Fill Finish Services CMO Sourcing Center
Fill/Finish is typically the last step of the injectable drug manufacturing process. It’s considered to be the most critical and specialized aspect of manufacturing such drugs, and can often be a limiting step in terms of the rate at which product can reach clinical trials or markets.
Fill/Finish activities are subject to extreme scrutiny by regulatory agencies and tend to be a costly step in the manufacturing process. Fill/Finish providers can offer specialized services in such areas as the types of primary packaging containers used (ampoules, cartridges, syringes and vials), types of biologics, and scale of operation (preclinical, clinical and commercial).
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Fill Finish Services CMOs
When you engage AbbVie Contract Manufacturing, you're getting more than a CMO. You access the capabilities of a highly experienced biopharmaceutical company. You know that your project will benefit from our broad range of capabilities and portfolio of state-of-the-art facilities. Most of all, you know that your project will be reliably served by a business with a trusted reputation for innovation, reliability, compliance and delivery.
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.
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.
For 25 years Aldevron has been a catalyst, advancing therapeutic and vaccine development through expert plasmid DNA, RNA, and protein custom manufacturing, supporting our clients from discovery to commercialization. Our custom CDMO services have given scientists around the world essential components to accelerate their research and make a difference. Whether you're working on a gene therapy, cell therapy, or vaccine development, it starts with a high-quality DNA, RNA, or Protein.
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.
August Bioservices is a growing, US-based CDMO, focused on sterile injectable formulation and fill/finish cGMP manufacturing — optimizing liquid and lyo products, aseptic or terminally sterilized — at both clinical and commercial scale. As a "one stop CDMO shop," we offer turnkey, end-to-end services, and integrated project teams all onsite, under one roof.
B. Braun's OEM Division delivers complete contract manufacturing capabilities for a multitude of markets including surgical, pharmaceutical, and biotech. The B. Braun OEM Division has the in-house capabilities, project management approach, and lean manufacturing practices to take your designs from concept to delivery. And through our Sharing Expertise® initiative, you have immediate access to B. Braun's renowned manufacturing and engineering capabilities.
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.
FUJIFILM Diosynth Biotechnologies is a CDMO Partner for Life. We combine technical leadership in cell culture, microbial fermentation and advanced therapies with world class cGMP manufacturing facilities and superior program management to advance tomorrow's medicines.
IDT Biologika is a global CDMO for Innovative Vaccines, Cell & Gene Therapeutics and Aseptic Fill-Finish of other biologics. We offer clients a single source CDMO partner at our sites in Germany and the USA, with seamless end-to-end solutions and the ability to nimbly scale projects from development through to commercialization. This includes Process Development, Drug Substance Manufacturing, Sterile Dosage Fill-Finish, Labelling & Packaging, Quality Control & Analytics.
INCOG has been designed and built from decades of experience with a clear purpose: to deliver better CDMO services in the injectable drug product space. The company's service offering includes filling drug product into vials, syringes, and cartridges. INCOG also offers support services to include formulation development, analytical development, stability testing and storage, and final inspection, labeling, packaging, and device assembly.
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 a preferred global partner to the pharmaceutical, biotech and nutrition markets. We work to enable a healthier world by supporting our customers to deliver new and innovative medicines that help treat a wide range of diseases. We achieve this by combining technological insight with world-class manufacturing, scientific expertise and process excellence. Our unparalleled breadth of offerings enables our customers to commercialize their discoveries and innovations in the healthcare industry.
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.
Resilience is a manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption. Founded in 2020, the company is building a sustainable network of high-tech, end-to-end manufacturing solutions with the aim to ensure the medicines of today and tomorrow can be made quickly, safely, and at scale. Resilience seeks to offer regulatory capabilities and flexible and adaptive facilities to serve partners of all sizes.
Simtra BioPharma Solutions partners with pharmaceutical and biotech companies to support their commercialization objectives by providing scientific expertise, sterile contract manufacturing solutions, and customized support services needed to meet the unique challenges that parenteral products face.
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.
SMC Ltd. provides world-class device contract manufacturing with complete services for the Drug Delivery, Diagnostics, and Medical Device markets. Concept through commercialization services include: design, device development, manufacturing of clinical trials, and commercial scalable manufacturing. Services also include integration of filled primary drug containers with secondary packaging and distribution. Our global facilities are ISO 13485 certified, FDA registered, cGMP and Part 4 compliant.
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.
Established in 1949, Stevanato Group is the world's largest, privately-owned designer and producer of glass containers for the pharmaceutical industry. The Group comprises a wide set of capabilities dedicated to serving the biopharmaceutical and diagnostic industries: from glass containers with its historical brand Ompi, to high-precision plastic diagnostic and medical components, to contract manufacturing for drug delivery devices, to vision inspection systems, assembly, and packaging equipment.