The main purpose of the IIS Program to increase and stimulate external research into products, therapies and clinical management, coordinated by healthcare professionals with support from Wellspect.
The external researcher is responsible for conducting the study, i.e., acting as the study sponsor.
After submitting your proposal together with a detailed budget, the Wellspect Clinical Specialist will confirm receipt of your application for Wellspect support from the IIS program.
Within an additional six weeks your application will be reviewed by the Wellspect Clinical Research Planning Board, consisting of people with diverse expertise in Wellspect medical devices. The Board will jointly decide whether to approve, reject or ask for additional information regarding your application.If your application is approved, a written agreement between you, your Institution, and Wellspect will be established to regulate the collaboration.
We make sure to always treat an idea with respect and integrity. Your clinical research proposal is in good hands.
Are you a nurse dedicated to helping patients with problems related to the bladder or bowel? Wellspect encourages evidence related to these problems.
All our studies are conducted according to Good Clinical Practice (GDP), the Declaration of Helsinki, Wellspect HealthCare Standard Operating Procedures (SOP), applicable rules and regulations, and in compliance with the international standard ISO 14155 on clinical investigations of medical devices for human subject.
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