Cleanroom Validation

Your Reliable Partner

Be GMP compliant, take advantage of over 10 years of our experience in pharmaceutical industry

Without Measurement There Is No Control

Put your process under control with the most reliable Facility Monitoring System on the market

Thermal Validation Solutions

Choose high accurate equipment from a wide range of first class data loggers and wired systems for Thermal Validation

Precision Measurement Instruments

Measure key HVAC parameters with the unsurpassed Ventilation Test Instruments

Lab Prova | ISO/IEC 17025 ACCREDITATION

In 2009 LAB PROVA became the first regional accredited laboratory for testing that covered with accredited methods all critical parameters described by standards from ISO 14644 series (cleanrooms and associated controlled environments).

OUR SERVICES

Validation is an essential part of Good Manufacturing Practices (GMP). It is, therefore, an element of the quality assurance program associated with a particular product or process.

HVAC Commissioning and Qualification

A well designed Heating, Ventilation and Air-Conditioning (HVAC) system play an important role in ensuring the manufacture of quality pharmaceutical and microelectronic products.

Equipment Qualification

All equipment involved in critical activities, such as air handling and filtration equipment, sterilization equipment, process equipment, laboratory equipment, thermal equipment, etc. should be subject to qualification.

Compressed Air Qualification

Compressed air in most of the GMP production processes comes into direct contact with the product, and as such needs to be identified as critical utility the variability of which has an impact on the product quality and therefore should be monitored or controlled.

Thermal Mapping

Facilities, equipment, systems, vehicles and containers used to distribute, store or handle products that requires controlled temperature conditions within specified range, need to be appropriately verified in terms of their designed purpose.

Validation and Qualification Documentation

All qualification and validation activities should be planned and take the life cycle of facilities, equipment, utilities, systems, process and product into consideration.

Lab prova | OUR PARTNERS