Regulatory Agencies require written procedures for all systems and operations which impact the quality and safety of pharmaceutical products. Standard Operating Procedures (SOP's) provide the main forum for the documentation of a Company's systems and operations. SOP's are therefore the most popular documents audited by Regulatory Agencies during GMP inspections and all too often they result in observations.
This course provides helpful information by presenting topics associated with the writing, formatting, execution and management of SOP's that contribute to consistent and efficient operations. It also discusses good documentation practices required by companies to ensure GMP compliance and relates the role which SOP's play in achieving the required level of compliance and quality.
This course provides helpful information by presenting topics associated with the writing, formatting, execution and management of SOP's that contribute to consistent and efficient operations. It also discusses good documentation practices required by companies to ensure GMP compliance and relates the role which SOP's play in achieving the required level of compliance and quality.
