Faculty: Joy McElroy
One of the most useful analytical methods for cleaning validation studies is Total Organic Carbon (TOC). This includes the design, qualification and routine monitoring of the manufacturing process. While there does exist some confusion within the industry and regulatory bodies about the use of this analytical technique, it is widely used because of its assured benefits. This webinar will cover the basis of TOC as an analytical technique, including the several technologies currently being utilized. The precautions in sampling and analyses will be discussed, including the appropriate use of blank and controls.
Why You Should Attend:
TOC (total organic carbon) analysis is a nonspecific method typically being utilized to identify the presence of organic residues on cleaned product contact surfaces. TOC analysis is fast becoming the preferred analytical method of choice for cleaning validation. A number of pharmaceutical companies are developing cleaning validation methods based on a whole-product approach: a determination is made as to whether any residue is present without regard to its origin (including products, cleaning detergents, chemicals, solvents, by-products, degradants, and microbial contaminants). This method works well with TOC analysis, which can detect any API or cleaning agent residue that contains carbon in its molecular structure.
This webinar on Total Organic Carbon (TOC) will demonstrate its feasibility, method validation and transfer from the laboratory to the manufacturing floor. We will also be reviewing the feasibility study of multiple, difficult to oxidize or low solubility organic compounds.
Areas Covered in the Session :
Who Should Attend:
Attendance will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory personnel, as well as, beginning or seasoned operational personnel who will eventually participate in such efforts, will find this course particularly useful. This includes Analytical Method Development, Quality Control, and Quality Assurance personnel.
Individuals in management who interact with the above or communicate with regulatory agency inspectors to rationalize or defend cleaning validation programs will also benefit from attending this course.