Industries / Pharma & Life Sciences
Filtration you can take into an audit.
Filtration you can take into an audit.
Filtration you can take into an audit.
You need proof,
not promises.
You need proof,
not promises.
You need proof,
not promises.
In pharma, a filter failure can mean a failed batch or a failed inspection. You need proof, not promises.
In pharma, a filter failure can mean a failed batch or a failed inspection. You need proof, not promises.
In pharma, a filter failure can mean a failed batch or a failed inspection. You need proof, not promises.
From first stage
to terminal filtration.
From first stage
to terminal filtration.
From first stage
to terminal filtration.
Pre, Fine and Bag filters are batch tested in-house to ISO 16890. Every HEPA filter is individually tested to ISO 29463, with a test record per serial number.
Pre, Fine and Bag filters are batch tested in-house to ISO 16890. Every HEPA filter is individually tested to ISO 29463, with a test record per serial number.
Pre, Fine and Bag filters are batch tested in-house to ISO 16890. Every HEPA filter is individually tested to ISO 29463, with a test record per serial number.
Ready for validation
Ready for validation
Ready for validation
Documentation to support GMP validation and requalification.
Documentation to support GMP validation and requalification.
Documentation to support GMP validation and requalification.
Closer to your facility
Closer to your facility
Closer to your facility
Local manufacturing for faster replacements across Bharat.
Local manufacturing for faster replacements across Bharat.
Local manufacturing for faster replacements across Bharat.
Explore our testing capabilities
Explore our testing capabilities
Explore our testing capabilities
Testing and documentation support, rather than replace, facility qualification.
A complete train.
Each stage has a role.
A complete train.
Each stage has a role.
A complete train.
Each stage has a role.
A starting point for specification, subject to your facility and operating conditions.
A starting point for specification, subject to your facility and operating conditions.
A starting point for specification, subject to your facility and operating conditions.
Pre-Filters
Pre-Filters
Pre-Filters
Fine / Bag Filters
Fine / Bag Filters
Fine / Bag Filters
Terminal HEPA
Terminal HEPA
Terminal HEPA
Select around airflow, operating conditions and your current specification.
Select around airflow, operating conditions and your current specification.
For your cleanroom.
For your cleanroom.
For your cleanroom.
Need help with your requirement? Speak to our team.
Need help with your requirement? Speak to our team.
Need help with your requirement? Speak to our team.
Yes. Prysm supplies HEPA filters for pharma cleanrooms, API plants and formulation units, along with pre and fine filters for their AHUs.
Prysm HEPA filters are individually tested to ISO 29463 and supplied with documentation to support your GMP qualification and validation. Our team can also assist during audits.
Test documentation for Prysm filters is available on request, and each HEPA filter is traceable to its individual test result. Ask your Prysm contact for the reports your facility needs.
Talk to us about your facility.
Talk to us about your facility.
Talk to us about your facility.
Share your operating conditions, current specification and supply needs.
Share your operating conditions, current specification and supply needs.
Share your operating conditions, current specification and supply needs.