Our business strategy involves forming strategic partnerships where we hold directorship and actively participate in the operations. While our manufacturing partners handle the infrastructures, operations, and environmental health and safety of specific sites, we collaborate closely to ensure a robust quality management system. By working together, we can effectively manage and maintain the highest standards of quality throughout the entire process, ensuring the delivery of safe and reliable pharmaceutical products to our customers. Our partnership approach allows us to leverage the expertise and resources of our manufacturing partners while maintaining a strong focus on quality management.
Our R&D center boasts a spacious area of 20,000 square feet, providing ample room for conducting our research and development activities. With 45 fume hoods and a team of 60 chemists, including analytical experts, we have the capacity to carry out diverse projects simultaneously. The ratio of Ph.D. holders to M.Sc. graduates is 1:5, ensuring a strong blend of advanced expertise and practical knowledge.
Our center is fully equipped with state-of-the-art analytical instruments, which are essential for method development and release testing. We have a dedicated development laboratory equipped with stability chambers, allowing us to conduct stability studies and evaluate the performance of our formulations at an early stage. Additionally, our quality control labs also feature stability chambers, enabling us to ensure the quality and stability of our products throughout their lifecycle.
One of our core competencies lies in fast track process development and seamless technology transfer. Our experienced team specializes in efficiently transferring processes from one site to another. Moreover, we prioritize rapid stability verification, allowing us to quickly assess the stability of our products and make informed decisions during the development phase.
These capabilities serve as key differentiators, setting us apart from others in the industry. By leveraging our strengths in process development, technology transfer, and rapid stability verification, we ensure that our products meet the highest standards of quality, time-efficiency, and stability.
Our company possesses several core competencies that set us apart in the industry and enable us to deliver exceptional results for our clients. These competencies include:
These core competencies reflect our commitment to excellence, innovation, and delivering high-quality pharmaceutical products and services to our clients.
At our Quality Control Infrastructure, we prioritize rigorous testing and analysis to ensure the highest standards of quality and safety for our pharmaceutical products. Our capabilities include conducting Extractable & Leachable projects, where we thoroughly assess potential substances that may be released from packaging or manufacturing materials. We also perform Stability samples exposure and analysis to evaluate the integrity and shelf-life of our products over time. In addition, our team specializes in the characterization of Excipients/API/FDF samples, ensuring their quality and compatibility in formulations. We are adept at identifying and characterizing impurities, both known and unknown, to maintain the purity of our products. Our Working / reference standards characterization procedures enable us to establish reliable benchmarks for accurate testing and validation. Furthermore, we conduct Specific surface area analysis to assess the physical properties of our products. Through packing material testing utilizing techniques such as DSC and FTIR with ATR, we ensure the quality and suitability of our packaging materials. For injectable preparations, we meticulously analyze Osmolality and perform sub-visible particle count assessments. Additionally, we employ DVS and Water activity studies to evaluate the moisture content and stability of our formulations. Our Quality Control Infrastructure is committed to upholding stringent quality standards and ensuring the safety and efficacy of our pharmaceuticals.
Our comprehensive CDMO capabilities and state-of-the-art facilities enable us to provide a wide range of services to meet your pharmaceutical needs. With our end-to-end service approach, we focus on delivering tangible results and meeting project milestones. Our program management ensures efficient coordination and execution of projects. We have a robust quality management system in place, ensuring that our processes adhere to the highest standards of quality. We prioritize health, safety, and environmental considerations in all our operations. Data integrity and intellectual property management are core aspects of our business, ensuring confidentiality and protection of your valuable information. We offer two distinct business models to accommodate different partnership requirements.
At Teadus Pharma, our goal is to provide our clients with exceptional technical expertise, grounded in our specialist chemistry knowledge and robust project management capabilities. We are committed to delivering excellence, guided by internationally recognized ethical and quality standards.
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