Cleanroom Validation Management Software
The world as we know is no longer the same, and changes now occur in days and months, not for years. We always ready to give you support.
Fast Reports Generating Process
– Only reading inputs will be required
– Customizing acceptance criteria as per standards like ISO 14644 part 1,2,3, EU GMP/EC GMP, WHO TRS 961 followed by client
– After completion reports , sending links of it to customer for review process.
Ongoing Service Status Tracking
– Work flow system of software to track the details of ongoing services at every steps.
– In single vision , Senior person can reiew the whole process like allotted engineers ,allocated instruments , scope of work , work completion period, report submission status , issues pending status , Invoice generation and payment followups etc.
Build and Implement Sales Process for Cleanroom Validation Enquiries
– Creating customer profile as an enquiry
– Assigning leads automatically
– Tracking the sales process
– Understanding customer requirements
– Generating quotations with effective terms and conditions
– Time to time follow ups
– If loss the lead , recording their reasons for future perspective
Maintenance of Validation Instruments
– Up to date records of all instruments which is reviewed by external auditors.
– Schedule a periodic maintenance of instruments
– Maintenance of Traceabilities of instruments and automatic sending facility to clients.
– Calibration due notifications
Job and Validation Setup Allocation as per Availability
– Assigning the job to service engineer based on their competency and allocating the suitable instruments as per available in stock of organization.
-SMS facility with details of site location to service engineers
-Instrument movement Tracking / Traking instruments engagements at sites
Software is developed with reference of ISO 14644 and data integrity clause of GMP quality standards of Pharmaceutical industry.