Health and Medicine

Conference official website:http://www.icbbs.org/ Meeting timeJune 23-25, 2018 Meeting placeHIT Campus of University Town of Shenzhen, Shenzhen, China keynote speakers Prof. David Zhang The Hong Kong Polytechnic University Prof. Dong-Qing Wei  Shanghai Jiaotong University Published byAfter a careful reviewing process by at least 2-3 experts, accepted papers for the ICBBS 2018 will be published in International Conference Proceedings by ACM (ISBN: 978-1-4503-6409-6), which will be archived in the ACM Digital Library, and indexed by Ei Compendex and submitted to be reviewed by Scopus and Thomson Reuters Conference Proceedings Citation Index (ISI Web of Science). Paper Submission: 5-May.-2018 Call for papers: Protein structure, function and sequence…

Der Anästhesie und Intensivmedizin Refresher Aktuell findet vom 22. - 23. Juni 2018 in Köln statt. In kurzen, 30 – 40 minütigen Blöcken werden die neuesten diagnostischen und therapeutischen Leitlinien der Anästhesie und Intensivmedizin von Spezialisten präsentiert und auf Ihre Fragen eingegangen. Dabei wird vor allem auf Praxisrelevanz großen Wert gelegt. Diese praxisorientierte Fortbildung bietet in 16 Stunden: ein umfassendes Update für Anästhesisten und Intensivmediziner ein Themenreview für Assistenzärzte als Vorbereitung auf die Facharztprüfung ein Kursbuch mit den Power-Point-Präsentationen der Vorträge 16 CME-Punkte* *Für den Anästhesie und Intensivmedizin Refresher werden bei der Nordrheinischen Akademie für ärztliche Fort- und Weiterbildung 16…

Join us in Newport Beach, California at Skin Disease Education Foundation's (SDEF) 14th Annual Women's And Pediatric Dermatology Seminar(r) as we explore the chief clinical topics relevant to skin diseases in women and children. Our expert faculty present information that is immediately useful for your patients, from infants through adults. Interactive panel discussions and the opportunity to exchange ideas with colleagues and faculty, makes this unique CME/CE conference a must. This conference is for you: Dermatologists, residents, primary care physicians, physician assistants, nurse practitioners and registered nurses. Topic Highlights ACNE IN ADULTS AND KIDS ROSACEA CONTACT DERMATITIS AGING-FILLERS And TOXINS…

Middle East Infectious Diseases Conference is designed to provide healthcare professionals involved in infectious diseases with up-to-date and evidence-based clinical data to highlight key solutions to the latest challenges faced by regional HCPs. This congress will feature interactive case-studies, platform presentations, educational workshops, networking sessions, and more, to provide a comprehensive review of current issues and recent advances in selected ID topics. URLs: Tickets: https://go.evvnt.com/228189-1?pid=154 Facebook: https://go.evvnt.com/228189-3?pid=154 Twitter: https://go.evvnt.com/228189-4?pid=154 Time: 8:00 am to 5:00 pm Prices: From: USD 399.0, To: USD 2199.0

Overview: Software problems are now the third-leading cause for recalls of medical devices. Most recalls are because of incorrect verification and validation for safety. Most of the knowledge on how to do a comprehensive V&V is not widely understood. You'll come away with an actionable understanding of: Developing and creating buy-in for a project validation plan Understanding what the FDA accepts as an appropriate documentation model Beyond just in-product software V&V - understanding FDA's expectation for your testing software, ERP software and more When and how to use DQ, IQ, OQ, PQ or their equivalents How GAMP 4/5 requirements fit…

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…

Want to save your organization precious time, money, and improve quality at the same time? Implementing SPC is a great way to get this done. You will learn how…from firsthand experience and examples from companies our Expert has started, and also others where we successfully implemented SPC with enormous benefits. Although SPC has been around for several decades, its application is often erratic, sporadic, and / or lackadaisical. The result is getting a check mark for demonstrating the use of Statistical methods while getting little to no real benefit from the same. SPC can be a great tool when used…

Der Psychiatrie und Psychotherapie Refresher findet vom 21. - 23. Juni 2018 in Berlin statt. In kurzen, 30 – 40 minütigen Blöcken werden die neuesten diagnostischen und therapeutischen Leitlinien der Psychiatrie und Psychotherapie von Spezialisten präsentiert und auf Ihre Fragen eingegangen. Dabei wird vor allem auf Praxisrelevanz großen Wert gelegt. Unsere Referenten sind Experten in ihren Fachbereichen mit langjährer Erfahrung in ihrem Betätigungsfeld. Sie kommen aus renomierten Einrichtungen wie der Charité Universitätsmedizin Berlin, dem Evangelisches Krankenhaus Königin Elisabeth Herberge und der Schlosspark-Klinik Berlin. Diese praxisorientierte Fortbildung bietet in über 24 Stunden: - ein umfassendes Update für Psychiater, Psychologen und Psychotherapeuten…

Neuro Congress 2018 is an elite stage to unite overall eminent researchers in thefield of Neuroscience Brain researchers, public health professionals, scientists, academicscientists, industry researchers, scholars to exchange about state of the artresearch and technologies. The aim of this conference is to stimulate new ideasin the various fields of neurology and neurological research. From brain imaging to neural engineering, this will help in the analysis and selectthe prosthetic to help the patients. Other reasons are, gathering ofworld-class researchers and budding talent from across the globe, showcase yourresearch and get world recognition, avail chances to interact withworld-renowned scientists, perfectly designed schedule:…

