Konferenzen zum Thema Medizintechnik in den Vereinigten Staaten (USA)

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1
Risk Management in Medical Devices Industry
04. Jun 2020 - 05. Jun 2020 • Boston, MA, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
Risk management is a mandatory and necessary process during the entire device life. Not only will it help to design and maintain devices efficiently, but it also ensures that the device will be as safe as possible and prevents harms to patients, users, and the environment. Like any process that tries to produce repeatable and consistent results, the risk management process must be clearly understood, including the strengths but also the limitations.By attending this seminar you will learn the main elements of ISO 14971, ISO 13485, IEC62304, IEC62366-1/-2, risk management life cycle steps and benefits, and FDA software reviewers' guidance.
Kontakt:
Tel.: [18887172436];     Email: referral@complianceonline.com
Themen:
medical device risk management training, ISO 14971 workshop, ISO 13485, quality system integration, IEC62304, IEC62366-1/-2, risk management life cycle, FDA software reviewers' guidance, SOP framework, risk rating methods, european special requirements, risk management report
Eintrags-ID:
1333836
2
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
18. Jun 2020 - 19. Jun 2020 • Virtual Training Through WebEx, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
FDA inspects many different kinds of firms. If the FDA regulates your product, they can show up at your lobby and say, “I am here to conduct an inspection.” What do you do? What have you done to prepare for an inspection? How do you deal with the investigator, including their personality? The scary part is having to explain the error of your ways to the FDA and above all, managing an administrative action, e.g., Warning Letter or Import Alert, or a legal action, e.g., civil money penalties, seizure, injunction or prosecution. This course will help you need to know and what you should do to survive an FDA inspection with the least possible pain.
Kontakt:
Tel.: [8887172436];     Email: referral@complianceonline.com
Themen:
FDA inspection seminar, FDA inspection, FDA 483, FDA warning letter, FDA investigator, FDA law, Regulatory Sanctions used by FDA, Prohibited Acts, Management Responsibility from FDA’s view, FDA Inspection Team, FDA Inspection SOP, FDA Meeting, FDA inspection Scribes, Warning Letter Responses, import alerts, inspection documentation
Eintrags-ID:
1353034
3
ISG TechXchange: Healthcare & Life Sciences
26. Jun 2020 • Virtual, Vereinigte Staaten
Veranstalter:
ISG
Zusammenfassung:
The Healthcare and Life Science Industries have long survived on steadfast business models. Bound by a duty of care, resolute governance models, and risk mitigation efforts, there has been little incentive to change – until now. A new era, generated by a more educated and empowered patient, accessibility through digital advancements, and the emergence of innovative technologies have changed these ecosystems forever. Now fast-paced and competitive, healthcare and life science organizations are in a race to remain relevant. Do you have what it takes to deliver the care, and tools, that your patients expect? Join us at TechXchange: Healthcare & Life Sciences to unearth what it takes to deliver improved health outcomes and win patient loyalty in the age of convenience and choice.
Themen:
Healthcare, Life Sciences, ISG, Technology
Eintrags-ID:
1352309
Verwandte Fachgebiete:
4
RISE Nashville 2020 — 14th Annual RISE Nashville Summit
29. Jun 2020 - 30. Jun 2020 • Nashville - virtual, Vereinigte Staaten
Veranstalter:
Arcadia
Zusammenfassung:
RISE Nashville 2020 will be held virtually on June 29th and 30th, with workshops on June 26th. This year's topic of discussion is breaking down barriers between providers and health plans.
Themen:
healthcare, health, healthcare technology
Eintrags-ID:
1357923
Verwandte Fachgebiete:
5
A Comprehensive View of FDA Regulations for Medical Devices
16. Jul 2020 - 17. Jul 2020 • Tampa, FL, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
Don’t let a common misunderstanding get you into trouble! There is more to the US Medical Device Regulations than Part 820.
Kontakt:
Tel.: [8887172436];     Email: referral@complianceonline.com
Themen:
US medical device regulations, FDA medical device compliance best practices, FDA QSR, medical device reports (MDR), Unique Device Identification (UDI), Quality System Inspection Technique (QSIT), FDA inspections, medical device manufacturer, form 483s, warning letters, Part 820, quality management system, quality assurance and quality control, device marketing requirements, CAPA, device design requirements
Eintrags-ID:
1353073
6
HFES 2020 International Annual Meeting — International Health Care Symposium
05. Okt 2020 - 09. Okt 2020 • Chicago, Illinois, Vereinigte Staaten
Veranstalter:
Human Factors and Ergonomics Society (HFES)
Zusammenfassung:
HFES events offer unparalleled opportunites to immerse yourself in new discoveries and breakthroughs in the field of human factors/ergonomics and benefit from opportunities to partner with colleagues from around the world. Come to the next Annual Meeting or Health-Care Symposium to explore, network, and participate in programs presented by a community of distinguished professionals working in diverse areas of the HF/E field.
Eintrags-ID:
1226795
7
fNIRS2020 — 6th biennial meeting of the Society of functional Near-Infrared Spectroscopy
11. Okt 2020 - 14. Okt 2020 • Boston, Massachusetts, Vereinigte Staaten
Veranstalter:
Society of functional Near-Infrared Spectroscopy
Zusammenfassung:
The meeting will span the topics of hardware development, data analysis and algorithms, computational neuroscience and neuroscience applications, clinical applications, neonatal, pediatric applications and neurodevelopment neuroscience, cognitive and social neuroscience, and global fNIRS.
Eintrags-ID:
1241128
Verwandte Fachgebiete:
8
FDA's Medical Device Software Regulation Strategy
19. Nov 2020 - 20. Nov 2020 • Boston, MA, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
medical device trade and healthcare professionals remain plagued by other issues, such as the interoperability of devices from different manufacturers, or software validation that is limited to the immediate use of the software rather than its performance with other software programs, and software hacking protection applications. In case of software malfunction, fixing the malfunction or bug can get more difficult as software gets increasingly sophisticated, customized by users and placed in a network system. Under these circumstances, it is difficult to decide who is responsible for managing and fixing software problems.
Kontakt:
Tel.: [18887172436];     Email: referral@complianceonline.com
Themen:
Seminar by Ex-FDA Official, Regulatory profile for software products, FDA mobile apps regulation, medical device software functionality, FDA and NIST software guidance, proprietary software, FDA medical device recalls, warning letters, risk management
Eintrags-ID:
1336082
9
SPIE BiOS21 — SPIE Biomedical Optics - BiOS
23. Jan 2021 - 24. Jan 2021 • San Francisco/CA, Vereinigte Staaten
Veranstalter:
SPIE - The international society for optics and photonics
Zusammenfassung:
BiOS 2021, part of SPIE Photonics West 2021, is the world’s largest biomedical optics and biophotonics conference. Topics range from biomedical optics, photonic diagnostic and therapeutic tools and systems, nano/biophotonics, new imaging modalities, OCT, neurophotonics, optogenetics, and tissue optics.

Kontakt:
Customer Services;     Tel.: [360 676 3290];     Email: customerservice@spie.org
Themen:
neurosurgery, neurophotonics, biomedical optics, biomedical imaging, SPIE, photonics west, photonic west
Eintrags-ID:
1352433
Verwandte Fachgebiete:


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Stand vom 25. Mai 2020