1. Implementing, planning, designing and constructing of cleanroom and supplying and installing cleanroom fittings and equipment.

2. Involves the planning and designing of the cleanroom’s layout

3. On site project management

4. Fitting of cleanroom and installation of life science or operation equipment to be used in the cleanroom.

5. SGLMS – Upon completing construction of the cleanroom, we install the SGLMS to monitor, control, analyze and record critical indoor air quality and equipment data.

6. Testing and validation (SGQMS) – The final process before handing over the cleanroom to our customers is to perform preliminary testing, inspection and validation of the cleanroom prior to its commissioning.


Type of Cleanroom Facilities

Ministry of Health (MOH) National Pharmaceutical Regulatory Agency (NPRA) Cell Gene Therapy Products (CGTP) Pharmaceutical Inspection Co-operation Scheme (PIC/s) Current Good Manufacturing Practice (cGMP) regulated Facilities for Mesenchymal Stem Cells, Natural killer cells, T-Cell production

Ministry of Health (MOH) National Pharmaceutical Regulatory Agency (NPRA) (HACCP) Current Good Manufacturing Practice (cGMP) regulated Facilities for Food Production Plant

Ministry of Health (MOH) Cawangan Kawalan Amalan Perubatan Swasta (CKAPS) The Reproductive Technology Accreditation Committee (RTEC) Assisted Reproductive Technology (ART) In-vitro Fertilization (IVF) Ambulatory Care Center (ACC) and Operation Theatre (OT) Complex

Ministry of Health (MOH) National Pharmaceutical Regulatory Agency (NPRA) Pharmaceutical Inspection Co-operation Scheme (PIC/s) Current Good Manufacturing Practice (cGMP) regulated Facilities for drugs, vaccine, vitamins production