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SOP for Vendor Audit and Evaluation

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SOP for Vendor Audit and Evaluation

Vendor Audit and Evaluation – Standard Operating Procedure

1) Purpose

To establish guidelines for conducting vendor audits and evaluations to ensure compliance with quality and regulatory requirements.

2) Scope

This SOP applies to all vendor audit and evaluation activities conducted by the pharmaceutical purchase department.

3) Responsibilities

Quality Assurance Team: Responsible for planning and conducting vendor audits.
Purchasing Team: Responsible for coordinating evaluations and maintaining vendor records.

4) Procedure

4.1) Audit Planning:
4.1.1) Identify vendors to be audited based on risk assessment.
4.1.2) Develop audit plans including objectives and scope.

See also  SOP for Vendor Selection Criteria

4.2) Conducting Audits:
4.2.1) Schedule audits with vendors and notify them in advance.
4.2.2) Perform on-site audits according to the audit plan.

4.3) Audit Reporting:
4.3.1) Document audit findings, observations, and non-conformances.
4.3.2) Prepare audit reports for review and approval.

4.4) Corrective Actions:
4.4.1) Issue corrective action requests (CARs) for identified non-conformances.
4.4.2) Monitor and verify effectiveness of corrective actions.

4.5) Vendor Performance Evaluation:
4.5.1) Evaluate vendor performance based on audit results and other criteria.
4.5.2) Maintain vendor performance records and update as necessary.

5) Abbreviations, if any

N/A

6)

Documents, if any
  • Audit Plans
  • Audit Reports
  • Corrective Action Reports
  • Vendor Performance Scorecards

7) Reference, if any

Regulatory Guidelines: FDA CFR Part 820, ICH Q9
Industry Standards: ISO 13485:2016

8) SOP Version

Version 1.0

Purchase Departments Tags:Contract negotiation SOP, Emergency purchase procedure SOP, Goods receiving process SOP, Handling expired materials SOP, Inventory management SOP, Laboratory supplies procurement SOP, Manufacturing equipment procurement SOP, Material inspection SOP, Material specification SOP, Minimum stock level SOP, Order confirmation SOP, Packaging material procurement SOP, Pharmaceutical purchase SOP, Purchase return process SOP, Raw material procurement SOP, SOP for purchase order creation, SOP for purchase requisition, SOP for supplier qualification, SOP for vendor audit, Stock replenishment planning SOP, Supplier corrective action SOP, Supplier non-conformance SOP, Supplier performance monitoring SOP, Vendor communication protocol SOP, Vendor selection criteria SOP

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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

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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.

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