GMP Deviations

Deviations in the life sciences industry refer to any departure from established procedures, specifications, or standards. These deviations can occur at various stages of the product lifecycle, including manufacturing, testing, and distribution. They can range from minor errors, such as incorrect documentation, to major incidents, such as equipment failures or product contamination. Effective deviation management involves promptly identifying, investigating, and resolving deviations to prevent recurrence and ensure product quality and safety.