Global PharmaDevice Solutions (GPDS) offers GxP compliance consulting and clinical trial management services to the pharmaceutical and medical device industries around the globe. GPDS is built with seasoned consultants, clinical trial project managers, and affiliates, including former FDA investigators with lengthy years of industry experience, both in the pharmaceutical, biotechnology, and medical device industries.
We manage both small, large, and complex GMP remediation and clinical trial projects. Our dedicated personnel strive to provide high quality services to all our clients. Due to our depth and breadth of experiences in the industry, we are well positioned in the industry to provide the expertise, skill, and training necessary to implement and improve on your GXP quality systems, quality assurance, quality control, regulatory compliance, and clinical research activities.
At GPDS we value the partnerships created when we begin a new project. The success of your business is our top priority. Most of our businesses come from repeat customers or referrals, a true source of pride and integrity. At GPDS, we understand the importance and the need to balance all your regulatory compliance and business concerns. We work diligently with you to identify and implement solutions which optimize and meet your business needs.