Societal CDMO is a bi-coastal contract development and manufacturing organization (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 the area of 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 the global pharmaceutical market. 

In addition to our experience in handling DEA controlled substances and developing and manufacturing modified-release dosage forms, Societal CDMO has the expertise to deliver on our clients’ pharmaceutical development and manufacturing projects, regardless of complexity level. We do all of this in our best-in-class facilities, totaling 145,000 square feet, in Gainesville, Georgia, and San Diego, California.


Pharmaceutical

Therapeutics

Societal™ CDMO

Societal™ CDMO's headquarters in San Diego, CA, United States

This department focuses on the design, maintenance, and improvement of engineering systems and facilities.

Facilities Engineering

The Scientific Research and Development team at Societal™ CDMO conducts cutting-edge research and innovation in the development of small molecule therapeutics. The team focuses on formulation, analytical development, and the creation of modified-release dosage forms, while also addressing complex manufacturing challenges. They provide critical support from pre-Investigational New Drug (IND) stages through to commercial production, ensuring regulatory compliance and optimizing drug efficacy and safety in Societal CDMO’s state-of-the-art facilities.

Scientific Research and Development

The Engineering team at Societal™ CDMO is responsible for ensuring the efficient and reliable operation of manufacturing processes and facilities. They focus on process optimization, equipment validation, automation, and maintenance to support pharmaceutical development and production. This includes developing and validating complex manufacturing systems, managing facility infrastructure, and solving technical challenges to ensure compliance with industry regulations and high-quality output.

Engineering

This department oversees the validation and auditing processes to ensure compliance with quality standards.

Quality Assurance

This department manages compliance and regulatory processes to ensure that products meet legal standards and regulations.

Regulatory Affairs

The Leadership Team at Societal™ CDMO is responsible for steering the company's strategic direction, overseeing critical operational processes, and ensuring financial stability. Comprising top executives, including the CEO, CFO, and other senior VPs, this team drives key initiatives across scientific development, supply chain management, regulatory compliance, and human resources to maintain operational excellence and achieve organizational goals in the pharmaceutical development and manufacturing industry.

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Other teams

Scientific Research and Development

Engineering

Quality Assurance

Regulatory Affairs

Leadership Team