Small Molecule Drug Product Sourcing Center
Culminating in the discovery, early development and processing work, your drug product development and manufacture – “finished dosage form” – now needs to take shape ...
as a tablet, capsule, solution, etc. and combine your API, incipients and perhaps other inactive ingredients. And as the variety and complexity of new chemical entities (NCE) continues to grow, there is stiff competition for small-molecule drug-product services. For biotechs as well as established pharma, it can be said it is never too early to start thinking about your drug product and drug-product processes and partner.
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Small Molecule Drug Product CMOs
Adare Pharma Solutions is a global technology-driven CDMO providing turnkey product development through commercial manufacturing expertise focused on oral dosage forms for the Pharmaceutical, Animal Health, and OTC markets. Adare's specialized technology platforms provide taste masking, ODTs, and customized drug-release solutions. With a proven history in drug delivery, Adare has developed and manufactured more than 40 products sold by customers in over 100 countries globally.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) committed to delivering the highest standard of service and collaboration to our clients and partners as we work side-by-side to help bring their products to patients across the globe. We offer world-class development and manufacturing services of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA) viral vectors, and genetically engineered cells.
Working with Ajinomoto Bio-Pharma Services, you get a trusted CDMO partner that has the power to make your every challenge our own, sharing your unwavering tenacity and dedication from pre-clinical program to commercial successes. We leverage our broad range of capabilities and services at our sites in Belgium, India, Japan, and the US to support your program goals.
Aragen Bioscience, Inc. is focused on accelerating antibody and other biologic product development. Our integrated preclinical research offerings include: stable cell line development, recombinant protein production and purification, antibody discovery, as well as cell-based assays and in vivo models-of-disease.
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.
For over 20 years, Asymchem has been positioned and structured to act as a true partner for pharmaceutical and biotech companies worldwide by offering integrated solutions across all stages of drug development and into commercialization.
As a CDMO with 8 state-of-the-art manufacturing sites, Asymchem's breadth of capabilities spans conventional batch manufacturing, and we are a world leader in green chemistry.
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.
Catalent is a global leader in providing integrated services, superior drug delivery technologies and manufacturing solutions to help life science innovators develop and launch successful pharmaceuticals, biologics and consumer health products.
Evonik serves as a global development partner and solutions provider to biotechnology companies to help them transform complexity into value. We bring together a broad, versatile range of core competencies, a trusted global network of sites, and strong technical expertise to support you in the development, scale-up, and manufacturing of biopharmaceutical products.
Jubilant HollisterStier is an integrated contract manufacturer of sterile injectables, ophthalmics, otics and sterile and non-sterile topicals and liquids. Our facilities in North America provide specialized manufacturing for the pharmaceutical and biopharmaceutical industries. We provide a full-range of support and services to streamline the manufacturing process such as on-site assistance from process qualifications through product release.
Headquartered outside St. Paul, Minnesota, Kindeva Drug Delivery is a leading global contract development and manufacturing organization (CDMO) in the pharmaceutical industry. Kindeva provides unique technologies and quality services to its customers, ranging from formulation and product development to commercial manufacturing. Kindeva focuses on complex drug programs, and its current offering spans inhalation drug delivery, transdermal drug delivery, microstructured transdermal systems (microsystems), and connected drug delivery.
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.
Lonza is one of the world’s most renowned companies for contract development and manufacturing, Lonza Pharma & Biotech is recognized for our reliable, high-quality services, our global capacity, our innovative technology platforms, and our extensive experience.
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.
Pfizer CentreOne is a global CDMO embedded within Pfizer and a leading supplier of specialty APIs.
Working together with our customers, we combine our knowledge with open dialogue to solve challenges.
Pharmaceutics International, Inc. (Pii) is a premier Contract Development and Manufacturing Organization (CDMO), offering unparalleled scientific insight and depth of product knowledge, while supplying high quality dosage forms that enhance the lives of patients worldwide.
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.
Sharp offers wide variety of primary and secondary packaging services for pharmaceutical and biopharma products. Our extensive range of contract services includes blistering, bottling, pouching and the assembly, labeling and packaging of injectable presentations. We offer the expertise needed to support clients with packaging design, serialization, cold chain (2-8°C) storage and distribution. Additionally, our Qualified Person (QP) services assist clients with European market release.
Syngene provides Formulation Development services for oral solid, liquid, parenteral & semi-solid dosage forms. Our end-to-end, development services range from early phase development to clinical supplies for new chemical entities, generics, paediatrics & life-cycle extension products such as 505(b)2. Our services encompass pre-formulation studies, toxicology formulation, formulation development, analytical method development and validation, process optimization and scale-up, ICH stability studies and regulatory dossier preparation.