Clinical Supply Sourcing Center
Successfully navigating the complexities of the clinical supply chain can eliminate delays and lead to sponsors bringing their drugs to market faster.
The logistics are complicated by regulatory requirements specific to geography, changes to import/export regulations, and specialized handling and temperature controls for biologic materials. For drug sponsors, there are specialized service providers that include fully-integrated logistics services, life science-focused couriers, transportation companies with healthcare offerings, and cargo handlers. All can be aligned to manage the storage and distribution of clinical materials.
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Clinical Supply CMOs
Abzena is the leading end-to-end bioconjugate and complex biologics CDMO + CRO. From discovery through commercial launch, we support customers with fully integrated programs or individual services designed to de-risk and streamline the development of new treatments for patients in need. Abzena develops and implements innovative solutions that enable biotech and biopharma companies to realize the full potential of their molecule.
For over 25 years, Altasciences has offered drug development, manufacturing, and analytical services to pharmaceutical and biotech companies worldwide, including formulation development, Phase I through commercial manufacturing, and ICH stability storage and testing. As an extension of our clients' teams, we actively collaborate with them throughout the entire development and manufacturing process. Using advanced methods, we have manufactured nearly every pharmaceutical dosage form on the market.
Ascendia Pharmaceuticals is a specialty pharmaceutical CDMO that provides custom sterile- and non-sterile-enabling formulations and manufacturing, along with analytical methods for new chemical entities, complex dosage forms, and 505(B)(2) product development, as well as OTCs, nutraceuticals, and animal health.
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a growing team of over 2,200 experts servicing global clients from North America and European sites, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
With the mission of providing state-of-the-art education, training and contract services in the fast-emerging field of biopharmaceutical processing, Jefferson Institute for Bioprocessing (JIB) formally opened its doors in 2019 and is the first—and only—specialized education, training and CDMO for biopharmaceutical processing in North America. JIB's 25,000 sq. ft fully closed-processing, CNC, GMP-simulated pilot scale and process development facility houses ready-to-use technologies in fully flexible, ballroom designed suites.
Kymanox is a life science professional services organization that offers engineering, scientific, and compliance support to companies exclusively in the biotechnology, pharmaceutical, medical device, and combination product industries. With its diverse team, Kymanox helps clients navigate commercialization challenges that arise throughout a product's lifecycle – from early development to post-market commercialization – with optimized safety, quality, efficacy, and accessibility.
Thermo Fisher Scientific's Patheon provides industry-leading pharma services solutions for drug development, clinical trial logistics and commercial manufacturing to customers of all sizes.
PCI Pharma Services is an integrated full service provider, a proven and trusted partner to leading companies in the global healthcare industry. We offer unparalleled expertise and experience in taking compounds from the earliest stages of development through to successful commercialization, delivering speed-to-market and commercial success for our customers.
Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway for small molecule & peptide drug programs. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients.
Specializing in small batch aseptic fill/finish of vials, syringes, and cartridges, Singota Solutions is focused on moving products through the drug development pipeline faster—with agility, accountability, and transparency.
Societal™ CDMO is a bi-coastal CDMO with capabilities spanning pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms with a primary focus in small molecules. With an expertise in solving complex manufacturing problems, Societal is a leading CDMO providing therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging and logistics services to the global pharmaceutical market.