Dr. Kindt is a drug safety expert, specializing in IND and CIB preparation, regulatory interactions, drug development strategy design, toxicity problem solving, and the design, management, interpretation, and documentation of non-clinical safety studies.
Experience
Dr. Kindt has 19 years of drug development experience in the pharmaceutical industry, specializing in small molecule drugs in all phases of development and has been a drug development consultant for 2 years.
