About
D-TARGET is the leading expert in medical device clinical investigations and strategic regulatory services to manufacturers from all over the world. Since 1997, our global team of highly experienced professionals have helped companies both large and small to navigate the complex maze of medical device clinical research to bring their products to market. From 10-patient feasibility studies to 10,000-patient post-marketing trials, D-TARGET offers you complete and dedicated support throughout the product life cycle: • Strategic and regulatory advisory services • Clinical trial set-up and operations • Post-marketing surveillance • Registry support D-TARGET The medical device CRO ISO 9001 & 13485 certified
Technologies
DNS Made Easy
Barracuda MSP
Remote
Keywords
b2b
clinical trial design
pediatrics
agency meetings
consulting
product development strategy
clinical trial logistics
medical devices
qms setup and compliance to iso 13485
biotechnology
global compliance
cell & gene therapy
clinical research
clinical development
medical device development
data management
therapeutic expertise
risk management sop drafting
medical writing
oncology & hematology
quality assurance
safety and pharmacovigilance
data analytics
regulatory submissions (510(k)
de novo
ce marking
pma)
real-world evidence
remediation programs
neuroscience
Company Information
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Employees 5
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Founded 1997
Location
Canada
