For more than 20 years, we’ve helped dozens of businesses in the highly-regulated GMP (good manufacturing practice) environment of drug development and testing. Our team of scientists is responsible for the development and refinement of new products. We provide ongoing testing for your drugs in ICH conditions and make sure that they meet all standards and parameters established by their stability date.
Integrity, communication, and sound science — these core values drive us in our research and ensure that we always do right by you (and ourselves). When you work with PD Partners, you can ensure you’ll get the best quality results. We focus on all of the details that often trip up businesses in the new product development process and provide guidance to help navigate them. From planning and formulation to testing and filing, we’ve got you covered.
Located in Tampa, Florida, our facility has 15,000 square feet of space with an adjacent unit of another 15,000 square feet. Our pristine production site has received all applicable environmental, health, and safety inspections as well as regulatory inspections to ensure it’s properly suited for your needs. We offer a full range of USP/BP/EP testing, ICH stability programs, product development, and regulatory consulting services to eliminate hiccups in the product development process.