Conférences - Génie biomédical - États-Unis

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1
Risk Management System in Medical Devices Industry
02 avr 2020 - 03 avr 2020 • Palo Alto, États-Unis
Organisateur:
Complianceonline
Résumé:
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.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
"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
Identifiant de l'évènement:
1329173
2
Case Management Boot Camp: Strategies for Success in the Acute Care Setting and Beyond!
03 avr 2020 • New York, NY, États-Unis
Organisateur:
Complianceonline
Résumé:
Please join us for this intense one-day program that will give you the skills to succeed as a case manager or social worker in the new era of value-based reimbursement and accountable care. The world of healthcare is changing so rapidly and so is the role of case management in that world! Whether you are reading or hearing about value-based reimbursement, the Affordable Care Act, the continuum of care, bundled payments, transitions in care, or accountable care organizations, case management is at the center of it all!
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
case management boot camp, case management training, case management workshop, affordable care act, accountable care organizations (ACOs), CMS rules, utilization management, NOTICE Act, HINNs
Identifiant de l'évènement:
1329142
3
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
15 avr 2020 - 16 avr 2020 • San Francisco, CA, États-Unis
Organisateur:
Complianceonline
Résumé:
Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms and gene therapy products, as few as fifteen to twenty or as many as sixty raw materials need to be sourced before the process can be moved from initiation through completion.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
raw materials requirements, cgmp requirements for raw materials, raw material testing requirements, raw material requirements in a cgmp environment training, compendial and non-compendial testing, ICH Q9, health canada requirements
Identifiant de l'évènement:
1329244
4
5th Annual ComplianceOnline Medical Device Summit 2020
16 avr 2020 - 17 avr 2020 • Boston, États-Unis
Organisateur:
ComplianceOnline
Résumé:
Innovate novel ideas for advancements in medical device technologies without compromising their safety and effectiveness. This summit brings together some of the renowned R&D experts and technology innovators to share information regarding opportunities, obstacles, best practices and challenges in the development of the new devices. Attendees will get insight into device innovation trends and upcoming changes in the medical device regulations.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Identifiant de l'évènement:
1307138
5
Root Cause Analysis for CAPA
20 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
FDA Techniques, Root Cause Analysis, CAPA System, Online Webinar Training
Identifiant de l'évènement:
1333754
Sujets apparentés:
6
GMP Expectations for Products Used in Early Phase IND Studies
23 avr 2020 • online, États-Unis
Organisateur:
Compliance4all
Contact:
Netzealous LLC,DBA -Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Sujets:
Gmp Guidelines, FDA, Online Webinar Training, Exploratory IND studies, Quality Systems
Identifiant de l'évènement:
1333763
Sujets apparentés:
7
Equipment and Utilities Qualification
06 mai 2020 - 07 mai 2020 • San Francisco, CA, États-Unis
Organisateur:
Complianceonline
Résumé:
In this two day seminar you will learn the expectations of equipment and utilities qualification along with the development of a sound qualification program in order to develop and implement cost-effective solutions that are accepted, effective, and efficient. Through the seminar we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. Also, we will explore how your management practices of your equipment and utilities qualification programs can help or hurt on the issues that arise from non-conformance with regulators and auditors. In addition, I explain how equipment and utilities qualification must meet regulatory requirements using means such as risk management, statistical analysis and change management. This seminar presents you how to plan, perform and document qualification activities to new and existing equipment and utilities in an efficient and effective way.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
equipment and utilities qualification requirements fda, equipment qualification Master Plan, validation master plan, equipment and utilities qualification phases, maintenance of equipment and utilities
Identifiant de l'évènement:
1333794
8
SPEC 2020 — 11th International Spectroscopy Conference
17 mai 2020 - 22 mai 2020 • Monterey, Californie, États-Unis
Résumé:
SPEC 2020 is the 11th conference in the successful SPEC series, providing an occasion to both look back at the past two decades and to look forward at the next decade of translating vibrational spectroscopies into the clinic. SPEC 2020 will bring together research scientists and clinicians, from industry, academia, and medicine, to highlight and discuss recent advances in developing novel spectroscopic instrumentation and technologies to improve health and patient outcomes.
Identifiant de l'évènement:
1241089
9
Risk Management in Medical Devices Industry
04 jui 2020 - 05 jui 2020 • Boston, MA, États-Unis
Organisateur:
Complianceonline
Résumé:
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.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
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
Identifiant de l'évènement:
1333869
10
HFES 2020 International Annual Meeting — International Health Care Symposium
05 oct 2020 - 09 oct 2020 • Chicago, Illinois, États-Unis
Organisateur:
Human Factors and Ergonomics Society (HFES)
Résumé:
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.
Identifiant de l'évènement:
1226795
11
fNIRS2020 — 6th biennial meeting of the Society of functional Near-Infrared Spectroscopy
11 oct 2020 - 14 oct 2020 • Boston, Massachusetts, États-Unis
Organisateur:
Society of functional Near-Infrared Spectroscopy
Résumé:
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.
Identifiant de l'évènement:
1241084
12
FDA's Medical Device Software Regulation Strategy
19 nov 2020 - 20 nov 2020 • Boston, MA, États-Unis
Organisateur:
Complianceonline
Résumé:
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.
Contact:
Tél.: [18887172436];     Email.: referral@complianceonline.com
Sujets:
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
Identifiant de l'évènement:
1336148


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Dernière mise à jour: 27 Février 2020