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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

SOP for Spill Management and Containment of Nanoparticles

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This SOP outlines the procedures for safely managing and containing spills of nanoparticles in the laboratory or production environment, ensuring that exposure is minimized and that the spill is cleaned up effectively.
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Nanoparticle Formulation

SOP for Ventilation and Environmental Controls in Nanoparticle Production Areas

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This SOP outlines the necessary ventilation and environmental controls in areas where nanoparticles are produced to minimize airborne nanoparticle exposure and ensure safe working conditions.
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Nanoparticle Formulation

SOP for Personal Protective Equipment (PPE) Requirements in Nanoparticle Production

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This SOP outlines the necessary Personal Protective Equipment (PPE) required for handling nanoparticles during production and research activities to protect personnel from potential exposure to hazardous materials.
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Nanoparticle Formulation

SOP for Safe Handling of Nanoparticles and Nanomaterials

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This SOP outlines the procedures to safely handle nanoparticles and nanomaterials in the laboratory and manufacturing environments to minimize exposure risks and ensure compliance with safety regulations.
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Nanoparticle Formulation

SOP for Risk Assessment of Nanoparticle Manufacturing Processes

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This SOP outlines the procedure for conducting a risk assessment of the manufacturing processes involving nanoparticles. The goal is to identify potential hazards, assess risks, and implement control measures to minimize exposure and ensure safety.
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Nanoparticle Formulation

SOP for Optimization of Solvent Removal Techniques in Nanoparticle Formulations

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This SOP outlines the procedure for optimizing solvent removal techniques in nanoparticle formulations, ensuring efficient evaporation of solvents while maintaining nanoparticle stability and size.
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Nanoparticle Formulation

SOP for Preparation of Nanoparticles for Brain Targeting

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This SOP outlines the procedure for preparing nanoparticles designed for brain targeting via the blood-brain barrier (BBB), enabling delivery of therapeutics to the brain with enhanced bioavailability.
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Nanoparticle Formulation

SOP for Preparation of Nanoparticles for Sublingual Administration

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This SOP outlines the procedure for preparing nanoparticles for sublingual drug delivery, allowing for rapid absorption of drugs through the mucosal tissues under the tongue, bypassing first-pass metabolism and providing faster therapeutic effects.
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Nanoparticle Formulation

SOP for Incorporation of Bioactive Molecules in Nanoparticle-Based Formulations

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This SOP outlines the procedure for incorporating bioactive molecules, such as proteins, peptides, or small molecules, into nanoparticle formulations for targeted drug delivery or therapeutic applications.
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Nanoparticle Formulation

SOP for Preparation of Inorganic Nanoparticles

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This SOP outlines the procedure for the preparation of inorganic nanoparticles, such as gold, silver, and zinc oxide nanoparticles, which are used in various biomedical, industrial, and environmental applications.
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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.
  • 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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