Validation Service to Qualify Facilities, Systems and Equipment Qualification is essential to successful process validation, product quality and time-to-market. Continuum HVAC Services has an experienced team of validation professionals who provide qualification of direct impact systems and critical components in GMP environments. In addition to partnering on validation strategy, we offer a full portfolio of services including Protocol Development, Execution and cGMP, US-FDA, Schedule-M, ISO, & WHO – compliant Documentation for:
Following Documentation Preparation As Mention In Below Listed
Systems
- Air Handling Unit (AHU)
- Treated Fresh Air Unit (TFA)
- Ventilation UNIT
- Air Washer Unit
DQ, IQ,OQ
Pharma Equipment
- Dynamic Pass Box (DPB)
- Laminar Air Flow (LAF)
- Reverse Laminar Air Flow (RLAF)
- Bio Safety Cabinet
- Isolator
IOQ
Production Equipment
- DHS
- Autoclave
- FBD
- Coating M/C
- Sifter, Milling M/C
- Compression M/C (Tablet Capsule)
