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SOP for Selection and Preparation of Solvents for Lyophilized Formulations

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SOP for Selection and Preparation of Solvents for Lyophilized Formulations

Standard Operating Procedure for Solvent Selection and Preparation for Lyophilized Formulations

1) Purpose

This SOP defines the procedure for selecting and preparing solvents used in lyophilized formulations, ensuring the solvents meet the required specifications for product quality and stability.

2) Scope

This SOP applies to the selection and preparation of solvents by formulation scientists, operators, and QA teams involved in lyophilized product development.

3) Responsibilities

  • Operators: Responsible for preparing solvents as per the procedure.
  • Formulation Scientists: Responsible for selecting the appropriate solvent for each formulation.
  • QA: Responsible for verifying solvent quality and process documentation.
See also  SOP for Use of Humectants in Lyophilized Products

4) Procedure

4.1 Solvent Selection

4.1.1 Criteria for Solvent Selection

  • 4.1.1.1 The solvent should be non-reactive with active pharmaceutical ingredients (API).
  • 4.1.1.2 The solvent should facilitate efficient lyophilization.
  • 4.1.1.3 Ensure the solvent is compatible with the lyophilization equipment.
  • 4.1.1.4 The solvent must meet pharmacopoeial standards (e.g., USP, EP).

4.2 Solvent Preparation

4.2.1 Equipment Preparation

  • 4.2.1.1 Clean and calibrate measuring equipment such as volumetric flasks and graduated cylinders.
  • 4.2.1.2 Ensure that containers are properly labeled and sanitized.

4.2.2 Solvent Measurement

  • 4.2.2.1 Measure the required quantity of solvent as per the formulation guidelines.
  • 4.2.2.2 Verify the measurements with a second operator for accuracy.
See also  SOP for Preparing Lyophilized Formulations for Oral Administration

4.2.3 Mixing Procedure

  • 4.2.3.1 If necessary, mix the solvent with other excipients or solvents in the appropriate ratio.
  • 4.2.3.2 Use mechanical
stirrers if the solvent requires agitation.

5) Abbreviations

  • USP: United States Pharmacopeia
  • EP: European Pharmacopeia
  • API: Active Pharmaceutical Ingredient

6) Documents

  • Solvent Preparation Logbook

7) References

  • USP, EP standards for solvents

8) SOP Version

Version 1.0

Annexure

Solvent Preparation Logbook Template

Date Solvent Batch No. Measured Quantity Operator Initials QA Verification
DD/MM/YYYY Solvent Name Batch Number Quantity in Liters Operator Name QA Initials
           


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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
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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
  • 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
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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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