With our highly experienced and competent team, Eurofins | ams work closely with our customers as technical consultants to address many of their critical challenges, and improve/optimize their businesses.
We have supported healthcare providers, manufacturing (non-sterile and sterile operations) facilities and biotech companies. We have worked with our customers to design new microbiology laboratories and also to enhance existing ones. We have investigated and resolved operational contamination issues. We have assisted with regulatory compliance matters, including the resolution of audit observations by regulators such as the Therapeutic Goods Administration (TGA). We have also qualified microbiological and pharmacopoeia methods, and validated test methods, to name a few.
Our technical capabilities are comprehensive and we can offer the following (but not limited to) consultancy services.
- Sterile Process Validation
- Disinfectant Qualification Studies
- Cleaning and Disinfection (Sterilisation) Validation of Reusable Medical Devices
- Test Method Validation
- Contaminated Product Investigation
- Environmental Qualification and Monitoring
- Facility Audits
- Expert Witness