Health and Medicine

OVERVIEW Discussions, presentation, and webinars regarding HIPAA regulations are usually addressed from the perspective of what the regulations entail, the necessity of compliance with the regulations, and the consequences of wilful neglect or non-compliance. This presentation addresses HIPAA regulations from a different perspective – from a personal perspective – from the perspective of the person in charge of moving an organization or facility toward full compliance with HIPAA. The by-product of this presentation will be both an understanding of, and a detailed job description for, a position mandated in the regulations – the HIPAA Security/Privacy Officer. WHY SHOULD YOU ATTEND…

This highly interactive, hands-on course features expert faculty, who will share the knowledge, principles, and skills necessary to evaluate arthroplasty patients who have pain, fracture, infection, instability, bone loss, and implant failure. You will learn how to determine an appropriate treatment course, identify potential pitfalls, and either work up and refer or perform revision surgery when indicated. You will also receive solid hands-on training in revision procedures during the cadaver labs included with your registration for the course. Prices: Physicians: USD 795.0 Allied Health: USD 400.0 Industry: USD 695.0 Residents and Fellows: USD 0.0 Residents and Fellows CME Fee: USD…

The BGS Spring meeting will cover the latest scientific research and the best clinical practice in care of older people. Our ageing population is stimulating extensive NHS service redesign to deal with the challenge of caring for larger numbers of older people both in and out of hospitals. This conference will cover core areas of interest to all specialists responsible for the health care of older people in the United Kingdom. Who should attend: - Consultants and specialist doctors in geriatric medicine - Researchers in ageing - Doctors training in related specialties - GPs wsi in Older People and GP…

Bring Clinical Research Closer to Patients & Patients Closer to Clinical Trials Arguably the greatest change we can collaborate on in bringing patients closer to clinical research is to make clinical trials a care option. Higher rates of clinical trial participation inside of a health system produces better patient outcomes, lower cost of care and happier patients. Health systems and patients get access to the latest research and pharma can get access to more patients in need of clinical research options. Clinical research is typically transactional and not integrated as part of a healthcare organization’s care options. Patients almost never…

SMi is excited to announce the latest event in their Asthma and COPD series, which returns to London on the 11th-12th April 2018. With asthma and chronic obstructive pulmonary disorder (COPD) affecting about 500 million people worldwide, opportunities in drug development are vast and reducing serious attacks by improving adherence could save $19 billion a year in U.S. healthcare costs* http://reut.rs/2xqyBjZ Recent advances in injectable biologics and smart medical devices as led to an increase in novel approaches to treating severe asthma and COPD as well as the regulations to take into consideration. As technology soars, the need for guideline…

Overview: Learn to interact with Human Resources to create a coordinated onboarding strategy, A successful onboarding strategy will combine the inputs of all these stakeholders and help create a consistent and well-understood process for the company. Why should you Attend: Onboarding in a GMP environment leads to some questions and confusion. Are contractors treated the same as long-term employees? Where does GMP Training end and HR training begin? When can employees begin working? How differently should new and transferred employees be treated in the onboarding process? This course will address the issues that accompany onboarding new or transferred employees and…

This highly immersive hands-on workshop provides the latest techniques and technology surrounding the clinical use of Extracorporeal Membrane Oxygenation (ECMO). Through integrated clinical scenarios providers will apply the knowledge gained towards the initiation and management of ECMO on simulated cases of acute respiratory and hemodynamic failure. They will deepen their understanding of the applied physiology of both venovenous and venoarterial ECMO utilizing the highest fidelity simulation labs and its interaction with conventional life support treatments. Price: Standard Registration: USD 2900.00. Time: 7:00 am to 6:00 pm.

- Medical Affairs Executive Strategy - MSL Best Practices - Research Collaboration and Investigator-Initiated Trials URLs: Brochure: https://go.evvnt.com/186030-1?pid=154 Booking: https://go.evvnt.com/186030-2?pid=154 Prices: EARLY BIRD PRICING* Register by March 2, 2018. Conference + 2 Workshops: USD 2495 EARLY BIRD PRICING* Register by March 2, 2018. Conference + 1 Workshops: USD 2195 EARLY BIRD PRICING* Register by March 2, 2018. Conference Only: USD 1895 STANDARD PRICING* Register After March 2, 2018. Conference + 2 Workshops: USD 2695 STANDARD PRICING* Register After March 2, 2018. Conference + 1 Workshops: USD 2395 STANDARD PRICING* Register After March 2, 2018. Conference Only: USD 2095 ONSITE PRICING.…

- Medical Affairs Executive Strategy - MSL Best Practices - Research Collaboration and Investigator-Initiated Trials To this: The Medical Affairs Strategic Summit (MASS) East 2018 is designed as a strategic educational platform where you are able to learn and network with 200+ life science professionals who have come together to develop a unified scientific voice and ultimately help position their medical affairs group as a strategic, customer-facing function. During this three-day summit, our esteemed speaking faculty will share valuable insights and actionable solutions through interactive workshops and plenary sessions, followed by tracked case studies, standalone presentations and panel discussions. MASS…

