News

Cleanroom Validation for Hospital Seminar Topic: Cleanroom ValidationThank you for coming of Audiences from Ministry of Public Health – Design and Construction Division.

Propak Asia 2016 Thank you for visiting our booth on the Propak Asia 2016-Asia’s No.1 international processing and packaging event for Asia’s rapidly expanding food, drink, pharmaceutical and FMCG markets.

Medical Device Manufacturing Facilities and Utilities Qualification by QV Test – Total Validation for Cleanroom The manufacturing of medical devices is one of the most highly regulated sectors under FDA and ISO standards, as product safety directly affects patient health.Contamination from chemical residues or impurities can lead to severe infection or complications in end users.