Personal Information
Entreprise/Lieu de travail
Ankara, Turkey Turkey
Profession
Quality Manager
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
www.elmed-as.com
À propos
I started working as the Quality Manager and Management Representative at Elmed Medical Systems. I have served as CQO since then.
Mots-clés
ra-rirs
elmed
urology
avi̇cenna roboflex
medical devices
furlas
robot
strategic planning
data
guide
development
design thinking
market report
usability
social media
eu mdr
risk management
stonemanagementtreatment
pcnl
vibrolith
#kidneystones
laser lithotripsy
ureteroscopy
eswl
stone management treatment
lithotripsy
racimatrisi
organizasyon
kys
endostone
medicalroboticsolutions
uromedya
nht
flexible urs
Tout plus
- Présentations
- Documents
- Infographies
1108 ted risk_assessment_methodology_guidance
mohammad amin saleh ahmadi
•
il y a 8 ans
TGA webinar presentation: Regulation of software, including software as a medical device
TGA Australia
•
il y a 5 ans
Webinar: "The future of European Medical Device Regulations"
pi
•
il y a 7 ans
Unique Device Identification: Manufacturer, Hospital and Global Implications
April Bright
•
il y a 5 ans
Medical Devices
Indegene
•
il y a 1 an
CER - PMS - PMCF
Katarzyna Zofia Chrusciel
•
il y a 5 ans
Clinical Evaluation in the EU for Medical Devices: Understanding the Changes in MEDDEV 2.7.1 Rev 4 and Their Impact
Greenlight Guru
•
il y a 7 ans
How to Make Postmarket Surveillance More Cost Effective
April Bright
•
il y a 7 ans
History of medical devices
SanthiNori1
•
il y a 10 mois
IMPACT OF REGULATIONS ON MEDICAL DEVICES IN CONTEXT OF INNOVATIONS
JAYA PRAKASH VELUCHURI
•
il y a 4 ans
mHealth Israel_The New Regulatory Challenges in Europe The Clinical Evaluation of Your Devices_Michael imhoff
Levi Shapiro
•
il y a 5 ans
EU MDR Preparation: Seize the Market Opportunity and Avoid the Bottleneck
April Bright
•
il y a 5 ans
New European Medical Device Regulations: Keeping Your Orthopaedic and Spine Products on the Market - OMTEC 2017
April Bright
•
il y a 6 ans
Advamed MDR IVDR update
Erik Vollebregt
•
il y a 8 ans
Legal issues relating to clinical investigation with medical devices
Erik Vollebregt
•
il y a 6 ans
Understanding how the eu clinical trials directive could have a feedback impact on the revision of the mdd dublin 2013
Erik Vollebregt
•
il y a 11 ans
Post-Market Clinical Follow Up Studies Under EU MDR and IVDR
EMMAIntl
•
il y a 3 ans
Adverse Event reporting in Medical Device Clinical Trials under the MDR
Annet Visscher
•
il y a 9 mois
Patient engagement in medical device studies
COUCH Health
•
il y a 3 ans
Europe CE Marking for medical devices under new MDR
EMERGO
•
il y a 7 ans