Power Your Implantable Device’s Success

Leverage ActiVie’s fractional expertise to streamline clinical trials and regulatory approvals for your implantable device.

Bringing an implantable device from concept to market is a challenging journey. From pre-clinical research to regulatory approval, ActiVie’s expert fractional clinical teams provide the targeted support you need to evaluate your product, navigate regulatory pathways, and scale your operations with confidence. We partner with you to ensure your product development meets critical milestones—quickly and efficiently.

Proven Solutions

Access a team of fractional scientists with expertise in implantable devices.
We provide everything from research design to clinical trial management, ensuring your trials are conducted efficiently and generate the robust clinical data needed for regulatory success.

Navigating regulatory pathways like FDA approval or CE Marking can be daunting. Our regulatory experts provide hands-on guidance to streamline the approval process and prepare your documentation with precision, ensuring full compliance.

ActiVie’s support grows with your company. Whether you need short-term assistance or a long-term partnership, we offer flexible solutions that evolve with your business, ensuring your product reaches market readiness faster.

Ready to accelerate your implantable device journey?
Contact us today to see how ActiVie can support your clinical and regulatory needs.

Humans First

We believe that human subjects research should always prioritize the people it serves. To develop the best products, therapies, or devices, we focus on centering human experiences and needs. We hold ourselves—and our partners—accountable to this standard, ensuring that every solution we create is human-first.