'Medical device' presentation slideshows

Medical device - PowerPoint PPT Presentation


Deep Brain Stimulation for Psychiatric Disorders

Deep Brain Stimulation for Psychiatric Disorders

Deep Brain Stimulation for Psychiatric Disorders. Jahdiel Franco BME 482. What is DBS?. A surgically implanted medical device called a brain pacemaker. Sends electrical impulses to the brain.

By Gideon
(454 views)

Towards ISO Standards for AD syringes: Update from WHO

Towards ISO Standards for AD syringes: Update from WHO

Towards ISO Standards for AD syringes: Update from WHO. Gerald Verollet World Health Organization 3rd SIGN Meeting - New Delhi. The Good AD Syringe definition: The World’s Perspective . Manufactured according to international standards Used only once Safe and easy to dispose. Curative

By Sophia
(313 views)

Medical Device Security Considerations – Case Study

Medical Device Security Considerations – Case Study

Medical Device Security Considerations – Case Study. Jeanie Larson Chief Information Security Officer UC Davis Medical Center @ katkarma1. Current Trends: Medical Device Security. Medical devices are easy-targets and used as entry-points into networks for attackers.

By Patman
(410 views)

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT. Objectives. Discuss the impact of FDA’s consumer protections on patient safety Describe the Medical Device Reporting Regulation as a model for patient safety

By tavon
(558 views)

Kyle J. Myers, Ph.D. Director, Division of Imaging, Diagnostics, and Software Reliability

Kyle J. Myers, Ph.D. Director, Division of Imaging, Diagnostics, and Software Reliability

FDA's role in the innovation and evaluation of evolving computer-aided diagnosis (CAD) solutions. Kyle J. Myers, Ph.D. Director, Division of Imaging, Diagnostics, and Software Reliability Office of Science and Engineering Laboratories Center for Devices and Radiological Health

By bud
(297 views)

STOP the KILLING Peter Pronovost, MD, PhD

STOP the KILLING Peter Pronovost, MD, PhD

STOP the KILLING Peter Pronovost, MD, PhD. Please answer each question with a score of 1 to 5. 1 is below average, 3 is average and 5 is above average . How smart am I How hard do I work How kind am I How tall am I How good is the quality of care we provide.

By nizana
(243 views)

Entering the North American Market

Entering the North American Market

Entering the North American Market. The Regulatory Landscape: Device Regulation in Canada Nancy Ruth Director, Medical Devices AdvaMed September 21, 2008. Authority from Food and Drug Act Health Canada - regulator Mandate: protect Health of citizens

By omar
(276 views)

Public Workshop: Quarantine Release Errors in Blood Establishments September 13, 2011 QREs Past, Present and Future

Public Workshop: Quarantine Release Errors in Blood Establishments September 13, 2011 QREs Past, Present and Future

Public Workshop: Quarantine Release Errors in Blood Establishments September 13, 2011 QREs Past, Present and Future. Sheryl A. Kochman Deputy Director Division of Blood Applications OBRR/CBER. Overview. Reason for the Workshop Definitions Past Present Future. Reason for the Workshop.

By spencer
(196 views)

Blood Establishment Computer Software (BECS)

Blood Establishment Computer Software (BECS)

Blood Establishment Computer Software (BECS). Michael Gorman, BA, MT(ASCP)SBB Consumer Safety Officer, CBER, OBRR, DBA September 15, 2009. Outline. What is a BECS? Regulations for Manufacturers Manufacturers: Medical Device 510(k) Clearance Regulations for Users Validation

By heath
(748 views)

The Impact of Regulations on Medical Device Design

The Impact of Regulations on Medical Device Design

The Impact of Regulations on Medical Device Design. Richard C. Fries, PE, CRE Manager, Corporate Reliability Engineering Baxter Healthcare Round Lake, Illinois. Extra Activities for Regulated Industries. Develop and maintain a Quality System Product Documentation Design History File

By helki
(325 views)

Towards crucial oral care of long term bed ridden elderly

Towards crucial oral care of long term bed ridden elderly

Towards crucial oral care of long term bed ridden elderly. -Need for a medical device. 4 th WHO Global Forum on Medical Devices, Vizag , India , 15 th December 2018, 14.30 PM. Dr. Steward Gracian BIRAC SIIP Fellow 2018-19 KIIT TBI, Bhubaneswar.

