Scope : The dissolution toolkit provides a description of best practices associated with the mechanical calibration and performance verification test for the USP basket and paddle dissolution apparatuses and test assemblies. The best practices have been developed based on experience gained by the USP laboratory (9, 13, 14, 15) and with suggestions from the USP Expert Committee on Biopharmaceutics. While not a standard requiring rigid compliance, the dissolution toolkit is intended to provide information aiding the dissolution laboratory in the effort to obtain valid dissolution testing results.
Dipl. -Ing. Hans Anthony, ST
He was born in Dabo Singkep, Riau in 1987. He completed his study by receiving his Dipl.-Ing and Bachelor of Engineering Degree in Pharmaceutical Engineering Department from Swiss German University. He was graduated with Cum-laude and his thesis is patent registered with the title 'Production of Pharmaceutical Hard Capsule Shell from Corn Starch'. He was appointed as the Managing Director of PT. Pharma Test Indonesia after finishing a complete training in Pharma Test Headquarter, Germany.
He was born in Sukabumi in 1988. He finished his study in Physical Instrumentation Department of University of Indonesia. Prior to joining PT. Pharma Test Indonesia, he has work experiences in several companies such as PT. Telkom Indonesia and PT. Airfast Indonesia. He has good personality and a hard worker. He joined PT. Pharma Test Indonesia in 2010 and has been attended the training in Pharma Test Headquarter in Germany.