Quality & Compliance

NGT BioPharma Consultants’ Quality & Compliance strategic and operational consulting services span all phases of drug development for both small molecules and biologics (Mabs, duobodies, proteins, cell therapy, gene therapy, and other new modalities), beginning at the preclinical stage while extending through commercialization and life-cycle management.


Our Quality & Compliance consultants work seamlessly with other functional areas, such as Nonclinical, Clinical, CMC, and Regulatory, to provide services that include, but are not limited to, the services highlighted below:

NGT’s Quality & Compliance consultants are experienced professionals in all phases of drug development, including preclinical, clinical, registration, commercialization, and life cycle management, and cover a wide range of modalities.


For more information
please contact:

Ronay LeBlanc

860.333.9023 ext. 404

OR Contact:

Rachel Franckowiak

Senior Director, Administration