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VALTAC – Cleanroom Validation Software for Pharma & Biotech Labs

Automate Cleanroom Validation for Accuracy & Compliance

Zeptac’s VALTAC Cleanroom Validation Software is a cloud-based solution that enables laboratories and manufacturing units to digitize cleanroom validation workflows, manage SOPs, and ensure GMP/ISO-compliant documentation.

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Automated Validation Reporting

  • Generate digital cleanroom validation reports in real-time
  • Capture environmental monitoring data such as particle counts, air pressure, and temperature
  • Eliminate manual report compilation and reduce errors

SOP & Protocol Management

  • Store and manage SOPs digitally for all cleanroom processes
  • Ensure team members follow the latest protocols consistently
  • Track SOP adherence and updates automatically

Compliance & Audit Readiness

  • Align cleanroom validation workflows with GMP, ISO 14644, and local regulatory standards
  • Maintain audit-ready digital records for regulators
  • Track deviations, corrective actions, and approvals in one platform

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Traceability & Secure Digital Records

  • Centralized storage of all validation data and reports
  • Role-based access ensures secure, tamper-proof documentation
  • Quick retrieval of historical records for audits and inspections

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.

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