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 EasyBarracuda MSPRemote
Keywords
b2bclinical trial designpediatricsagency meetingsconsultingproduct development strategyclinical trial logisticsmedical devicesqms setup and compliance to iso 13485biotechnologyglobal compliancecell & gene therapyclinical researchclinical developmentmedical device developmentdata managementtherapeutic expertiserisk management sop draftingmedical writingoncology & hematologyquality assurancesafety and pharmacovigilancedata analyticsregulatory submissions (510(k)de novoce markingpma)real-world evidenceremediation programsneuroscience
Company Information
- Employees5
- Founded1997
Location
Canada
