Cleanroom Validation
Process & Equipment Validation
Process Optimisation
Cleanroom Validation
Start-to-Finish Cleanroom Validation Services
- Maintaining a compliant cleanroom with the required environmental conditions is quintessential for Medical Device & Pharmaceutical Manufacturers.
- We offer comprehensive validation services covering all the regulations governing your cleanroom.
- Be it a new cleanroom or an expansion of your existing cleanroom, our dedicated project team will support the execution throughout all the phases till the final handover.
Process & Equipment Validation
Comprehensive & Efficient Validation Support
- Reduce the Turn-Around-Time spent on creating the various validation documents by tapping into our team of interdisciplinary experts.
- The services we offer takes a holistic approach right from the creation of Validation Plan, URS, Risk Assessment, Protocols, Tests & Reports [IQ, OQ, PQ & PRQ], Traceability Matrix with a dedicated team for each project so that multiple projects can be managed simultaneously with ease.
Process Optimisation
Removing Your Bottlenecks
With our expert support, you can drive your projects, stay on track & be assured of an error-free completion. Our services include,
- Layout planning & optimisation (Production, Quality Control & Warehouse)
- Remediation of Risk Analysis(HIRA, RBA, FMEA), SOPs, Checklists
- Process Yield improvement & Cycle time reduction
- CAPA Handling & Complaints Management