The use of robust analytical methods is crucial for ensuring the success of Chemistry, Manufacturing & Controls (CMC) projects. Conducting comprehensive testing using various methods is essential to guarantee the composition, safety, and effectiveness of drug products prior to and following their release.
Our proficiency in ion chromatography, osmolality, particle size determination, rheology, and viscosity uniquely equips us to support CMC. We also offer GC/FID/MS for residual solvents and volatile impurities, and when possible, we develop combined assay and impurities methods for fast and flexible analysis, ensuring the fastest turnaround times. Regulatory compliance heavily relies on analytical development, and we understand the importance of conforming to regulatory guidelines and standards. Our Z-Factor Approach guarantees dependable, precise, and resilient data to ensure the quality, safety, and efficacy of our clients’ products. At Sannova, we possess a wide range of capabilities to support stability studies, and our expertise in this area makes us a trusted partner in the pharmaceutical industry.
Partnering with Sannova gives you access to a dedicated team of analytical scientists, state-of-the-art facilities, and innovative solutions including method development or transfers and batch release testing for manufacturers. We maintain regulatory compliance, simplifying the auditing process and our rigorous internal standards based on the Z factor approach promises peace of mind. Choose Sannova for optimized analytical outcomes and overcome selection issues, accurate quantification obstacles, and source identification complexities.
Choose Sannova for exceptional quality, personalized services and excellent results, all delivered as quickly as our commitment to excellence allows.