Medford Pharmaceuticals is committed to manufacture and supply quality pharmaceuticals thereby improving lives of patient’s. This objective is achieved by following Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in each and every stage of manufacturing process and properly monitoring them. We have a highly equipped Quality Control (QC) department with a core team of experienced professionals who will be involved in Analysis of Excipients, Intermediates, Active Pharmaceutical Ingredients (API), Finished Products, and Packaging materials. Thus, we ensure that our products are Pure, Safe and Effective which are manufactured as per methods and operating procedures as per International Standards.