As a leading pharmaceutical contract manufacturer, Lannett has been a trusted provider of high-quality products since 1942. Our contract manufacturing services are an integral part of our business which is evident by the fact that our customers return time and time again with new product opportunities.
At Lannett CDMO, we specialize in contract manufacturing of Oral Solid Dose (OSD), Liquids and powders including those for high potency, controlled substances and small molecule. Our platform includes:
streamlining product formulation and manufacturing from concept to commercial scale.
As a trusted pharmaceutical contract manufacturer, we have the technical expertise, industry knowledge, and state-of-the-art facilities to meet your manufacturing needs and ensure the quality and safety of your products.
We also offer support for clinical trials, including product development, manufacturing, and packaging. Our team is committed to delivering high-quality products that meet the needs of clinical trials and regulatory requirements.
Our expertise in contract development and manufacturing (CDMO) is evident in our comprehensive, prompt, experienced, adaptable, and committed approach to every project.
As a pharmaceutical contract manufacturer, we offer everything under one roof at our location in Seymour, Indiana including tech services, laboratories, manufacturing, packaging and distribution. This results in a more efficient transition between stages reducing lead times in your projects.
Thanks to our carefully crafted On-time Delivery matrix and Schedule Attainment matrix, along with quality processes in place, we consistently achieve a high success rate in schedule attainment and yield rate.
Take advantage of 75 years of deep industry knowledge in the pharmaceutical space. With over 100 unique marketed pharmaceutical products and 17 approved product applications since 2019, we confidently deliver quality services for any manufacturing need. In addition to our manufacturing capabilities, Lannett offers tech transfer services to streamline the transfer of a product from development to manufacturing. Our experienced team has the expertise to ensure a smooth and efficient transfer, minimizing any potential impact on project timelines.
The field of pharmaceuticals is evolving. This drives us to innovate processes that are agile and seamless, increasingly improving what we do while staying relevant in the market. With our streamlined operations, we also provide detailed customization according to your needs.
From formulation to commercial supply, our staff strives to ensure that product quality is met, suitable process performance is achieved, appropriate process controls are in place, improvement opportunities are identified, and the product body of knowledge is continually expanded. As your trusted CDMO partner, we are committed to delivering high-quality services for any manufacturing need.
average rate recordables per year
critical Form 483 observations
approved product applications since 2019
schedule attainment; Average product yield rate of 96%