At Envigo, our Pharma Consultancy Group is committed to supporting your key regulatory, clinical research, quality and pharmacovigilance (PV) requirements, as well as program management from pre-clinical to clinical.
Our expertise includes knowledge and experience of a range of healthcare industry sectors including pharmaceuticals, biopharmaceuticals and medical devices, and the required scientific disciplines within these industries coming from manufacturing, chemistry, toxicology, non-clinical, clinical and post-marketing.
We work with a full range of medicinal products including new chemical entities, biologics, advanced therapy products and generics. Additionally, we provide regulatory support for the development of devices, drug and device combinations, and borderline products.
Our experts are on hand to discuss your drug development programs. Please fill in the form below to request a call back.