Supported by state-of-the-art technical facilities and a specialised international team of dedicated engineers and scientists, Parker domnick hunter is committed to supporting your validation process.
Developing partnerships
We work with you to establish the most effective filtration solution for your process based on your goals and desired process improvements including;
- Minimising product loss
- Reducing downtime
- Increased yields
- Reduce over processing
- Guarantee sterility
- Minimising risk to your process
- Extending service time
- Promoting best practice
Once the correct filters have been chosen, Parker domnick hunter work closely with you to qualify the use of our products within your process.
Development of an application specific strategy
Our Technical Group use your identified parameters to determine the whole qualification package required. This demonstrates that our filters are capable of meeting the performance goals required of your process.
By following simple step by step guidelines outlined by PDA Technical Report No. 26 (Sterilising Filtration of Liquids), we can eliminate any disruption to your business whilst achieving your long term process improvements.
Test work is carried out by our experienced team of scientists and engineers at our excellent test facilities where we are committed to conducting qualification test work on your behalf.
Meeting the standards
Global investment programmes have created first class R&D, manufacturing and support facilities across the world. We are committed to industry standards including:
- ISO 9001:2000 - Quality Management Systems
- ISO 13485:2003 - Quality Management Standards for medical devices
- PS 9100:2002 - Pharmaceutical Excipients
- ISO 14001:2004 - Environmental Management
