Germfree provides controlled aseptic environments as well as primary and secondary containment to serve the rigorous demands of our clients. Our laboratory equipment, cleanrooms, cGMP facilities and biosafety labs deliver solutions across the complete life science spectrum.

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TRUBIOTECH, has been founded with a mission to help our clients find success in product commercialization and in business. We understand that great products need strong companies. Integrating business milestones and product commercialization activities is critical to overall success.We work across our industry in pharmaceuticals, medical devices, biologics, and cosmetic products.  We can support your projects large and small.  Our team of experts come to TRUBIOTECH with decades of experience in clinical development and clinical trial execution, regulatory strategy development and execution, compliance, quality assurance and audits. We have vast experience in all things GXP and love to support our clients to meet Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) at all phases of product development or in commercialized settings.TRUBIOTECH, is here so you do not have to shoulder the challenge alone.

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Clinartis is a dynamic contract research organization serving pharmaceutical, biotech and medical device companies to support Phase I - IV drug and device development. We provide a broad range of services to meet specific requirements of clinical research development programs according to the standards of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.Our broad therapeutic experience, strong project management capabilities, and core expertise in quality assurance and regulatory affairs enables us to address specific product development needs and mitigate obstacles often present in pharmaceutical and medical device development.  Clinartis is positioned to handle the most complex projects in variety of therapeutic areas covering the entire process of clinical development from study design through clinical study conduct and ultimately to regulatory submission. Organized by a group of clinical research, regulatory and quality professionals with diverse areas of expertise and experience, we offer a substantial global reach for clinical development programs, meeting the highest quality standards, and with utmost dedication to client satisfaction.

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For over 20 years, Biorasi has been to go-to CRO (Contract Research Organization) for small to midsized biopharma companies, optimizing speed-to-market solutions across global clinical trials in oncology, neurology, dermatology, and cell and gene therapy. Our #OneTeam of leaders and clinical study experts focus on the qualities necessary to succeed in today's clinical trial industry – flexibility, reliability, and transparency. It is Biorasi's mission to be a catalyst for growth, innovation, and evolution in the field of clinical research – moving the industry forward while improving results for our partners and outcomes for their patients. Our culture is based on our strong commitment to building true partnerships with our sponsors. We approach all of our trials with urgency, commitment, and resolve. Established in 2002, Biorasi is headquartered in Aventura, FL, with office-based teams around the globe. From its regional presences, Biorasi is able to directly support studies in the Americas, Europe, and APAC. We have received multiple accolades including placement in the INC 500 and 5000 list of fastest-growing companies in America, Frost and Sullivan's Entrepreneurial Company of the Year for the CRO Industry, and the CRO Leadership Award from Life Science Leader magazine.

Carol Houts

Chief Strategy Officer (CSO) at Germfree

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