IETQAN

Pharmaceutical Sector Validation & Qualification

Steam Process Validation/Qualification

Steam sterilization is the primary method used to sterilize pharmaceutical manufacturing equipment, containers, and final products. Validating this process to GMP requirements is non-negotiable for any pharmaceutical facility seeking regulatory approval.

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Dry Heat Oven Process Validation/Qualification

Dry heat ovens are used in pharmaceutical manufacturing for the sterilization and depyrogenation of glassware, instruments, and materials that cannot withstand the moisture conditions of steam sterilization.

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Depyrogenation Tunnel Process Validation/Qualification

Depyrogenation tunnels are critical equipment in parenteral pharmaceutical manufacturing, providing continuous inline sterilization and depyrogenation of glass vials and ampoules.

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Warehouse Thermal Mapping

Temperature-sensitive pharmaceutical products — including vaccines, biologics, and temperature-controlled medicines — must be stored under validated environmental conditions throughout their distribution chain.

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