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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: SOP for otic formulation development

SOP for Labeling Machine

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SOP for Labeling Machine Standard Operating Procedure for Using Labeling Machine 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the labeling machine used in the pharmaceutical manufacturing of otic dosage forms to ensure accurate labeling of product containers. 2) Scope This SOP applies to…

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Otic (Ear) Dosage Forms

SOP for Cartoning Machine

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SOP for Cartoning Machine Standard Operating Procedure for Using Cartoning Machine 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the cartoning machine used in the pharmaceutical manufacturing of otic dosage forms to automate the packaging of blister packs into cartons. 2) Scope This SOP…

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Otic (Ear) Dosage Forms

SOP for Blister Packing Machine

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SOP for Blister Packing Machine Standard Operating Procedure for Using Blister Packing Machine 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the blister packing machine used in the pharmaceutical manufacturing of otic dosage forms to ensure accurate packaging of individual doses. 2) Scope This…

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Otic (Ear) Dosage Forms

SOP for Lyophilizer

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SOP for Lyophilizer Standard Operating Procedure for Using Lyophilizer 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the lyophilizer used in the manufacturing of otic dosage forms to preserve sensitive materials by freeze-drying. 2) Scope This SOP applies to all personnel involved in the…

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Otic (Ear) Dosage Forms

SOP for Spray Dryer

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SOP for Spray Dryer Standard Operating Procedure for Using Spray Dryer 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the spray dryer used in the manufacturing of otic dosage forms to convert liquid formulations into dry powder form. 2) Scope This SOP applies to…

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Otic (Ear) Dosage Forms

SOP for Ultrasonic Cleaner

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SOP for Ultrasonic Cleaner Standard Operating Procedure for Using Ultrasonic Cleaner 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the ultrasonic cleaner used in the manufacturing of otic dosage forms to ensure thorough cleaning of small parts and equipment. 2) Scope This SOP applies…

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Otic (Ear) Dosage Forms

SOP for Incubator

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SOP for Incubator Standard Operating Procedure for Using Incubator 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the incubator used in the manufacturing of otic dosage forms to ensure optimal conditions for microbial growth or product stability testing. 2) Scope This SOP applies to…

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Otic (Ear) Dosage Forms

SOP for Planetary Mixer

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SOP for Planetary Mixer Standard Operating Procedure for Using Planetary Mixer 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the planetary mixer used in the manufacturing of otic dosage forms to ensure thorough mixing of semi-solid and viscous products. 2) Scope This SOP applies…

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Otic (Ear) Dosage Forms

SOP for Vortex Mixer

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SOP for Vortex Mixer Standard Operating Procedure for Using Vortex Mixer 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the vortex mixer used in the manufacturing of otic dosage forms to ensure effective mixing of liquid products. 2) Scope This SOP applies to all…

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Otic (Ear) Dosage Forms

SOP for Tube Filling Machine

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SOP for Tube Filling Machine Standard Operating Procedure for Using Tube Filling Machine 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the tube filling machine used in the manufacturing of otic dosage forms to ensure accurate and consistent filling of tubes. 2) Scope This…

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Otic (Ear) Dosage Forms

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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
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Capsules V 2.0
  • Creams 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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