PHARMACEUTICALS & BIOTECH PRODUCTS
NOTOX provides its customers with quality information regarding the non-clinical safety profile of their drug candidates. Regulatory authorities define the basic requirements for these types of research studies (i.e. toxicology, safety pharmacology, ADME or environmental toxicology). We add value by leveraging over 25 years of experience in conducting these types of studies in a contract research business setting.
Experienced and dedicated scientists work together with yours to create the optimal study design for your compound. With a thorough understanding of your business requirements, we will advance your candidates through the various development stages towards the patients.
NOTOX also provides regulatory affairs consultancy and project management to advance your product towards the market place. They are skilled in communications and able to deliver relevant information to you with full transparency and crystal clear.
Please click on the links below for more information or contact us directly.
Toxicology
