studies. Learn requirements for changing specifiations through the lifestyle of the product. Areas Covered in the Session: Setting intial specifications How to use available data and justify spectifications ICH specific recommendations will be discussed Informaton required to br submitted during the lifecycle…

The 5th Annual AHA (Advanced Healthcare Analytics) Summit 2018 is returning to Boston, and bringing together again the top leaders and innovators in healthcare data, analytics and medical information for two days of insightful learning and collaborative discussion. At this dedicated forum, we will delve into how top healthcare organizations are revolutionizing the field and overcoming the challenges to leverage new and more advanced analytic capabilities to reduce cost while maximizing the quality and value of care to their patients and their community. Don't miss out on the opportunity to learn from real world case studies demonstrating how to gain…

This is your first and only opportunity to listen to the most advanced clinical case studies from Nektar Therapeutics and Amgen which explore the use of IL-2 to enhance the expansion and activation of the Treg cells. Delve deeper with expert insights from Roche and ILTOO Pharma to understand how IL-2 at low doses could selectively stimulate Treg cells. Identify yourself as a leader in this community and join the discussion exploring the challenges in translating a proof of concept in autoimmune therapies from animal models to clinic. This meeting will provide the platform for conversations to be had to…

Training Options Duration: 90 Minutes Tuesday, May 22, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: I will address specific litigated cases I have worked where the covered entity had to pay out nasty fines to the Federal government and high settlements to patients affected by inappropriate usage of the EMR system - I will also address situations where the covered entity DID NOT receive any fines or judgements (even in the event of a breach or malicious actions) due to the fact they were using the systems in a "compliant manner" I will also be addressing how…

Medical device companies face ever increasing scrutiny from the FDA and other regulators. Customers demand quality and safety. The business requires efficient and effective use of resources. Without proactive and timely metrics, a company is blind to the health of its quality system. This can lead to disaster for the company or, even worse, its customers. Areas Covered in the Session : >. How to create a balanced scorecard >. How to move from lagging to leading indicators >. How to use indices or profiles to create a more complete picture of performance >. Lack of transparency in quality/compliance data…

This event is designed for pharmaceutical, biotech and medical device professionals with responsibilities in the following areas: Product Recalls Patient Safety Product Safety Product Quality QA/QC Postmarketing Surveillance Quality Systems and Engineering Quality Compliance and Audits Complaint Handling Medical/Consumer/Regulatory/Clinical Affairs Product Complaints Compliance CMO Management Business Support Coordination Product Surveillance Clinical Operations Quality Compliance QA and Supply Integration Global Device Coordination This conference is also of interest to: Drug Safety and Complaint Software Companies Consulting Firms Law Firms Inbound Call Centers Urls; Brochure: https://go.evvnt.com/186644-1?pid=154 Booking: https://go.evvnt.com/186644-2?pid=154 Price Early Bird Pricing - Conference Only - Register by April 6, 2018: USD…

This event is designed for pharmaceutical, biotech and medical device professionals with responsibilities in the following areas: - Product Recalls - Patient Safety - Product Safety - Product Quality - QA/QC - Postmarketing Surveillance - Quality Systems and Engineering - Quality Compliance and Audits - Complaint Handling - Medical/Consumer/Regulatory/Clinical Affairs - Product Complaints - Compliance - CMO Management - Business Support Coordination - Product Surveillance - Clinical Operations - Quality Compliance - QA and Supply Integration - Global Device Coordination This conference is also of interest to: - Drug Safety and Complaint Software Companies - Consulting Firms To this: Each…

The Chronic Kidney Disease Drug Development Summit is industry’s first end-to-end drug development networking and discussion forum, dedicated to overcoming challenges drug developers face in developing chronic kidney disease therapeutics more efficacious than the current standard of care. Developed in combination with experts from Boehringer Ingelheim, Bayer, Astrazeneca, Johnson & Johnson and many more, this industry focused forum focuses on lessons learnt from CKD drug development failures, molecular understanding and reclassification towards comprehensive precisions medicine and the potential of next generation therapeutics to deliver efficacy above and beyond angiotensin converting enzyme (ACE) inhibitors and ALT1 receptor antagonists (ARBs). Be part…

