Scientific Process Consulting

PharmaSys combines proven experience in system compliance and validation with extensive knowledge of scientific and laboratory processes. 

We believe in proactively addressing compliance and quality control during the development phase of a scientific project, ensuring that the client has the full perspective needed to make sound scientific decisions regarding the process.  PharmaSys refers to this as “Translational Scientific Compliance”, helping the client translate their ideas and project proposals into a fully compliant product by providing validation and compliance guidance throughout the development process. 

To achieve these goals, PharmaSys has experience in GLP and validation readiness audits of preclinical, research and development laboratories, compliance of pre-clinical and clinical systems, validation of equipment and facilities for pre- and re-approval, and many other areas of compliance and validation concerns.  This background, coupled with the extensive scientific and laboratory experience of our staff, ensures quality performance for a client and their projects.

PharmaSys is also available for:

• researching a grant/scientific proposal and presenting preliminary findings and feasibility/competition studies
• designing experimental approaches to laboratory problems and concurrently ensuring the methods are compliant with federal regulations
• legal scientific consulting, including preparing case documents and expertly instructing in scientific and technical matters
• many additional scientific applications