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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Nanoparticle Formulation

Nanoparticle Formulation : SOP for Supercritical Fluid Techniques for Nanoparticle Preparation

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This SOP outlines the use of supercritical fluid techniques for the preparation of nanoparticles, which allow for controlled particle size and purity. The supercritical fluid method is commonly used to prepare drug nanoparticles with enhanced solubility.
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Nanoparticle Formulation

Nanoparticle Formulation : SOP for Emulsification-Solvent Evaporation Technique in Nanoparticle Formulations

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This SOP outlines the emulsification-solvent evaporation technique, commonly used to prepare nanoparticles for drug delivery systems. The goal is to standardize the process to ensure consistent nanoparticle size and encapsulation efficiency.
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Nanoparticle Formulation

Nanoparticle Formulation : SOP for Preparation of Nanocrystals for Drug Delivery

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This SOP describes the process for preparing drug nanocrystals, which enhance the solubility and bioavailability of poorly water-soluble drugs. The goal is to standardize the preparation of nanocrystals for drug delivery applications.
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Nanoparticle Formulation

Nanoparticle Formulation : SOP for Preparation of Metal Nanoparticles

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This SOP describes the process for preparing metal nanoparticles, such as gold, silver, and iron oxide nanoparticles, for various applications, including drug delivery, catalysis, and biomedical imaging.
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Nanoparticle Formulation

Nanoparticle Formulation : SOP for Nanoencapsulation Techniques for Drug Delivery

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This SOP outlines the standard procedures for performing nanoencapsulation techniques, commonly used in drug delivery systems to improve bioavailability and targeted delivery of pharmaceutical compounds.
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Nanoparticle Formulation

Nanoparticle Formulation : SOP for Use of Surfactants in Nanoparticle Formulations

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This SOP provides guidelines for the appropriate selection, handling, and use of surfactants in nanoparticle formulations to ensure proper stabilization of particles and consistency in product quality.
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Nanoparticle Formulation

SOP for Preparation of Polymer-Based Nanoparticles

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This SOP describes the process for preparing polymer-based nanoparticles, commonly used for drug delivery and other biomedical applications. It aims to ensure a consistent and high-quality preparation process.
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Nanoparticle Formulation

SOP for Preparation of Lipid-Based Nanoparticles

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This SOP outlines the process for preparing lipid-based nanoparticles (LNPs), which are commonly used for drug delivery systems. The objective is to standardize the preparation process, ensuring consistency and quality in the formulation.
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Nanoparticle Formulation

SOP for Weighing and Dispensing of Raw Materials for Nanoparticle Formulations

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This SOP outlines the procedures for accurately weighing and dispensing raw materials used in nanoparticle formulations. The aim is to ensure the correct quantities are measured and handled safely to avoid contamination or errors in formulation.
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Nanoparticle Formulation

SOP for Solvent Selection and Preparation for Nanoparticle Synthesis

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This SOP provides a detailed guideline for selecting, handling, and preparing solvents used in the synthesis of nanoparticle formulations. This ensures the correct solvent is chosen for the desired nanoparticle properties and that solvents are handled safely.
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Nanoparticle Formulation

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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.
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  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
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  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal 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

New Publication: A must for All.

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