Sannova offers expert bioanalytical and analytical testing for drug manufacturing to ensure the quality and safety of the end product. Our services include testing API quality and purity, monitoring critical process parameters, and validating analytical methods. We also provide market access consulting and guidance for advanced therapies like cell and gene therapy. Partnering with us means addressing challenges during the manufacturing process from experience, ensuring regulatory compliance, and achieving product success in the market.

Our expert bioanalytical and analytical services help navigate any challenges or hurdles that may arise during this critical stage of therapeutic development. Partnering with us during your drug manufacturing means you benefit from the highest quality service, delivered as quickly and effectively as possible.

Chemistry, Manufacturing, and Controls (CMC) is crucial for pharmaceutical product development, ensuring quality and consistency at all stages. Analytical services play a critical role in the CMC phase, developing and implementing methods to test drug products for purity, potency, and safety. Sannova offers expert analytical support for this phase, providing accurate and reliable data to ensure regulatory compliance and patient safety. Our team of experts can help you overcome any challenges with speed, quality, and flexibility, enabling you to make informed decisions about your drug product.