The 2018 6th Annual South Spring Hip and Knee Course will bring together a highly esteemed faculty of experts in primary and revision hip and knee procedures, as well as the intricacies of today's healthcare environment. Last year's program was a great success, attracting over 150 healthcare professionals. This will be the premier orthopedic course held in the southeast in 2018. Register now and don’t miss out on this great event. We look forward to seeing you in Key Largo, FL! Time: 2:00 pm - 11:50 pm Prices: Physician: USD 795.0 Allied Health (Nurse, NP, PA, PT, PharmD): USD 300.0…

Course "Writing & Managing Effective SOPs" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Every biopharmaceutical company has SOPs, and new staff members are told that the company "has to have them" and that each employee "has to follow them". But why do there have to be SOPs and why must we follow them as written? And how can we do this effectively? Most people naturally want to do a good job. Successful managers recognize this fact and seek to channel workers' efforts in ways that will…

How does our subjective experience emerge from the brain? How does consciousness relate to the physical world? These age-old, deep questions are now at last being addressed directly and broadly by neuroscience and will become crucial in the decades to come. The spectrum of consciousness-related conundrums is rapidly expanding: we are saving islands of human brain from devastating injuries, growing cerebral organoids in a vat, and building intelligent machines that perform faster and better than any healthy subject, just to mention a few. Where does consciousness arise? Where is the boundary between insentient matter and a spark of subjectivity? Society…

This seminar will provide an exploration of eCTDs and everything that happens before and after your organization produces a regulatory agency eCTD sequence. eCTD format submission delivery mandates exist for FDA submission types. Other agencies (EU, Health Canada…) are imposing eCTD format submission mandates as well. You will gain practical knowledge of the concepts, processes and tools which are utilized to produce submission ready documents, publish technically compliant eCTD sequences, transmit/deliver eCTD sequences, manage the publishing process, support eCTD lifecycle sequences, manage multiple eCTD product dossiers, and archive your eCTDs. Learning Objectives: >. Knowledge of the CTD/eCTD and its propose…

Overview: Medical Device Recalls are an effective method of removing or correcting consumer devices that are in violation of laws administered by the Food and Drug Administration. Recall is a voluntary action that takes place because manufacturers and distributors carry out their responsibility to protect the public health and well-being from devices that present a risk of injury or gross deception or are otherwise defective. Why should you Attend: Recall of medical devices that present a hazard to consumers protects your firm from more severe action by the FDA (or other regulatory agencies). Not performing a recall correctly van lead…

Certainly the most simplistic solution to achieving compliance excellence and 483 avoidances is “to do the right things right!” But what does this really mean? I have distilled the “doing the right things right” solution into 7 separate individual keys or actions that will provide a solid foundation for the establishment of any 483 avoidance program. Why should you attend this Webinar? Because as much as we try, most regulated industries don’t have a set approach for developing a compliance program that is integrated into the fabric of their organization that is targeted to avoiding 483s, that also serves real…

Understand the requirements for investigations when dealing with pharmaceutical drug substances and products; to understand how to effectively control and conduct a laboratory investigation for unknown causes.

When an out of specification or out of trend result is obtained on an active pharmaceutical ingredient or a pharmaceutical product, both ICH and CFR guidance indicates a need for investigation. At times, the root cause is easily identified and the investigation is conducted swiftly. However, when the root cause cannot be easily accessed by initial review, it can be frustrating to determine the appropriate path for the investigation. The recent movement of bringing lean and six sigma projects into industry has had a surprising positive side effect. The tools of lean assessment of issues and problems are also excellent…

Der Allgemeinmedizin Refresher findet vom 20. - 23. Juni 2018 in Berlin statt. Mit über 5.000 teilnehmenden Ärzten zählen unsere Fortbildungen im Bereich Allgemeinmedizin und Innere Medizin zu den beliebtesten Kursen im deutschsprachigen Raum. In kurzen, 30 – 40 minütigen Blöcken werden die neuesten diagnostischen und therapeutischen Leitlinien der Allgemeinmedizin von Spezialisten präsentiert und auf Ihre Fragen eingegangen. Dabei wird vor allem auf Praxisrelevanz und Didaktik großen Wert gelegt. Unsere Referenten sind Experten in ihren Fachbereichen mit langjähriger Erfahrung in ihrem Betätigungsfeld. Sie kommen aus renommierten Einrichtungen wie der Charité, dem Universitätsklinikum Leipzig, dem Klinikum Ernst von Bergmann Potsdam oder…

Hospital care models are transforming, and nurse practitioners and physician assistants play vital roles in the care delivery of hospitalized patients. Hospital Medicine for NPs and PAs fills your CME needs. Course Highlights - 25.25 AMA PRA Category 1 Credits™ - 25.25 ANCC Contact Hours - 10.5 Hours designated pharmacology content - Pharmacology Workshop - Critical Care Breakout - Contemporary guideline-based best practices - Clinical care pathways - Diagnostic and treatment algorithms - Common clinical dilemmas - Practicing health care provider faculty Price: Registration - General Session:USD 600.0 Time: 7:00 am to 5:00 pm

Course "Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, PMAs, 510(k)s, IDEs, Post-Approval Supplements)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Why you should attend: • What do the regulations say? • Navigate the FDA drug and device approval system • Prepare, construct and submit well-written IND, NDA, BLA, PMA, 510(k) and IDE submissions and regulatory filings • Navigate the FDA review process • Identify the required regulations and guidance documents for drug and biologic submissions • Use regulations and guidance…