As the demand for information outside of approved labeling continues to rise, the FDA has been called by the industry to provide guidance that governs off-label communications. The regulatory landscape that monitors this space is often blamed for limiting the amount of information received by patients and restricting their ability to make well-informed decisions. Given the public health issues at stake and the public interest involved, it is imperative that this event details the importance of the timely communication of truthful scientific information that currently challenges pharmaceutical, biotech, and medical device professionals. The 2018 Off-Label Regulatory Compliance Congress also explores…

During clinical trials, inspections provide a framework to ensure quality and integrity of care, data and drug performance. As sponsors of clinical trials, it is important for pharmaceutical companies to ensure GCP guidelines are upheld by implementing inspection readiness. These inspections, often conducted by the FDA, EMA, MHRA and other regulatory authorities, all have unique regulations and caveats. These nuances mean that becoming — and remaining — inspection-ready can be a difficult, time-consuming battle. Because inspections can occur without notice, sites must be prepared for visits from many different stakeholders over the course of a clinical trial. Join the 4th…

Drive innovation while navigating political and regulatory uncertainty, value-based care transitions, and financial resourcing shortages MMCC gives you the knowledge and strategies you need to • Gain regulatory clarity • Adopt alternative payment strategies • Innovate care to improve quality for your populations How? Talk freely with state officials, Association CEOs, CMS, and health plans to get candid answers to your questions • 5+Medicaid Directors from Kansas, North Carolina, Washington D.C., Maryland, and more • Network with policy makers and executive leadership from ACAP, MHPA, and more Hear outcomes from case studies and implications on the latest policies and programming…

There is an emphasis on how to reduce risk and advance drug delivery technologies for current and future needs. More specifically, we aim to cover the following: - Where is the sector going? - What are the key principles to reduce failures? - What are the unknown, unknowns? - How do we design for success and what are the guiding principles? - The conference will dedicate the afternoon of day one for a wide variety of drug delivery presentations. Partnering meetings and networking will be available throughout the meeting. To summarize what to expect at this meeting: - Addresses drug…

It gives us great pleasure to invite you to the 20th European Congress of Endocrinology (ECE 2018), on behalf of the European Society of Endocrinology (ESE), the Programme Organising Committee and the Local Organising Committee. ECE is designed to support scientific and professional interaction among all fields of endocrinology and metabolism, from bench to bedside, with the aim of advancing knowledge and improving patient care. Continuing the excitement and momentum of ECE 2017 in Lisbon, Portugal, the Programme Organising Committee has created a scientific programme featuring the best international, European and local experts as speakers in a versatile scientific programme…

Quit smoking / Quit Vaping / Quit Shisha seminar. Our highly successful quit smoking and quit vaping seminars are now in the UAE. We understand that you know all the health hazards associated with smoking. This may cause you stress, which in turn leads to you smoking more! That's why our seminars don't focus on the reasons why you shouldn't be smoking. Instead, we focus on the reasons you do smoke, and why you find it hard to quit. Our seminars have helped thousands of people quit in the UK. We keep the number of people on each seminar to…

We are pleased to announce the 30th Annual Orthopaedic Trauma Update 2018: A Tale of Two Cities, formerly known as The Columbia University NYC Trauma Course. With the addition of Dr. Paul Tornetta as Course Co-Director we will be offering a new format alternating the location each year between New York and Boston. This course is designed to present advanced instruction of upper and lower extremity trauma to practicing orthopaedic surgeons and residents. Participants will be updated on new techniques and philosophies in the modern management of orthopaedic trauma. Attendees will learn to identify and understand appropriate salvage procedures for…