Industry Events - Healthcare - Pharmaceutical

*Covid-19 Pandemic Update -- We are offering this meeting as a Virtual Webinar -- Just register online. Connection information will be provided prior to the meeting. Recordings and CME will be made available for 90 days. 10 CEU's are available to attendees. Didactic prese ..

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 ..

INTENDED AUDIENCE Practical Neuroradiology: Excellence Through Evidence and Guidelines is designed for the practicing radiologist whose work involves neuroradiology, or those involved in the neurourological sciences, neurosurgery, neurology, and/or related fields. COUR ..

Lectures and cases will cover evidence-based practice techniques and protocols for improved diagnostic accuracy in multiple applications. At the conclusion of this activity, participants should be able to: Explain the performance and processing of MRI and CT studies desig ..

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 ..

Join us at our 2nd Clinical Document World Virtual event on February 24-26, 2021, alongside your TMF, clinical quality, document management, and clinical professionals to explore a strategic clinical process and ensure a complete document management process. This interactive ..

Join us virtually to improve your medical writing strategies by understanding evolving regulatory protocols and submission guidelines, and to learn how to improve quality and content optimization. Visit our website for our frequently updated conference agenda, speaker lineup ..

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: 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 ..

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: This webinar will review the sections of the HIPAA privacy rule that under the federal emergency for COVID-19 declared in March will be under a waiver issued by the OCR and penalties will be waived. HIPAA, as a whole, is still being monitored however and the ..

Overview The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan. In this Seminar it is explained how to write the regulatory plan, and which aspects to consider. The regulatory plan describes the regulatory strate ..

Overview Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance. A ..

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan. In this Seminar it is explained how to write the regulatory plan, and which aspects to consider. The regulatory plan describes the regulatory strategy, as wel ..

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance. A strong ba ..