- 2018 Highlights - Jay Kaminski, SVP, Global Clinical RandD Operations, Celgene provides a bold and fresh approach to creating a collaborative ecosystem for a 12 month clinical trial! Dr Jeremy Chadwick, Group VP, Clinical Development Operations, Shire Pharmaceuticals, joins Dr Murray Abramson in a fireside chat to address what it takes to develop strategic relationships between sponsors and vendors that deliver results. Transformative Azmi Nabulsi, MD, Deputy Chief Medical and Scientific Officer, Head of RandD Strategic and Professional Affairs, Takeda together with Tami Klerr, EVP Global Business Development, PRA Health Sciences, talk about how their transformative collaboration is doing…

Training Options Duration: 60 Minutes Monday, April 9, 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 recent changes. He will also discuss best practices for structuring, negotiating physician employment agreements. 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 and physicians develop their employment arrangements, they must ensure the employment and compensation structures are defensible under the Stark Law. In this webinar Mr. Wolfe will describe…

Adaptive Designs in Clinical Trials, 9-10 April, 2018 With recent continuous developments in biotechnology, genomics and medicine, there is a high demand for more innovative and adaptive ways to design drug development programs.With adaptive design protocols becoming ever more complex, Adaptive Designs in Clinical Trials 2018 will equip you with the latest knowledge about the changing attitudes of the regulatory bodies to adaptive designs, how technology and experimental approaches will enrich your adaptive trials and how to ameliorate risks and errors in your adaptive designs. Adaptive Designs in Clinical Trials 2018 will continue the discussion on recent developments and applications…

Overview: The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. Why should you Attend: Today with a single audit, it is possible for a medical device manufacturer to satisfy the quality management system requirements of Australia, Brazil, Canada, Japan and the USA! This is the benefit of the Medical Device Single Audit Program, or MDSAP. However, there are some vital considerations before embarking upon this approach to satisfying the regulators of five major markets. Areas Covered in the…

Overview: This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity. Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to you, not just what it says in the regulation Avoid 483 and Warning Letters Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation Ensure data integrity, security, and protect intellectual property Who Will Benefit: IT QA QC Laboratory Staff Managers GMP, GCP, GLP Professionals Speaker Profile: David Nettleton, is an FDA…

Course "Evolution of the Quality Management System - How to go from Surviving to Thriving" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Using lecture, discussion, and exercises, this 2 day seminar will focus on taking your QMS from surviving to thriving. We'll move from understanding the regulatory requirements, how to create your QMS structure, process thinking, and developing your improvement strategy. We'll discuss tools and techniques for improvement and how to measure your progress. Why you should attend: Many companies struggle to establish and maintain a…

Course "eCTD Submissions of IND/NDA to the US FDA, EU and Canada" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good…

Product Format: Live Webinar Presenter(s): Steven T. Lawrence, MBA, JD, LLM Conference Date: Thursday, April 5, 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 Join this session with healthcare attorney Steven Lawrence, JD, MBA, LLM where he will instruct you on the current state of representations and warranties in physician practice transactions. You will learn best practices for due diligence and current trends in indemnification. Lawrence will break down standard representations and warranties in physician practice transactions and how those representations tie to both due…

ExL Events' 2nd Clinical Trial Financial Management Summit, convening on April 4–5, 2018 in Philadelphia, is designed to provide attendees with innovative solutions that deliver on-budget clinical trials using real-world data. Attendees will learn to manage contracts and negotiations with outsourcing partners and vendors; balance savings, quality, and speed in the selection of CROs and vendors; and pinpoint best practices for funding clinical trials through grants and government. Our fantastic, high level speaking faculty will tackle the all of these challenges and more during this two-day event. URLs: Brochure: https://go.evvnt.com/193735-1?pid=154 Booking: https://go.evvnt.com/193735-2?pid=154 Time: 8:00 am to 5:00 pm Prices: Early…

Training Options Duration: 60 Minutes Wednesday, April 4, 2018 | 10:00 AM PDT | 01:00 PM EDT Overview: This webinar for HIPAA Covered Entities and Business Associates will explain: What a complete HIPAA Risk Analysis - Risk Management program is and how to do one How to automate, simplify, document and complete your HIPAA Risk Analysis - Risk Management by an interactive, intuitive process: To identify and analyze Risks to all Protected Health Information (PHI) - not just Electronic Protected Health Information (EPHI) Manage Identified Risks Implement your specific, customized Risk Management Plan Archive your Risk Analysis - Risk Management-…

Challenges in Veterinary Hospital Infection Control and Antimicrobial Stewardship. Course Objectives: The objectives are to promote hospital infection control and antimicrobial stewardship in small animal practice and to educate a new generation of veterinary infectious disease specialists to be able to develop and implement infection control programmes (ICPs) and antimicrobial stewardship programmes (ASPs). Postgraduate education in this area is regarded as one of the key missions of ESGVM in order to meet the current public and animal health concerns related to the occurrence of multidrug-resistant bacteria and the increasing demand for responsible antibiotic use in veterinary medicine. The course will…