Harness the Power of Collaborative Partnerships
As a leading CRO in the life science industry, Toxikon has built strong partnerships with medical device manufacturers, drug makers, formulators of large and small molecules, clinical and preclinical contract research organizations.
Through these partnerships, there is a sharing of knowledge, expertise, capabilities, and a passion for answers that ultimately create a profound energy for product development. These partnerships keep our collective processes and thought-leadership at the highest levels and are always evolving, a paradigm that has developed which is a strong competitive advantage for our clients. To join this paradigm, please contact Berna Toparlar, Marketing and Communications Specialist , 781.275.3330, ext. 7172 or Berna.Toparlar@toxikon.com.
For more than 15 years, Arazy Group have utilized validation, verification and regulation processes on a diverse portfolio of medical devices. Our expertise is regulatory affairs and quality assurance for the medical device industry. We specialize in marketing safe and effective Medical Technology to international markets. Our experienced consultants are responsible for the successful registration of thousands of medical devices globally. Our customized solutions accommodate all stages of medical device’s life cycle and our adaptable services fit any application and any size organization.
The Medical Device Resource Group is a coalition of independent Twin Cities companies that collectively offer the broad expertise you need to get new medical devices to market – and support them once they've launched. Our coalition of companies offers a broad range of expertise, useful both in developing medical devices and ensuring success once launched.
Foresight Regulatory Strategies, Inc. (FRS) is a team of professionals who provide support to medical device, pharmaceutical and biologic companies for a variety of clinical, quality and regulatory activities during all phases of the product life cycle.