Micron has assembled a team of scientists and engineers with medical device, biopharmaceutical, analytical, quality, and cGMP manufacturing experience who work in state-of-the art facilities that include wet laboratory and cleanroom space. Micron works with a network of consultants and CROs to define and execute regulatory strategies, including preclinical and clinical studies.
Micron’s capabilities include:
Formulation, process, and product development
Microneedle patch and packaging design, prototyping, testing
cGMP manufacturing of clinical trial materials
Preclinical and clinical study design support
Regulatory strategy and filing
Micron develops pharmaceutical products, based on its microneedle patch technology, that are designed to provide enhanced protective (vaccine) and therapeutic (drugs) effects, superior patient compliance, and simplified administration, distribution, and storage logistics.