Usecase 6 – Clean Rooms Pharma
Contract Manufacturing Organisations offering manufacturing capabilities to suit specific industry sectors, niche segments or perhaps simply to meet the demands of individual clients’ processes face a greater challenge when designing their facilities and cleanrooms when compared with an originator company or a single-product manufacturing facility.
The numerous clients’ varied drug substances and drug products, their constituent raw materials and APIs create a potential risk of cross-contamination, which demands that due attention and consideration is afforded to implementing satisfactory cleanroom designs, systems and procedures to address the main challenges of attaining and maintaining cleanroom conditions.
The most difficult challenges are often centred around building as much flexibility as possible into any facility and equipment investment.
Usecase possibilities
- Continuous air contamination monitoring
- Reduce Chiller failure
- Alert the service team on time
- mainten proactively
Features from SensenService
- Add Devices and manage
- Add providers and manage
- Provide permissions
- View reports in Tabular or Graphical format
- Monitor Status
- Custom Dashboard
- Business Logics
- Analytics etc
Implementation method
- Step1: Provide the parameters to be captured
- Step2: Our Team will ship you or come and install the device
- Step3: Capturing data starts
- Step4: Ready for deployment
- Step5: Will add any additional feature if needed
