Heat
1. Moist heat (steam) = saturated steam under pressure =
autoclave
2. Dry heat = oven or tunnel
Gas
1. Ethylene oxide
2. Peracetic acid
3. Vapor phase hydrogen peroxide
4. Chlorine dioxide
Radiation
1. Gamma
2. Beta
3. Ultraviolet
4. Microwave
Light
1. PureBright
Filtration
validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its pre-determined specifications and quality attributes
Subscribe to:
Post Comments (Atom)
Pharmaceutical Validation Documentation Requirements
Pharmaceutical validation is a critical process that ensures that pharmaceutical products meet the desired quality standards and are safe fo...
-
K. Dashora, D. Singh, Swarnlata Saraf and S. Saraf *. Institute of Pharmacy, Pt.RavishankarShuklaUniversity, Raipur 492 010. *Author for ...
-
Validation of the Autoclave is classified into the following 1.0 OQ – Operational Qualification 2.0 PQ – Performance Qualification The valid...
-
Cold storage is a relatively simple cold room that is commonly used to store material between 2[degrees] to 8[degrees]C. Such cold rooms a...
1 comment:
Hi,
A sterile product produced by these methods is also disclosed. The method for sterilizing is include sterilizing a selected portion of the product by exposing the selected portion to an electron beam, while shielding the remainder of the product from the radiation of the electron beam. Thanks a lot...
Instrument Sterilization
Post a Comment