Ekte LLC provides on-demand Quality, Regulatory, and Validations Engineering services and expertise to MedTech start-ups and growing enterprises. We help founders, innovators and investors in Pharmaceutical, Biological Drug, Medical Device, Human Cell/Tissue, and Dietary Supplement to commercialize and scale novel products and therapies, enter new markets, and overcome GMP, quality, and regulatory challenges. We're passionate about accelerating the progress of medical innovation and facilitating better access and better outcomes. Are you looking for help taking a new product to market, achieving cGMP compliance, or overcoming an operational challenge? Need advise from someone who's walked the path before? We'd love to be a part of your success story!