Expertise. Focus. Experience. These are the qualities of our Product Development Services team at CPL. Our team consists of more than 25 scientists with decades of formulation and analytical experience, supporting numerous NDAs, ANDAs, and 505(b)2s. The team lends its experience to overcome the challenges unique to the development of semi-solid and liquid pharmaceutical products and brings their expertise to support each and every product.
Services include formulation, process development and optimization, analytical method development and validation, packaging compatibility studies, clinical trial supplies manufacturing and filling, and scale-up. Excipient compatibility, in vitro release testing (IVRT), and forced degradation studies are important pieces of CPL's early formulation development efforts.<
CPL has state-of-the-art pre-formulation, formulation, and analytical testing equipment, including a GMP suite for scale-up and clinical trial material manufacturing and filling. The facilities can accommodate light-sensitive and oxygen-sensitive molecules, high alcohol-containing formulations, as well as hormones and steroids.
CPL has extensive experience in developing the following non-sterile dosage forms:
- Oral Suspensions
- Nasal sprays
- Topical liquid sprays