FAQs
Answers to common questions about our services, capabilities, and working with Panomics Biosciences.
1
What sectors do you serve?
We provide services to organisations operating across life sciences, biotechnology, pharmaceutical, agricultural, veterinary, and research sectors — both within Australia and internationally.
2
Can you develop a custom assay from scratch?
Yes. Our scientists work closely with your team to develop new diagnostic assays from concept through to validated, production-ready methods. We apply a systematic, data-driven approach to ensure your assay meets its intended purpose before moving to manufacture.
3
Do you offer small-batch or early-stage manufacturing?
Yes. We support clients from early-stage feasibility and development batches through to full commercial manufacturing of diagnostic kids and reagents. Our scalable services are designed to grow alongside your program, whether you need a single development run or ongoing supply.
4
What quality standards do you operate to?
Quality, accuracy, and reproducibility are central to everything we do. We maintain rigorous internal quality standard across all services, with manufacturing capabilities designed to meet the standards expected by early stage pharmaceutical and biotech clients.
5
Can you help with regulatory submissions?
We work closely with clients to ensure that our analytical validation, stability studies, and manufacturing outputs are documented and delivered in a manner that supports your regulatory and commercial objectives. We recommend engaging your regulatory affairs team early in the project planning process.
6
How do I get started?
Contact us via the form on our Contact page with an outline of your project requirements. Our team will respond promptly to arrange an initial consultation and assess how we can best support your objectives.