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SOP Guide for Pharma

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Revised SOPs for Ointments V 2.0

Ointments: SOP for Conducting Preventive Maintenance on Validated Equipment – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting preventive maintenance on validated equipment used in ointment manufacturing. Proper maintenance ensures continued operational efficiency, reliability, and compliance with regulatory standards.
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Ointments V 2.0

Ointments: SOP for Handling Equipment Validation Failures – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define a systematic approach for identifying, investigating, and resolving equipment validation failures in ointment manufacturing. Proper handling of validation failures ensures compliance with regulatory standards and prevents deviations in product quality.
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Ointments V 2.0

Ointments: SOP for Validation of Automated Equipment – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for validating automated equipment used in ointment manufacturing. This ensures that automated systems perform as intended and meet regulatory compliance requirements.
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Ointments V 2.0

Ointments: SOP for Ensuring Calibration of Critical Instruments – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish a systematic approach for ensuring the calibration of critical instruments used in ointment manufacturing. Proper calibration ensures measurement accuracy, consistency, and compliance with regulatory standards.
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Ointments V 2.0

Ointments: SOP for Documentation of Equipment Validation – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for documenting equipment validation activities in ointment manufacturing. Proper documentation ensures compliance with regulatory requirements, traceability, and verification of validation processes.
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Ointments V 2.0

Ointments: SOP for Requalification of Key Equipment – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for requalification of key equipment in ointment manufacturing. Requalification ensures that critical equipment continues to perform within established specifications and regulatory requirements over time.
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Ointments V 2.0

Ointments: SOP for Performance Qualification (PQ) of Filling Machines – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Performance Qualification (PQ) of filling machines used in ointment manufacturing. This ensures that the machines consistently operate within specified parameters and meet quality and regulatory requirements.
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Ointments V 2.0

Ointments: SOP for Operational Qualification (OQ) of Mixing Tanks – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Operational Qualification (OQ) of mixing tanks in ointment manufacturing. This ensures that the mixing tanks operate consistently and reliably within specified parameters under normal operating conditions.
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Ointments V 2.0

Ointments: SOP for Installation Qualification (IQ) of Equipment – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Installation Qualification (IQ) of new, modified, or relocated equipment in ointment manufacturing. This ensures that all installed equipment complies with predefined specifications and regulatory requirements.
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Ointments V 2.0

Ointments: SOP for Equipment Qualification in Ointment Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define the process for equipment qualification in ointment manufacturing. This ensures that all equipment used in production meets predefined operational, performance, and compliance requirements before use.
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Ointments V 2.0

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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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