Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Vendor Audits

Posted on By

Standard Operating Procedure for Vendor Audits

Purpose

The purpose of this SOP is to establish procedures for auditing and evaluating vendors and suppliers of pharmaceutical products to ensure compliance with quality standards, regulatory requirements, and contractual agreements.

Scope

This SOP applies to all personnel involved in vendor management, procurement, quality assurance, and warehouse operations within the pharmaceutical facility.

Responsibilities

  • Procurement Department: Responsible for vendor selection, contract negotiation, and vendor relationship management.
  • Quality Assurance Department: Responsible for conducting vendor audits, evaluating vendor performance, and ensuring compliance with quality standards.
  • Warehouse Managers: Responsible for implementing vendor audit procedures and ensuring that vendors comply with warehouse requirements.
  • Vendor Auditors: Responsible for planning, conducting, and documenting vendor audits in accordance with this SOP.
See also  SOP for Forklift Operations

Procedure

  1. Vendor Selection and Pre-qualification:
    • Establish criteria for vendor selection based on factors such as product quality, reliability, reputation, and compliance with regulatory requirements.
    • Conduct pre-qualification assessments of potential vendors to verify their capabilities, facilities, and compliance with applicable standards.
    • Maintain a list of approved vendors and suppliers based on pre-qualification results and ongoing performance evaluations.
  2. Vendor Audit Planning:
    • Develop a risk-based audit schedule to prioritize vendors for audit based on factors such as criticality, past performance, and regulatory requirements.
    • Define audit objectives, scope, and criteria for each audit based on the nature of the vendor’s products, services,
and associated risks.
  • Notify vendors in advance of upcoming audits and request necessary documentation and access to facilities for audit purposes.
  • Vendor Audit Execution:
    • Conduct on-site or remote audits of vendor facilities, processes, and quality management systems using standardized audit protocols and checklists.
    • Interview key personnel, observe operations, and review documentation to assess compliance with quality standards, regulatory requirements, and contractual agreements.
    • Document audit findings, observations, and non-conformities identified during the audit process, and discuss preliminary findings with vendor representatives as needed.
  • Vendor Audit Reporting and Follow-Up:
    • Prepare comprehensive audit reports summarizing audit findings, observations, and recommendations for corrective actions.
    • Review audit reports with vendor representatives to ensure mutual understanding of findings and corrective action requirements.
    • Track and monitor the implementation of corrective actions by vendors, follow up on outstanding issues, and verify the effectiveness of corrective measures through follow-up audits or inspections.
  • Abbreviations

    • SOP: Standard Operating Procedure

    Documents

    • Vendor Audit Plan
    • Audit Checklist
    • Audit Report
    • Corrective Action Plan
    • Follow-Up Audit Report

    SOP Version

    Version 1.0

    See also  SOP for Safe Material Handling Practices
    Good Warehousing Practices Tags:Disaster recovery plan for warehouse, Inventory management procedures, Pharmaceutical warehouse guidelines, Quality control in warehouse, SOP for warehouse operations, Warehouse cleanliness standards, Warehouse continuous improvement, Warehouse emergency response, Warehouse equipment maintenance, Warehouse hygiene practices, Warehouse inventory control, Warehouse maintenance SOP, Warehouse management review, Warehouse product segregation, Warehouse risk assessment, Warehouse safety protocols, Warehouse security breach response, Warehouse security measures, Warehouse SOP, Warehouse staff training

    Post navigation

    Previous Post: Good Warehousing Practices: SOP for Internal Audits
    Next Post: How often should SOP’s be reviewed and updated in pharmaceutical manufacturing?

    Standard Operating Procedures V 1.0

    • Aerosols
    • Analytical Method Development
    • Bioequivalence Bioavailability Study
    • Capsule Formulation
    • Clinical Studies
    • Creams
    • Data Integrity
    • Dental Dosage Forms
    • Drug Discovery
    • Environment, Health and Safety
    • Formulation Development
    • Gels
    • Good Distribution Practice
    • Good Warehousing Practices
    • In-Process Control
    • Injectables
    • Liquid Orals
    • Liposome and Emulsion Formulations
    • Lotions
    • Lyophilized Products
    • Maintenance Dept.
    • Medical Devices
    • Metered-Dose Inhaler
    • Microbiology Testing
    • Nanoparticle Formulation
    • Nasal Spray Formulations
    • Nebulizers
    • Ocular (Eye) Dosage Forms
    • Ointments
    • Otic (Ear) Dosage Forms
    • Pharmacovigilance
    • Powder & Granules
    • Purchase Departments
    • Quality Assurance
    • Quality Control
    • Raw Material Stores
    • Regulatory Affairs
    • Tablet Manufacturing
    • Rectal Dosage Forms
    • Transdermal Patches
    • Vaginal Dosage Forms
    • Validations and Qualifications

    Read SOPs in your Language:

     - 
    Bengali
     - 
    bn
    English
     - 
    en
    Gujarati
     - 
    gu
    Hindi
     - 
    hi
    Malayalam
     - 
    ml
    Marathi
     - 
    mr
    Punjabi
     - 
    pa
    Tamil
     - 
    ta
    Telugu
     - 
    te

    NEW! Revised SOPs – V 2.0

    • Aerosols V 2.0
    • Analytical Method Development V 2.0
    • API Manufacturing V 2.0
    • BA-BE Studies V 2.0
    • Biosimilars V 2.0
    • Capsules V 2.0
    • Creams V 2.0
    • Elixers V 2.0
    • Ointments V 2.0
    • Raw Material Warehouse V 2.0
    • Tablet Manufacturing V2.0

    New Publication: A must for All.

    Copyright © 2025 SOP Guide for Pharma.

    Powered by PressBook WordPress theme

    Go to mobile version