Are you aiming to advance your project with reduced risk and enhanced efficiency? Do you want to overcome the complexities of clinical development and simplify the process from initial discovery to post-approval? Our expert team at Subduceswwi is ready to guide you every step of the way.
Our integrated consulting services seamlessly combine clinical development strategies with regulatory expertise, tailored clinical and R&D consulting, and personalized Phase I-IV study designs. By leveraging the comprehensive knowledge of Subduceswwi’s global network, we enhance your product’s potential for success.
Biostatistics
Clinical pharmacology & pharmacokinetics
Chemistry, manufacturing & control (CMC)
Clinical science
Clinical development
Regulatory strategy
Toxicology
We work closely with you to identify the optimal path forward, delivering customized regulatory, clinical development, and evidence generation strategies to fit your needs.
We bring seasoned product development expertise, collaborating with you to define and deliver the right solutions at the right time.
We are your partner, asking targeted questions to understand the full scope of your product’s needs — from regulatory requirements to medical affairs and market access. This ensures informed decisions aligned with your business goals.
We act as a true extension of your team, enhancing and applying our knowledge at every phase of your product’s journey.
We build the right team, combining clinical scientists, regulatory consultants, toxicologists, pharmacologists, biostatisticians, and other specialists to craft a clear development roadmap.
As a global consulting provider, Subduceswwi offers unparalleled expertise strengthened by our extensive global network. From early-stage discovery through post-marketing strategies, our experts work with you to ensure efficient development and improved patient outcomes. By combining scientific insight with regulatory expertise, we create comprehensive development plans tailored to your product’s unique journey.
We are the only consultancy offering a truly integrated, end-to-end solution for clinical development, ensuring smooth transitions between regulatory strategies, clinical development, and market access.
Our expert multidisciplinary team brings scientific and regulatory insights across all development phases, with a deep understanding of key stakeholders — including investors, partners, regulators, payers, providers, and patients.
Regulatory pathway navigation Guiding you through regulatory requirements and interactions, from pre-IND to post-approval.
Comprehensive development delivery Ensuring timely execution of key milestones through customized strategic planning.
Development strategy planning Crafting clear development strategies to navigate complex regulatory landscapes and emerging markets.
Managing complex product development Addressing unique needs for advanced therapies, orphan drugs, rare diseases, and compliance challenges.
Manufacturing support Providing seamless “team-in-place” solutions for both API and drug product manufacturing, including technology transfers, troubleshooting, scientific reviews, and more.