In the highly regulated pharmaceutical industry, whether in a general, R&D, production or QC facility, there is an intense focus on laboratory efficiency and productivity and, simultaneously, there are demanding GLP / GMP requirements to meet.
This free practical guide discusses how optimum efficiency and productivity of a typical pharma workflow can be achieved, by identifying and eliminating any particular inefficiencies, and introducing standardized processes.
This guide focuses on 5 typical applications & workflows in the pharma industry, where weighing plays an integral role: Capsule filling, preparation of culture media, sample preparation for titrator, preparation of reference standards and solutions as well as sample preparation for quantitative elemental analysis in research labs. For each of these workflows the challenges and potential process improvements are being discussed. For many typically occurring issues in pharmaceutical workflows, automation is the solution, helping to streamline procedures and eliminate the potential for manual errors, and ensuring regulatory compliance is maintained.