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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Dental Dosage Forms

SOP for Continuous Training Programs for Equipment Operation

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The purpose of this SOP is to establish procedures for conducting continuous training programs aimed at enhancing the skills and knowledge of personnel involved in the operation of equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Continuous training ensures that personnel remain updated with the latest equipment advancements, operational procedures, and safety protocols.
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Dental Dosage Forms

SOP for Training Documentation for Equipment Use

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The purpose of this SOP is to establish procedures for documenting training activities related to equipment use in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Training documentation ensures that personnel are adequately trained to operate equipment safely, effectively, and in compliance with regulatory requirements.
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Dental Dosage Forms

SOP for Regulatory Submissions for Equipment Validation

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The purpose of this SOP is to define the procedures for preparing and submitting regulatory documents related to equipment validation in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Regulatory submissions ensure compliance with health authorities’ requirements and facilitate approval processes for validated equipment.
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Dental Dosage Forms

SOP for Equipment Validation Reports

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The purpose of this SOP is to define the procedures for generating equipment validation reports following the installation, operational qualification (OQ), and performance qualification (PQ) of equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Equipment validation ensures that equipment functions correctly, meets operational requirements, and complies with regulatory standards.
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Dental Dosage Forms

SOP for Cross-Contamination Prevention in Equipment Use

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The purpose of this SOP is to establish procedures for preventing cross-contamination during the use of equipment in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Effective cross-contamination prevention safeguards product quality, ensures patient safety, and complies with regulatory standards.
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Dental Dosage Forms

SOP for Personal Protective Equipment (PPE) for Equipment Operation

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The purpose of this SOP is to define the procedures for selecting, wearing, and maintaining personal protective equipment (PPE) when operating equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Proper use of PPE enhances safety, minimizes occupational hazards, and complies with regulatory requirements.
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Dental Dosage Forms

SOP for Gowning Procedures for Equipment Handling

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The purpose of this SOP is to establish procedures for gowning requirements and practices when handling equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Proper gowning procedures minimize contamination risks, maintain product quality, and ensure compliance with regulatory standards.
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Dental Dosage Forms

SOP for Equipment Performance Qualification Protocols

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The purpose of this SOP is to define the procedures for conducting equipment performance qualification (PQ) protocols to ensure that manufacturing equipment used for dental dosage forms, including pastes, gels, and mouthwashes, consistently performs according to specified requirements and regulatory standards.
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Dental Dosage Forms

SOP for Environmental Impact Assessment of Equipment

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The purpose of this SOP is to establish procedures for conducting environmental impact assessments (EIAs) of equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. EIAs ensure that equipment operations minimize environmental risks, comply with regulatory standards, and promote sustainable practices.
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Dental Dosage Forms

SOP for Equipment Lifecycle Management

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The purpose of this SOP is to establish procedures for managing the lifecycle of equipment used in the manufacturing of dental dosage forms, including pastes, gels, and mouthwashes. Equipment lifecycle management ensures optimal performance, regulatory compliance, and cost-effective maintenance throughout the equipment’s operational lifespan.
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Dental 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
  • 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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