Companies, API manufacturers, and finished dose pharmaceutical manufacturers. He has a solid understanding and knowledge of all aspects of the pharmaceutical business in the areas of analytical chemistry, product development, product formulation, process chemistry, CMC and FDA filing. He also has over 10 years of experience working with specialty chemical companies. Dr. Yazdi has established and managed for over 30 years several highly successful, very efficient, compliance driven, and result oriented Method Development, Method Validation, Quality Control, Stability Study program departments, and Formulation departments. He is also experienced with outsourcing projects to various organizations which operate under cGMP, FDA, DEA, ISO-9000, and EPA guidelines and regulations. Due to his vast experience, and background, he has established strong troubleshooting, and know-how skills in all aspects of pharmaceutical industries, and manufacturing facility. He joined Seqens NA / PCI Synthesis in May 2011.