Conférences - Physique appliquée: Biophysique et génie biomédical - États-Unis

Sélecionner un pays:
Allemagne (1) - Australie (1) - Bosnie-Herzégovine (1) - Canada (1) - Chine (2) - Inde (1) - Italie (3) - Liban (1) - Lituanie (1) - Pays-Bas (1) - Portugal (3) - Royaume-Uni (3) - Suède (1) - Turquie (1) - États-Unis (19) - TOUS LES PAYS (40)

1
GLP Comparison with GMP in Quality System -2017
04 oct 2017 • online, États-Unis
Résumé:
Good Laboratory Practice (GLP) is a quality system which intend for non-clinical studies and was revised by several bodies. GLP is a unique quality system in the sense it is intend for non-routine processes and activities.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Veterinary Companies, Study Directors, Laboratory Managers
Identifiant de l'évènement:
936050
2
What are Standards for Medical Device Software -2017
10 oct 2017 • online, États-Unis
Résumé:
With various changes to standards and regulations, it is important to understand the criteria for compliance, this is your DIY guide to the changes in standards, specifically covering the IEC 62304 standard.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Business Analysts, Requirements Analysts, Product Managers
Identifiant de l'évènement:
936137
3
Laboratory Have an Instrument Calibration Program -2017
10 oct 2017 • online, États-Unis
Résumé:
This web seminar builds on the terminology found in 21CFR160(b)(4) and introduces terminology and concepts not found in the regulation, but necessary for an effective calibration program, such as instrument classifications.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Laboratory Managers, Laboratory Supervisors, Laboratory Analysts, Quality Assurance Managers
Identifiant de l'évènement:
936125
4
Compliance for Computer Systems Regulated by FDA - 2017
10 oct 2017 • online, États-Unis
Résumé:
The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Analytical Chemists, Laboratory Managers, Automation Analysts
Identifiant de l'évènement:
936179
5
Medical Tubing 2017
10 oct 2017 - 10 nov 2017 • Woburn, MA, États-Unis
Résumé:
Medical Tubing 2017 will address the latest tubing and catheter developments for a wide range of medical requirements including intravenous, infusion, dialysis, respiratory, feeding, and drainage applications. It will also examine the latest standards and certification requirements in this heavily regulated sector.
Contact:
Stephanie Berchem;     Tél.: [610-478-0800];     Email.: sb@amiplastics-na.com
Identifiant de l'évènement:
851284
Sujets apparentés:
6
Cybersecurity and Computer Systems Validation - 2017
11 oct 2017 • online, États-Unis
Résumé:
Computer systems used in highly regulated companies include sensitive and valuable information. Some of this information includes valuable electronic submissions, clinical information, medical device design control records, legal information, and other such information.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Validation Engineers, Validation Project Managers, Program/Project Managers
Identifiant de l'évènement:
936167
7
Batch Record Review and Product Release - 2017
13 oct 2017 • online, États-Unis
Résumé:
A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Quality Assurance, Batch Record Reviewers, Production Personnel
Identifiant de l'évènement:
936133
8
Medical Device Engineering Change Control - 2017
17 oct 2017 • online, États-Unis
Résumé:
This webinar will describe a system, based on the regulations and practical experience that will allow for efficient control of the change process. It will be compliant but not cumbersome or overly time consuming. The difference between pre release and post release change control will be explained.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
QA/ QC Personnel, Engineering Management, Regulatory Personnel
Identifiant de l'évènement:
936121
9
Analytical Instrument Qualification and Validation Processes - 2017
17 oct 2017 • online, États-Unis
Résumé:
In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Process Owners, Quality Engineers, Quality Auditors
Identifiant de l'évènement:
936153
10
How to Develop the Risk Management File - 2017
18 oct 2017 • online, États-Unis
Résumé:
The single most important element of medical device risk management is the Risk Management Plan (RMP). It ranges from Top Management's risk policy to review and approval of the Risk Management Report. Get these items wrong and the rest of your risk management process will suffer.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Top Management, R&D Managers, Risk Managers
Identifiant de l'évènement:
936185
11
483 Covers a Broad Gradation of Problems
25 oct 2017 • online, États-Unis
Résumé:
How you respond to the 483 should provide the foundation for any future communication with the FDA about a particular inspection. Understanding how FDA organizes its evaluation of the 483 can facilitate the FDA’s review in your favor as it is well organized, succinct and provides proper documentation.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Manufacturers, FDA Consultants, Legal Counsel
Identifiant de l'évènement:
936184
12
NIST Cybersecurity Framework For Computer Systems Validation
25 oct 2017 • online, États-Unis
Résumé:
