Healthcare Industry - Medical - Pharmaceutical - Biotech

19 AMA PRA Category 1 Credits™ 19 Cognate Credits World Class CME is again proud to host the annual Fetal and Women's Imaging conference in Seattle, Washington. We welcome everyone to The Westin Seattle for yet another excellent three day course in 2021. ACOG has ap ..

MISSION: To provide the highest quality continuing medical education experience to all clinicians who care for patients with chronic wounds and from this, improve patient outcomes by maintaining constant focus on the most modern and effective management techniques. - A f ..

Lectures and cases will cover evidence-based practice techniques and protocols for improved diagnostic accuracy in multiple applications in Chest and Abdominal. URL: Website: https://go.evvnt.com/683550-0?pid=2874 Prices: Practicing Physician/Industry: USD 1295.0, M ..

This course is designed to provide the tools for participants to enhance interpretation skills utilizing the latest imaging technologies. Lectures and cases will cover evidence-based practice techniques and protocols for improved diagnostic accuracy in multiple applicatio ..

Co-Chairs and Keynotes Include: - Dr Ann Daugherty, Genentech, Co-Chair - Dr James Cunningham, Allergan, Co-Chair - Dr Jeffrey Hubbell, University of Chicago, Keynote - Dr Robert Thorne, Denali Therapeutics, Keynote - Dr Kevin Healy, UC Berkeley, Keynote - Dr Sarah Hym ..

This 20th annual interdisciplinary conference offers a unique update for primary care and subspecialty health care professionals and others who care for children, youth, and adults with developmental disabilities and complex health care needs. This year's conference will be ..

We extend a warm welcome to distinguished Pediatrics Nobel Laureates, Speakers, Delegates, Exhibitors, Researchers, Students around the world to explore the Knowledge in Pediatrics and its line. We welcome all the interested members to participate in our conferences as Keyn ..

Overview: This webinar explains the inter-connected Breach Notification Rule requirements of Covered Entities and Business Associates when a Business Associate or Subcontractor Business Associate suffers a Breach. And it covers the special, more restrictive compliance req ..

Overview: This webinar will provide you with the regulatory framework and recommended guidelines, risk assessment for biological materials, structure of a robust biosafety program and on how to train employees exposed to biological hazards. Why you should Attend: This we ..

Overview: Recent cases and/or enforcement actions involving the Federal Civil False Claims Act (FCA) as well as the Medicare-Medicaid Anti-Kickback Statute (AKS) and/or Federal Physician Self Referral Law (Stark II) raise serious concerns regarding compliance issues with ..

Overview: Advancements in technology have forced organizations to rethink business models. Once controlled and orderly, these organizations are now more chaotic and complex, serving patients and customers that are better informed and with higher expectations than ever befor ..

Overview: While the universal language defined by the PMI does not always translate to the jargon regularly used by healthcare professionals, the majority of work performed by most healthcare professionals includes, or is completed defined by, project-specific work. By ..

Overview: Standard Operating Procedures (SOPs) are a regulatory requirement for industries that are governed by the FDA and other world health authorities. Currently, there is no guidance on how to develop or manage the SOP creation or the SOP quality system. Why you ..

Overview: Deviation investigations are a very common topic to be reviewed during FDA investigations. Ensuring the firm has robust and complete write-ups of these situations is key to a successful audit. Having inadequate investigations could potentially cause some severe ..

The European Medicines Agency's (EMA) Guideline on good pharmacovigilance practices (GVP), Module IV requires that risk-based audits of the quality system be performed at regular intervals to assure that it complies with the established quality requirements and to determine ..

Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part of the regulators that demands, in turn, that industry be keenly aware of the legal and regulatory duties, as well as key recent trends in e ..

This webinar will detail a data integrity governance program and principles for defining quality and data integrity into processes and systems. It will cover the common problems from FDA 483 observations and warning letters and teach you how to avoid them. ..

This course will cover validation essentials for medical device manufacturers. Attendees will learn about what processes needed to be validated and what steps you need to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and ch ..

This webinar will review not only the Anti-Kickback Statute and its safe harbors, but will provide an in-depth overview of OIG guidance and advisory opinions dealing with marketing activities, as well as a review of case law regarding marketing behavior. ..

In this care coordination training you will learn how to apply the key strategies for reducing your hospital’s cost and length of stay. Also you will learn how to appreciate the role of interdisciplinary care rounds by identifying your hospital’s strength and weakness relate ..