Product development in 503B outsourcing facilities involves a detailed, highly regulated process. Every compounded medication produced by facilities like SCA Pharma must be safe, compliant, and aligned with the needs of healthcare institutions. This blog dives deeper into the product development process, covering each phase from discovery to post-launch monitoring.
The Product Development Process
The development of compounded medications requires diligence and precision. Every step ensures adherence to regulatory guidelines, such as current Good Manufacturing Practice (cGMP) regulations outlined by the FDA, and guarantees the utility and safety of the product for healthcare providers. Below is a detailed look at the five vital stages that SCA Pharma follows when creating new products. Read More >
