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SOP for Supplier Relationship Management

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SOP for Supplier Relationship Management

Supplier Relationship Management – Standard Operating Procedure

1) Purpose

To establish guidelines for managing relationships with suppliers to ensure consistent quality, reliability, and mutual benefit in the procurement process within the pharmaceutical purchase department.

2) Scope

This SOP applies to all activities related to maintaining and improving relationships with suppliers.

3) Responsibilities

Procurement Manager: Responsible for overseeing supplier relationship management activities.
Supplier Relationship Management (SRM) Team: Responsible for implementing and maintaining effective supplier relationship strategies.
Suppliers: Responsible for adhering to agreed-upon terms and maintaining open communication.

4) Procedure

4.1) Establishing Supplier Relationships:
4.1.1) Identify key suppliers critical to the procurement process and overall business objectives.
4.1.2) Develop a comprehensive understanding of each supplier’s business, capabilities, and objectives.

See also  Purchase Departments: SOP for Supplier Qualification and Approval

4.2) Communication:
4.2.1) Establish clear and consistent communication channels with suppliers.
4.2.2) Schedule regular meetings to discuss performance, address issues, and plan future activities.

4.3) Performance Monitoring:
4.3.1) Develop key performance indicators (KPIs) to measure supplier performance.
4.3.2) Conduct regular performance reviews based on agreed-upon metrics and provide feedback to suppliers.

4.4) Collaboration and Development:
4.4.1) Work collaboratively with suppliers to identify areas for improvement and innovation.

4.4.2) Provide support and resources to help suppliers improve their processes and capabilities.

4.5) Issue Resolution:
4.5.1) Develop a structured process for resolving disputes and issues with suppliers.
4.5.2) Ensure timely and effective resolution of issues to maintain positive relationships.

See also  SOP for Record Keeping and Documentation

4.6) Risk Management:
4.6.1) Identify potential risks in the supplier relationship and develop mitigation strategies.
4.6.2) Regularly review and update risk management plans based on changes in the supplier landscape.

4.7) Documentation and Record Keeping:
4.7.1) Maintain detailed records of all supplier interactions, performance reviews, and development activities.
4.7.2) Ensure documentation is complete, accurate, and readily available for audits and future reference.

4.8) Continuous Improvement:
4.8.1) Regularly review supplier relationship management practices and identify opportunities for improvement.
4.8.2) Implement changes to enhance the effectiveness of supplier relationship management strategies.

5) Abbreviations, if any

  • SRM: Supplier Relationship Management
  • KPI: Key Performance Indicator
See also  SOP for Ethical Procurement Practices

6) Documents, if any

  • Supplier Performance Reports
  • Meeting Minutes
  • Communication Records
  • Development Plans
  • Risk Management Plans

7) Reference, if any

Regulatory Guidelines: FDA CFR Part 211, ISO 9001:2015
Industry Standards: Best practices in supplier relationship management

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
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  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
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  • Nebulizers
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  • 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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