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SOP for Supplier Performance Monitoring

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SOP for Supplier Performance Monitoring

Supplier Performance Monitoring – Standard Operating Procedure

1) Purpose

To establish a systematic approach for monitoring and evaluating the performance of suppliers to ensure continuous improvement and compliance with agreed-upon standards.

2) Scope

This SOP applies to the monitoring of supplier performance within the pharmaceutical purchase department.

3) Responsibilities

Procurement Manager: Responsible for overseeing supplier performance monitoring.
Purchasing Team: Responsible for conducting evaluations and providing feedback.

4) Procedure

4.1) Performance Metrics Definition:
4.1.1) Define key performance indicators (KPIs) such as quality, delivery time, and responsiveness.
4.1.2) Establish benchmarks or targets for each metric.

See also  SOP for Emergency Purchase Procedure

4.2) Data Collection:
4.2.1) Collect performance data from various sources, including feedback from internal stakeholders and performance reports.
4.2.2) Ensure data accuracy and completeness.

4.3) Performance Evaluation:
4.3.1) Analyze collected data against predefined metrics and benchmarks.
4.3.2) Identify trends, strengths, and areas for improvement.

4.4) Performance Review Meetings:
4.4.1) Schedule periodic meetings with suppliers to discuss performance.
4.4.2) Provide constructive feedback and address any performance issues.

4.5) Performance Improvement Plans:
4.5.1) Collaborate with suppliers to develop improvement plans if performance falls below expectations.
4.5.2) Monitor

implementation and effectiveness of improvement actions.

5) Abbreviations, if any

N/A

6) Documents, if any

  • Supplier Performance Reports
  • Performance Evaluation Forms
  • Performance Improvement Plans
See also  SOP for Training

7) Reference, if any

Regulatory Guidelines: FDA CFR Part 211.84, ICH Q10
Industry Standards: ISO 9001:2015

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
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  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
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  • Microbiology Testing
  • Nanoparticle Formulation
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  • Nebulizers
  • Ocular (Eye) Dosage Forms
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  • 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

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