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Injectables: SOP for Raw Material Testing and Approval

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SOP for Raw Material Testing and Approval

Standard Operating Procedure for Raw Material Testing and Approval

1) Purpose

The purpose of this SOP is to establish the procedure for the testing and approval of raw materials to ensure they meet the required quality standards before being used in the manufacturing process.

2) Scope

This SOP applies to all raw materials received at [Company Name] for the manufacturing of intramuscular, subcutaneous, and intravenous injection products.

3) Responsibilities

The responsibilities of this SOP include:
– Quality Control (QC) Department: Conducting tests on raw material samples.
– Quality Assurance (QA) Department: Reviewing test results and approving raw materials for use.
– Warehouse Personnel: Handling and storing raw materials during the testing process.

See also  SOP for Internal Audits of Manufacturing Processes

4) Procedure

4.1 Sampling of Raw Materials
4.1.1 Upon receipt, raw materials are sampled according to the sampling plan.
4.1.2 Samples are labeled with the material name, batch number, and date of sampling.
4.2 Testing of Raw Materials
4.2.1 The QC Department conducts tests according to established methods and specifications.
4.2.2 Tests may include identity, purity, potency, and other relevant quality attributes.
4.2.3 Record all test results and observations in the laboratory notebook or electronic system.
4.3 Approval of Raw Materials
4.3.1 The QA Department reviews test results and compares

them with the acceptance criteria.
4.3.2 If the raw materials meet the specified criteria, they are approved for use.
4.3.3 Approved materials are tagged with an “Approved” label and moved to the storage area.
4.3.4 If materials fail to meet the criteria, they are rejected and quarantined for further investigation or return to the supplier.
4.4 Documentation and Records
4.4.1 Maintain records of sampling, testing, and approval/rejection of raw materials.
4.4.2 All documentation must be signed and dated by the responsible personnel.

See also  SOP for Control of Non-Conforming Materials

5) Abbreviations, if any

– QC: Quality Control
– QA: Quality Assurance

6) Documents, if any

– Sampling Plan
– Laboratory Notebook/Electronic System
– Test Methods and Specifications
– Approval/Rejection Tags

7) Reference, if any

– Good Manufacturing Practices (GMP) Guidelines
– International Organization for Standardization (ISO) Standards

8) SOP Version

Version 1.0

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Next Post: SOP for Personnel Hygiene Practices in Ointment Formulation

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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