The focus here moves from API to a dose form that can be trialled in pre-clinical studies. But, before moving to that Pre Clinical Formulation work, we can provide support that can help you make your decisions faster, and more precisely.
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The Bone substitute market has seen dramatic growth over the last few years, and is forecast to continue to grow. Our expertise has grown in line with market demand.
We have analyzed many thousands of samples, from a wide range of companies. Our expertise and ability now includes raw materials for such products, and many associated life cycle and development programmes.
Our wide range of techniques on site, experience with a range of medical device products, and GMP quality systems make us an ideal partner for any company with a launched bone substitute product, or looking to launch such a product.
Our work has included XRD, XRF, ICP-MS, ICP-OES, GC (residual solvents), SEM, Particle sizing, pH, and Surface area tests. We have developed the majority of these and validated them to meet world wide regulatory authority scrutiny.