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SOP Guide for Pharma

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Revised SOPs for Ointments V 2.0

Ointments: SOP for Handling Hazardous Materials During Dispensing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish a safe and standardized process for handling hazardous raw materials during dispensing in ointment manufacturing. This ensures the safety of personnel, prevents contamination, and maintains compliance with Good Manufacturing Practices (GMP) and occupational health standards.
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Ointments V 2.0

Ointments: SOP for Cleaning of Dispensing Booths – V 2.0

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This Standard Operating Procedure (SOP) outlines the process for cleaning dispensing booths used in the weighing and dispensing of raw materials for ointment manufacturing. The objective is to prevent cross-contamination, maintain a controlled environment, and ensure compliance with Good Manufacturing Practices (GMP).
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Ointments V 2.0

Ointments: SOP for Cross-Contamination Prevention During Dispensing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to define procedures for preventing cross-contamination during the dispensing of raw materials for ointment manufacturing. This ensures product integrity, compliance with Good Manufacturing Practices (GMP), and patient safety.
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Ointments V 2.0

Ointments: SOP for Maintaining Traceability of Dispensed Materials – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish a system for maintaining the traceability of dispensed materials used in ointment manufacturing. This ensures compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal quality control standards.
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Ointments V 2.0

Ointments: SOP for Handling and Labeling Dispensed Materials – V 2.0

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This Standard Operating Procedure (SOP) provides guidelines for the proper handling and labeling of dispensed raw materials in ointment manufacturing. The objective is to prevent contamination, ensure traceability, and maintain compliance with Good Manufacturing Practices (GMP).
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Ointments V 2.0

Ointments: SOP for Weighing of Raw Materials for Ointment Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for accurately weighing raw materials for ointment manufacturing. This ensures compliance with Good Manufacturing Practices (GMP), maintains batch consistency, and prevents cross-contamination.
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Ointments V 2.0

Ointments: SOP for Verification of Raw Materials Before Dispensing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to ensure that all raw materials are properly verified before dispensing for ointment manufacturing. This verification process guarantees compliance with Good Manufacturing Practices (GMP) and prevents errors, contamination, or the use of incorrect materials in production.
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Ointments V 2.0

Ointments: SOP for Raw Material Storage in Designated Areas – V 2.0

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This Standard Operating Procedure (SOP) outlines the proper storage of raw materials used in ointment manufacturing. The objective is to ensure materials are stored in compliance with Good Manufacturing Practices (GMP) to maintain their integrity, prevent contamination, and facilitate traceability.
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Ointments V 2.0

Ointments: SOP for Receiving Raw Materials in Ointment Manufacturing – V 2.0

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The purpose of this Standard Operating Procedure (SOP) is to establish a consistent process for receiving raw materials used in ointment manufacturing. This procedure ensures compliance with Good Manufacturing Practices (GMP), prevents contamination, and maintains material integrity.
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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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