Can the Clearant Process® be applied to a final sealed container?
A. Yes. The Clearant Process® is designed to be applied as a final sterile barrier container pathogen inactivation step. That means doctors and their patients can be confident that no additional pathogens, or intermediate contamination were introduced into the product after being inactivated by the Clearant Process®. Materials as diverse as polyethylene, metallocized films, polyethylene terephthlate, glass, elastomer, spunbound polyolefins (e.g. such as tyvek) have been used successfully with the Clearant Process® as sterile barriers.
