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Corporate Governance

Our Responsibilities / Corporate Governance

Our Business Strategy

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.

R&D Center

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:

  1. Fast Track Process Development: We have extensive expertise in accelerating the process development timeline, allowing us to efficiently bring products from concept to commercialization. Our streamlined approach ensures optimal efficiency without compromising quality.
  1. Process Technology Transfer: We excel in transferring developed processes from one site to another seamlessly. Our experienced team is well-versed in the intricacies of technology transfer, ensuring a smooth transition and maintaining process integrity throughout.
  1. Rapid Stability Indicating Method Development: We have a strong capability to rapidly develop stability-indicating analytical methods. These methods enable us to assess product stability quickly and accurately, supporting timely decision-making during the development and manufacturing stages.
  1. Efficient Data Integration: We have implemented robust systems for data management and integration, allowing us to effectively consolidate and analyze complex data sets. This enables us to extract valuable insights and make data-driven decisions throughout the product lifecycle.
  1. Efficient Troubleshooting: Our team possesses excellent troubleshooting skills, enabling us to identify and resolve challenges swiftly. We leverage our deep technical knowledge and experience to overcome obstacles and keep projects on track.
  1. cGMP Manufacturing and ICH Guidelines: With a deep understanding of current Good Manufacturing Practices (cGMP) and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, we ensure that our manufacturing processes comply with the highest quality and regulatory standards.
  1. Program Management: We have a strong program management approach, ensuring effective coordination and communication among cross-functional teams. Our experienced program managers oversee projects from initiation to completion, ensuring milestones are met and deliverables are achieved.
  2. Delivery Strategies: We employ strategic delivery approaches to optimize efficiency and meet project timelines. Our focus on effective planning, resource allocation, and risk management ensures successful project execution.
  1. Backward Integration of Key Starting Materials: We have established backward integration capabilities for key starting materials used in commercial product manufacturing. This vertical integration enhances our supply chain efficiency, reduces dependency on external sources, and ensures reliable access to critical materials.

These core competencies reflect our commitment to excellence, innovation, and delivering high-quality pharmaceutical products and services to our clients.

Quality Control Infrastructure

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.

CDMO capabilities

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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