Drug Development Solutions

At NUVISAN, we understand the importance of bringing new drugs to market in a timely and efficient manner. Whether you need support with preclinical studies, bioanalytical testing, formulation and chemical development, or clinical development, our experienced scientists and technicians can provide you with the expertise you need to ensure that your drug development program is successful.

Drug Development

Once a lead compound has been identified through the drug discovery process, the candidate enters the preclinical stage where its safety and efficiency are thoroughly assessed.

To support your go-no go decisions with insightful analysis and data of your drug ADME properties, a wide range of drug metabolism and pharmacokinetics (DMPK) studies can be run by our team. These studies are fulfilled by our experts in Bioanalysis, checking accurate dosage levels and measuring drug and metabolites concentration levels in biological matrices.

In parallel, the chemical properties of the drug candidate, such as solubility or stability also influence its in vivo performances. An efficient Chemical Development route design as well as Formulation Development are also key to ensure the efficacy of the drug candidate.

To maintain the quality of your drug from lab to shelf, our Analytical Development & QC team has extensive experience in designing reliable and robust analytical test methods. While moving from bench to bedside, our Clinical Trial Supply experts can support the manufacturing of your medicinal products for use in Phase I-IV clinical studies as well as compassionate use /expanded access programs. These steps are diligently run by our team to minimize risks in humans during clinical development.

To ensure the success of your Clinical Development program, NUVISAN offers a comprehensive range of services including regulatory affairs and submissions, clinical data management and statistics, medical monitoring and safety reporting, patient recruitment and retention strategies, quality assurance and auditing, project management and outsourcing solutions, and post-approval support and commercialization planning, all in addition to study design, protocol development, and clinical trial management.