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 

Sales Process of Zeptac

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. 

More features...

Ever ready for Audits

- Revisions and maintenance of standard procedures and quality procedures for cleanroom validation will be maintained ,External auditors can check it easily.  - All procedures can be shared with customers by links.

Easily Track Of Your Employees Management / Records

Manage all human resources details keep organized with address proofs , ID cards, ESIC documents , contacts , trainings and work experience and automatic sending details to customers .

Training of Employees

Planning and scheduling the periodical trainings external or internallyas per GMP quality standards to maintain consistent quality which is demands by pharmaceutical industry.

Expenses for the services can be observe for every site

For every site location, service engineer will record the travelling expense, accommodations, food expense So senior will review the all expenditures.

Complaints for Improvement

For the continuous improvement and as per the clause of ISO 17025 , organisations can record the complaints and immediately corrective can be taken.

Used Defined Formats And Reports Code Number

Organisation can change the format and report code as per customer requirement.