Computer systems used in highly regulated companies include sensitive and valuable information. Some of this information includes valuable electronic submissions, clinical information, medical device design control records, legal information, and other such information.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Validation Engineers, Validation Project Managers, Program/Project Managers
Identifiant de l'évènement:
936249
13
Guidance on Software and Device Changes and the 510(k)
30 oct 2017 • online, États-Unis
Résumé:
The first guidance document clarifies key terms and provides insight as to how a risk assessment can help medical device manufacturers to evaluate whether a new 510(k) is required.
Contact:
Event Manager;     Tél.: [18004479407];     Email.: support@compliance4All.com
Sujets:
Compliance Managers and Auditors, Lab Managers and Analysts, Automation Analysts
Identifiant de l'évènement:
936160
14
ANTS — 2017 IEEE Albany Nanotechnology Symposium
16 nov 2017 • Albany, NY, États-Unis
Résumé:
Conference focuses on application nanotechnology for semiconductor manufacturing, material and bio-medical device development.
Identifiant de l'évènement:
922194
15
SPMB — 2017 IEEE Signal Processing in Medicine and Biology Symposium
02 dec 2017 • Philadelphia, PA, États-Unis
Résumé:
IEEE SPMB is a single-day symposium designed to promote synergy between the healthcare industries and signal processing researchers. Featured topics include: Analysis of Biomedical Signals and Images, Machine Learning and Pattern Recognition, Signal Processing in Bioinfomatics, Time-frequency and Non-stationary Signal Analysis, Wearable Healthcare Devices, Data Mining and Analytics in Healthcare, Security and Reliability in Medical Technology and Emerging Medical Devices and Applications.
Identifiant de l'évènement:
927000
16
Cancer Imaging and Therapy
02 avr 2018 - 06 avr 2018 • Hollywood, États-Unis
Résumé:
The Cancer Imaging and Therapy conference will focus on optical methods in cancer, centered on imaging and treatment of cancer. The conference will accept submissions on topics on the molecular and cellular level, such as reporters and theranostics; on the tissue and pre-clinical (animal) level, such as pathology methods and advances in imaging of tumor models; and on human tissue and living human subjects, when specifically dealing with cancer. More generic biomedical optics and biophotonics research involving human tissues or living human subjects should be submitted to the Clinical and Translational Biophotonics conference at this congress.
Identifiant de l'évènement:
836351
Sujets apparentés:
17
Clinical and Translational Biophotonics
02 avr 2018 - 06 avr 2018 • Hollywood, États-Unis
Résumé:
The Clinical and Translational Biophotonics (CTB) conference will focus on research that has demonstrated human clinical applications, such as bioimaging or biosensing of human tissue specimens, first-to-human investigations of new optical imaging technologies for disease detection, diagnosis, or monitoring, clinical studies, and larger clinical trials. Biomedical optics and biophotonics research involving pre-clinical animal models or fundamental technology research should be submitted to other conferences at this congress.
Identifiant de l'évènement:
836350
18
ISBI 2018 — 2018 IEEE 15th International Symposium on Biomedical Imaging
04 avr 2018 - 07 avr 2018 • Washington DC, États-Unis
Résumé:
The IEEE International Symposium on Biomedical Imaging (ISBI) is the premier forum for the presentation of technological advances in theoretical and applied biomedical imaging. ISBI 2018 will be the 15th meeting in this series. The previous meetings have played a leading role in facilitating interaction between researchers in medical and biological imaging. The 2018 meeting will continue this tradition of fostering crossfertilization among different imaging communities and contributing to an integrative approach to biomedical imaging across all scales of observation.
Identifiant de l'évènement:
942017
19
IMBioC — 2018 IEEE International Microwave Biomedical Conference
14 jui 2018 - 15 jui 2018 • Philadelphia, PA, États-Unis
Résumé:
Biological and medical applications of microwaves and RF systems Radar, imaging and sensor applications Biological effects and modeling Remote monitoring and communications Wearable and implantable wireless devices and Body-centric Communications RF and millimeter-wave techniques for physiotherapy Emerging techniques and applications
Identifiant de l'évènement:
895621

États-Unis: liste de tous les évènements/conférences.



Conference-Service.com met à la disposition de ses visiteurs des listes de conférences et réunions dans le domaine scientifique. Ces listes sont publiées pour le bénéfice des personnes qui cherchent une conférence, mais aussi, bien sûr, pour celui des organisateurs. Noter que, malgré tout le soin que nous apportons à la vérification des données entrées dans nos listes, nous ne pouvons accepter de responsabilité en ce qui concerne leur exactitude ou étendue. Pensez donc à vérifier les informations présentées avec les organisateurs de la conférence ou de la réunion avant de vous engager à y participer!

Les organisateurs peuvent soumettre une réunion ou une conférence pour inclusion dans nos listes, et ceci gratuitement.

AIP Conference Proceedings
IOP Conference Series
Pre-Filled Syringes Europe

Dernière mise à jour: 03 Septembre 2017