The Ultimate Resource for Pharmaceutical SOPs and Best Practices
SOP for Regulatory Submission and Filing Standard Operating Procedure for Regulatory Submission and Filing 1) Purpose This SOP outlines the procedures for preparing, submitting, and filing regulatory documents to regulatory authorities for approval of pharmaceutical products. 2) Scope This SOP applies to all personnel involved in regulatory affairs, including regulatory affairs managers, regulatory affairs specialists,…
SOP for Good Distribution Practices (GDP) Compliance Standard Operating Procedure for Good Distribution Practices (GDP) Compliance 1) Purpose This SOP outlines the procedures for ensuring compliance with Good Distribution Practices (GDP) to maintain the integrity, quality, and safety of pharmaceutical products throughout the distribution chain. 2) Scope This SOP applies to all personnel involved in…
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SOP for Good Clinical Practices (GCP) Compliance Standard Operating Procedure for Good Clinical Practices (GCP) Compliance 1) Purpose This SOP outlines the procedures for ensuring compliance with Good Clinical Practices (GCP) to ensure the safety, rights, and well-being of clinical trial subjects and the integrity of clinical trial data. 2) Scope This SOP applies to…
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SOP for Good Laboratory Practices (GLP) Compliance Standard Operating Procedure for Good Laboratory Practices (GLP) Compliance 1) Purpose This SOP outlines the procedures for ensuring compliance with Good Laboratory Practices (GLP) to ensure the integrity, reliability, and quality of laboratory data generated for pharmaceutical product testing and research. 2) Scope This SOP applies to all…
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SOP for Good Manufacturing Practices (GMP) Compliance Standard Operating Procedure for Good Manufacturing Practices (GMP) Compliance 1) Purpose This SOP outlines the procedures for ensuring compliance with Good Manufacturing Practices (GMP) to consistently produce pharmaceutical products that meet quality and regulatory requirements. 2) Scope This SOP applies to all personnel involved in the manufacturing, packaging,…
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SOP for Good Manufacturing Practices (GMP) Compliance Standard Operating Procedure for Good Manufacturing Practices (GMP) Compliance 1) Purpose This SOP outlines the procedures for ensuring compliance with Good Manufacturing Practices (GMP) to consistently produce pharmaceutical products that meet quality and regulatory requirements. 2) Scope This SOP applies to all personnel involved in the manufacturing, packaging,…
SOP for Hazard Analysis and Critical Control Points (HACCP) Standard Operating Procedure for Hazard Analysis and Critical Control Points (HACCP) 1) Purpose This SOP outlines the procedures for implementing and maintaining a Hazard Analysis and Critical Control Points (HACCP) system to identify, evaluate, and control hazards related to food safety within the pharmaceutical manufacturing process….
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SOP for Root Cause Analysis Standard Operating Procedure for Root Cause Analysis 1) Purpose This SOP outlines the procedures for conducting root cause analysis (RCA) to systematically investigate and identify the underlying causes of deviations, incidents, non-conformances, or other quality issues within the pharmaceutical facility. 2) Scope This SOP applies to all departments and personnel…
SOP for Continuous Improvement Programs Standard Operating Procedure for Continuous Improvement Programs 1) Purpose This SOP outlines the procedures for implementing and managing continuous improvement programs to enhance efficiency, effectiveness, and compliance within the pharmaceutical facility. 2) Scope This SOP applies to all departments and personnel involved in identifying, implementing, and monitoring continuous improvement initiatives…
SOP for Quality Metrics and Reporting Standard Operating Procedure for Quality Metrics and Reporting 1) Purpose This SOP outlines the procedures for establishing, measuring, analyzing, and reporting quality metrics to monitor and improve processes, products, and systems within the pharmaceutical facility. 2) Scope This SOP applies to all departments and personnel involved in the collection,…