We help sponsors and drug developers design and execute in vitro studies that meet FDA, EMA, and Health Canada standards — from ANDA bioequivalence to reformulation and post-approval support. Our expertise ensures that IVRT/IVPT data is robust, reproducible, and submission-ready, reducing risk and accelerating regulatory timelines.

As consumer expectations shift toward evidence-based wellness products, we support nutraceutical companies in generating data to support product performance and formulation consistency. Our in vitro testing and stability services help bring transparency and scientific rigor to transdermal and dermal supplement delivery systems.

In a competitive and increasingly regulated market, we enable cosmetic brands to differentiate through science. By applying IVRT/IVPT methodologies to creams, gels, and ointments, we help clients validate skin interaction, absorption, and claim substantiation — adding value both in regulatory compliance and consumer marketing.

We act as an embedded technical partner for contract manufacturers, clinical service providers, and independent consultants. Whether you need IVRT/IVPT capabilities, protocol review, regulatory documentation, or facility-based support, Montefiore integrates seamlessly into your workflow to extend capacity, add expertise, and strengthen your client deliverables.