Konferenzen zum Thema Klinisches Datenmanagement, E-Health in den Vereinigten Staaten (USA)

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1.
 
Understanding Design Controls (to include Adaptive Designs for Clinical Studies) - By AtoZ Compliance
ID
879333
Beginn
29. Mär 2017
Ort
New Hyde Park, Vereinigte Staaten
Kontakt
AtoZ Compliance;     Tel.: [8444141400];     Email: referrals@atozcompliance.com
Themen
medical device process validation training, medical device approval process, medical device clinical studies, medical device reporting for manufacturers, medical device fmea, FDA compliance training, Adaptive Design process, Medical Device validation & verification, Medical Device Design
2.
 
Reinventing Remote Monitoring to Improve Clinical Trial Quality - By AtoZ Compliance
ID
879354
Beginn
30. Mär 2017
Ort
New Hyde Park, Vereinigte Staaten
Kontakt
AtoZ Compliance;     Tel.: [8444141400];     Email: referrals@atozcompliance.com
Themen
falsified data in clinical trials, chamberlain clinical methods, avail clinical research, clinical trial monitoring Strategies, Clinical Trial Quality, clinical trials remote monitoring
3.
 
How to get a CLIA Waiver for your Medical Device
ID
876879
Termin
20. Apr 2017 - 21. Apr 2017
Ort
San Francisco, Vereinigte Staaten
Zusammenfassung
FDA has granted precious few applications for waiver since their CLIA Waiver guidance was published on January 30, 2008. Between 2008 and 2012, FDA reviewed 34 applications for CLIA Waiver and approved 14, sometimes taking years to issue a denial. The cost of performing CLIA Waiver studies, combined with the lengthy review times and likelihood of failure, has discouraged companies from bringing new innovations to this critical public health sector.Note: Use coupon code NB5SQH8N and get 10% off on registration.
Kontakt
Referral;     Tel.: [8887172436];     Email: referral@complianceonline.com
Themen
CLIA waiver training program, fda 2008 clia waiver guidance, clia waived products labeling, ate and ler zones, clia categorization criteria
4.
 
Exploring Data Integrity To Include FDA, WHO and EMA's Latest Guidance for Industry (2015/2016)
ID
878176
Termin
18. Mai 2017 - 19. Mai 2017
Ort
Boston, Vereinigte Staaten
Zusammenfassung
Data Integrity has become a non-compliance area often observed by the FDA and reported within Form FDA 483s and Warning Letters. While various governments have observed this on a world-wide basis, the FDA has been reporting its occurrence off-shore with a greater frequency than usually observed within the United States. A lack of Data Integrity hints of a Company being outside of compliance and questions the quality of the product being produced. Note: Use coupon code NB5SQH8N and get 10% off on registration.
Kontakt
Referral;     Tel.: [8887172436];     Email: referral@complianceonline.com
Themen
Data Integrity program, cGMP compliance, regulatory requirements FDA, WHO, EMA, Data integrity workshop, data integrity issues
5.
 
ICPHM — 2017 IEEE International Conference on Prognostics and Health Management
ID
838084
Termin
19. Jun 2017 - 21. Jun 2017
Ort
Allen, TX, Vereinigte Staaten
Zusammenfassung
PHM2017 is intended for researchers, engineers and managers working in the expanding field of PHM. The primary objective is to foster collaboration and communication between academic, government, and industry PHM communities across the globe. The conference will cover a broad range of research and application topics related to PHM.
6.
 
CHASE — 2017 IEEE/ACM International Conference on Connected Health: Applications, Systems and Engineering Technologies
ID
837906
Termin
17. Jul 2017 - 19. Jul 2017
Ort
Philadelphia, PA, Vereinigte Staaten
Zusammenfassung
IEEE CHASE 2016 is an international conference in the field of connected health. It aims at bringing together researchers worldwide working in the smart and connected health area to exchange innovative ideas and develop collaborations.

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Stand vom 21. Februar 2017