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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
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SOPs for Dental Dosage Forms

SOP for Training of Personnel on Equipment Use

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The purpose of this SOP is to establish procedures for the training of personnel on the safe and effective use of equipment used in the manufacturing of dental dosage forms, ensuring competency and compliance with operational requirements.
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Dental Dosage Forms

SOP for Supplier Qualification for Equipment

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The purpose of this SOP is to establish procedures for the qualification of suppliers providing equipment used in the manufacturing of dental dosage forms, ensuring that equipment meets specified quality standards and regulatory requirements.
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Dental Dosage Forms

SOP for Equipment Breakdown and Repair Procedures

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The purpose of this SOP is to establish procedures for managing equipment breakdowns, initiating repair activities, and restoring equipment functionality in the manufacturing of dental dosage forms.
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Dental Dosage Forms

SOP for Equipment Logbook Maintenance

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The purpose of this SOP is to establish procedures for the maintenance of equipment logbooks used in the manufacturing of dental dosage forms, ensuring accurate recording of equipment activities and compliance with regulatory standards.
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Dental Dosage Forms

SOP for Cleaning Validation of Manufacturing Equipment

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The purpose of this SOP is to establish procedures for the cleaning validation of manufacturing equipment used in the production of dental dosage forms, ensuring that equipment is effectively cleaned to prevent cross-contamination and maintain product quality.
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Dental Dosage Forms

SOP for Process Validation of Mouthwash Manufacturing

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The purpose of this SOP is to establish procedures for the validation of the mouthwash manufacturing process used in the production of dental dosage forms, ensuring reliability, consistency, and compliance with regulatory requirements.
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Dental Dosage Forms

SOP for Process Validation of Gel Manufacturing

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The purpose of this SOP is to establish procedures for the validation of the gel manufacturing process used in the production of dental dosage forms, ensuring reproducibility, consistency, and compliance with regulatory standards.
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Dental Dosage Forms

SOP for Process Validation of Paste Manufacturing

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The purpose of this SOP is to define procedures for the validation of the paste manufacturing process used in the production of dental dosage forms, ensuring consistency, reliability, and compliance with regulatory requirements.
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Dental Dosage Forms

SOP for Temperature and Humidity Monitoring Equipment

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The purpose of this SOP is to establish procedures for the calibration, operation, and maintenance of temperature and humidity monitoring equipment used in the manufacturing environment of dental dosage forms to ensure compliance with environmental control requirements.
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Dental Dosage Forms

SOP for Stability Testing Equipment

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The purpose of this SOP is to establish procedures for the operation and maintenance of stability testing equipment used to assess the stability of dental dosage forms over time, ensuring product quality and shelf-life determination.
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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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