Clinical Supplies

Clinical trial supplies services encompass a wide range of activities essential for the successful execution of clinical trials. These services include:

Development and Manufacturing
As a global CDMO with sites in Germany and the US, we have extensive experience in developing and manufacturing new products for the pharmaceutical market. Our services focus on solid oral dosage forms such as powders, pellets, micropellets, or granules.
Optimizing Formulations
Our experts optimize formulations and evaluate processes to improve drug products, ensuring clinical trial success by meeting requirements for speed and budget.
Placebo Production
Placebo production is inevitable for clinical trials and should be considered during development to meet study design and timelines.
Blinding, Packaging, and Labeling
Our CTS services include the blinding, packaging, and labeling of semi-solids, liquids, and medical devices. We can organize primary and secondary packaging and labeling in both Europe and the US, including late-stage labeling capacities.
Project Management
Our dedicated and agile project management team reflects the flexibility required to meet the complex needs of global clinical trials from early Phase I to multinational Phase IV studies.
Customized Packaging
We offer customized packaging requests, including consulting services to find the most optimal study packaging design.
Storage and Distribution
We provide ambient, cold chain, and ultra-cold chain packaging, labeling, storage, and distribution capabilities. A global network of GMP storage and distribution hubs, IRT technology, and supporting services round off our portfolio.
Comparator / Co-Medication sourcing
As a leading service provider, we take pride in offering comprehensive Comparator and Co-Medication sourcing services. Our efficient sourcing solutions ensure that pharmaceutical companies can obtain high-quality comparators and co-medications seamlessly, meeting all regulatory standards. This service significantly reduces the time and effort required for procurement, allowing our clients to focus on their core research and development activities.
IOR Services
Our Importer of Record (IOR) Services are designed to simplify the complex regulatory landscape of importing pharmaceutical products. With our expert IOR services, clients experience seamless and compliant import processes, expediting product launches and ensuring adherence to all necessary regulations. This not only enhances market presence but also boosts customer satisfaction.

These services ensure that all aspects of clinical trials are covered, from development and manufacturing to packaging, labeling, storage, and distribution.