By pancho
(202 views)

Machine Learning Regulated by the FDA

Machine Learning Regulated by the FDA

Machine Learning Regulated by the FDA. Pilar N. Ossorio , Ph.D., JD April 5, 2019. FDA regulates medical device software.

By thais
(303 views)

Industry Adoption Roadmap Update

Industry Adoption Roadmap Update

Industry Adoption Roadmap Update. Grant Hodgkins Alcon Laboratories, Inc. Former Co-Chair, EPCglobal Industry Adoption Task Force Current Co-Chair, GS1 Healthcare AIDC Standards. Topics. IATF Roadmap Overview GS1 Healthcare Standards Overview Where We’re Going Questions and Answers.

By gavan
(266 views)

Blood borne pathogens seminar

Blood borne pathogens seminar

Blood borne pathogens seminar. Blood borne infections and tuberculosis: management of occupational exposure and isolation precautions Valerie Fletcher, M.D. Blood borne pathogens. Microorganisms that are present in human blood and can cause disease in humans.

By sarah
(168 views)

Statement of the Medical Imaging Contrast Agent Association

Statement of the Medical Imaging Contrast Agent Association

Statement of the Medical Imaging Contrast Agent Association. FDA Public Hearing on Combination Products November 25, 2002. 1. Scope of Combination Product Regulation. Concomitant use products are not necessarily combination products. Definition of combination product:

By adolph
(144 views)

Writing IEPs for Student’s with Hearing Loss

Writing IEPs for Student’s with Hearing Loss

Writing IEPs for Student’s with Hearing Loss. Carrie Spangler, Au.D., CCC-A Kirsten Marconi-Hutkay, Au.D, CCC-A Stark County ESC. IEP Defined (ODE website).

By wyatt
(1253 views)

Why Quantitative I-131 med.harvard/physics/WhyQuantitativeI-131_2

Why Quantitative I-131 med.harvard/physics/WhyQuantitativeI-131_2

Why Quantitative I-131 http://www.med.harvard.edu/physics/WhyQuantitativeI-131_2.ppt. Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical School Brigham & Women’s Hospital Dana Farber Cancer Institute The Children Hospital Boston MA. Reason. I-131. “Magic Bullet”

By kumiko
(113 views)

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT

Patient Safety and Medical Devices Sonia Swayze, RN, MA, C and Suzanne Rich, RN, MA, CT. What Makes a Good Medical Device Adverse Event Report?. Complete Device Narrative Information. Device Identifier data Device Type e.g. Infusion Pump Implantable insulin Patient controlled analgesia

By ardith
(333 views)

Human Factors Engineering: Design of Medical Devices Anthropometry and Biomechanics

Human Factors Engineering: Design of Medical Devices Anthropometry and Biomechanics

Human Factors Engineering: Design of Medical Devices Anthropometry and Biomechanics. Prof. Yasser Mostafa Kadah – www.k-space.org. Recommended Reference. ANSI/AAMI HE75: 2009. Anthropometry and Biomechanics.

By bellona
(252 views)

Rolling Out the New IEP for Psychologists

Rolling Out the New IEP for Psychologists

Rolling Out the New IEP for Psychologists. State Support Team Region 13 Sue Bitsko, Susan Burns, Gretchen Estreicher, Deb McGraw, and Patrick Wong. PR-07 IEP IEP Tools. Annotated Guide. Forms. Child’s Information. Name populates throughout the pages If 14 yrs. – Transition Pages appear

By suzuki
(128 views)

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