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- Bar Sealer Qualification Protocols Bundle OQ - PQ | Medical Device
Bar Sealer Qualification Protocols Bundle OQ - PQ | Medical Device
$199.00
$199.00
Unavailable
per item
Bar Sealer Operational Qualification (OQ) and Performance Qualification (PQ) Protocol Bundle product includes a Bar Sealer OQ and a PQ Protocol. Each protocol is a comprehensive 17 page document developed specifically to address regulatory requirements for qualifying medical device bar sealing equipment/process used to seal sterile medical device packaging. The Bar Sealer OQ and PQ Protocols are structured in accordance with ISO 11607 and FDA QSR Requirements.
- FDA QSR Compliant
- MDR EU 2017/745 Compliant
- ISO 11607-1/2:2019 Compliant
- ASTM F88, F1886 and 1928 Compliant
- MS Word Format
- Digital Content - Instant Download
SKU:
BAR-BUNDL
Bar Sealer Qualification Protocol Bundle
Our Bar Sealer Qualification Protocol Bundle includes an Operational Qualification (OQ) Protocol and a Performance Qualification (PQ) Protocol used to qualify process/equipment used to sterile packaging materials (i.e. Tyvek/Mylar, Foil, PA/PE, Paper/Mylar Pouches,, etc.) sealed with any make or model bar sealer.
Bar Sealer Protocol Content Overview
Each protocol specifies the manufacturing conditions, controls, testing, and required acceptance criteria. The OQ and PQ qualification protocols include the following elements:
To learn more about our Bar Sealer Operational Qualification (OQ) and Performance Qualification (PQ) Bundle contact us at [email protected]
RELATED LINKS
Tray Seal Qualification Protocols Bundle (OQ and PQ)
4 Sided Seal Qualification Protocol Bundle (OQ and PQ)
Accelerated Aging Study
Product Stability (Shelf Life) Procedure
- The manufacturing conditions, including operating parameters, process limits, and raw material inputs.
- The data to be collected and when and how it will be evaluated
- Tests to be performed and detailed acceptance criteria
- Sampling plan, number of samples and frequency of sampling for both variable and attribute data. The protocol includes a sample size justification section that notes the number of samples required to provide sufficient statistical confidence.
- Provision for addressing deviations from expected conditions and handling of nonconforming data.
- The qualification protocol includes prerequisite requirements in terms of equipment installation, personnel training and qualification, and verification of materials used in the qualification process and the review and approval of the qualification protocol by appropriate departments.
To learn more about our Bar Sealer Operational Qualification (OQ) and Performance Qualification (PQ) Bundle contact us at [email protected]
RELATED LINKS
Tray Seal Qualification Protocols Bundle (OQ and PQ)
4 Sided Seal Qualification Protocol Bundle (OQ and PQ)
Accelerated Aging Study
Product Stability (Shelf Life) Procedure
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Bar Sealer Performance Qualification PQ Protocol | Medical Device
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