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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 Cleanroom Maintenance

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The purpose of this SOP is to establish procedures for the maintenance of cleanrooms used in the manufacturing of dental dosage forms to ensure cleanliness and compliance with regulatory standards.
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Dental Dosage Forms

SOP for Compressed Air System Maintenance

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The purpose of this SOP is to establish procedures for the maintenance of compressed air systems used in the manufacturing of dental dosage forms to ensure air quality and compliance with regulatory standards.
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Dental Dosage Forms

SOP for Water System Maintenance

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The purpose of this SOP is to establish procedures for the maintenance of water systems used in the manufacturing of dental dosage forms to ensure water quality and compliance with regulatory standards.
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Dental Dosage Forms

SOP for HVAC System Maintenance

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The purpose of this SOP is to establish procedures for the maintenance of HVAC (Heating, Ventilation, and Air Conditioning) systems in manufacturing areas involved in the production of dental dosage forms to ensure proper functioning and compliance with environmental control requirements.
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Dental Dosage Forms

SOP for Environmental Monitoring of Manufacturing Areas

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The purpose of this SOP is to establish procedures for environmental monitoring of manufacturing areas involved in the production of dental dosage forms to ensure cleanliness and compliance with regulatory standards.
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Dental Dosage Forms

SOP for Cleaning and Sanitization of Packaging Equipment

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The purpose of this SOP is to provide guidelines for the cleaning and sanitization of packaging equipment used in the final packaging of dental dosage forms to prevent cross-contamination and ensure product quality and safety.
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Dental Dosage Forms

SOP for Cleaning and Sanitization of Filling Machines

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The purpose of this SOP is to provide guidelines for the cleaning and sanitization of filling machines used in the manufacturing of dental dosage forms to prevent cross-contamination and ensure product quality and safety.
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Dental Dosage Forms

SOP for Cleaning and Sanitization of Mixing Equipment

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The purpose of this SOP is to provide guidelines for the cleaning and sanitization of mixing equipment used in the manufacturing of dental dosage forms to prevent cross-contamination and ensure product quality and safety.
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Dental Dosage Forms

SOP for Packaging Equipment

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The purpose of this SOP is to provide guidelines for the operation and maintenance of packaging equipment used in the final packaging of dental dosage forms to ensure proper packaging and compliance with regulatory standards.
Click to read the full article.

Dental Dosage Forms

SOP for Labeling Machines

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The purpose of this SOP is to provide guidelines for the operation and maintenance of labeling machines used in the manufacturing of dental dosage forms to ensure accurate labeling and compliance with regulatory standards.
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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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