Our Services

At Singota Solutions, we specialize in comprehensive and flexible Contract Development and Manufacturing Organization (CDMO) services tailored to meet the unique needs of our clients in the pharmaceutical industry. Our dedicated team is proficient in a wide array of services, including small batch aseptic filler capabilities, aseptic manufacturing solutions, and injectable formulation development. Whether it’s formulating small or large molecules such as peptides, proteins, mAbs, biosimilars, vaccines, or oligonucleotides/RNA, we excel in addressing critical aspects such as solubility, stability, pH, buffer selection, osmolality, and excipient selection. Additionally, our expertise extends to lyophilization process characterization, pre-manufacturing studies, temperature hold testing, hydrogen peroxide exposure degradation studies, pump parameter evaluation, viscosity characteristics assessment, and material compatibility testing. With a focus on innovation and quality, Singota Solutions is committed to accelerating the development of parenteral formulations while ensuring compliance with regulatory standards and meeting our clients’ specific project objectives.