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Taratec is an industry-leading consultancy that provides regulatory compliance and systems lifecycle services to address the unique business and information technology challenges faced by life science companies. Our clients are the leading innovators in the pharmaceutical, biotechnology, and medical device industries. Life science companies are aggressively investing to achieve the tremendous benefits that can be derived from information technology to improve business across the drug development life cycle. While technology and automation speed time-to-market, they also present compliance challenges - challenges that must be overcome in order to satisfy all applicable regulatory laws, standards, and guidelines. Each phase of the drug life cycle has associated regulations governing technology that must be clearly interpreted and applied as guidelines and regulatory oversight change. The Life Science industry has always been focused on achieving product quality and excellence. Yet, for decades, solid profit margin objectives and regulatory control requirements have prevented most companies from achieving the "quality revolution" that swept across and transformed the automotive and semiconductor industries. Consequently, reducing waste and boosting manufacturing capabilities have become secondary to meeting regulatory and quality standards. This mode of operation is in the process of changing. As competitive pressures intensify, more Life Science companies are adopting lean principles and practices to maximize product quality, equipment reliability, plant efficiency, and throughput. Founded in 1984, Taratec is headquartered in Bridgewater, NJ with a regional operations center in Puerto Rico. Taratec currently employs approximately 200 professionals. Taratec integrates business, information technology and regulatory expertise to deliver leading-edge solutions to our life science clients.