Pharma Engineering ApS

• Validate laboratory and production equipments. From standalone units to whole packaging lines; both simple and highly computerizes systems. Outline Golden ~ Light Qualification • Authoring and reviewing qualification documents and deviation investigations Assists with expert knowledge of protein analysis including cost benefit calculations, prior to establishing an analytical program. Estimates time and costs of new equipment, personnel education, and transfer of analytical methods under strict GMP regulation. Assists transference and translate R’n’D’s downstream purification methodology to the final production record for filing with the authorities.