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SOP Guide for Pharma

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Tag: Ointment batch record SOP

Ointments: SOP for QA Documentation Practices – V 2.0

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SOP for QA Documentation Practices – V 2.0 Procedure for QA Documentation Practices Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/090 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard Operating Procedure…

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Ointments V 2.0

Ointments: SOP for Maintaining GMP Standards – V 2.0

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SOP for Maintaining GMP Standards – V 2.0 Procedure for Maintaining GMP Standards Department Quality Assurance (QA)/Production/Quality Control (QC) SOP No. SOP/Ointment/089 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard Operating Procedure…

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Ointments V 2.0

Ointments: SOP for Approving QC Results – V 2.0

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SOP for Approving QC Results – V 2.0 Procedure for Approving QC Results Department Quality Control (QC)/Quality Assurance (QA) SOP No. SOP/Ointment/088 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard Operating Procedure…

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Ointments V 2.0

Ointments: SOP for Conducting QA Audits in Ointment Manufacturing – V 2.0

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SOP for Conducting QA Audits in Ointment Manufacturing – V 2.0 Procedure for Conducting QA Audits in Ointment Manufacturing Department Quality Assurance (QA)/Compliance SOP No. SOP/Ointment/087 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of…

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Ointments V 2.0

Ointments: SOP for Handling Deviation Reports – V 2.0

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SOP for Handling Deviation Reports – V 2.0 Procedure for Handling Deviation Reports Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/086 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard Operating Procedure…

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Ointments V 2.0

Ointments: SOP for QA Oversight During Packing Operations – V 2.0

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SOP for QA Oversight During Packing Operations – V 2.0 Procedure for QA Oversight During Packing Operations Department Quality Assurance (QA)/Production SOP No. SOP/Ointment/085 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard…

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Ointments V 2.0

Ointments: SOP for Validation of Manufacturing Processes – V 2.0

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SOP for Validation of Manufacturing Processes – V 2.0 Procedure for Validation of Manufacturing Processes Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/084 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard…

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Ointments V 2.0

Ointments: SOP for Batch Manufacturing Record Review – V 2.0

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SOP for Batch Manufacturing Record Review – V 2.0 Procedure for Batch Manufacturing Record Review Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/083 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard…

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Ointments V 2.0

Ointments: SOP for Line Clearance Before Production – V 2.0

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SOP for Line Clearance Before Production – V 2.0 Procedure for Line Clearance Before Production Department Quality Assurance (QA)/Production SOP No. SOP/Ointment/082 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard Operating Procedure…

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Ointments V 2.0

Ointments: SOP for QA Review of Raw Materials – V 2.0

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SOP for QA Review of Raw Materials – V 2.0 Procedure for QA Review of Raw Materials Department Quality Assurance (QA)/Quality Control (QC)/Production SOP No. SOP/Ointment/081 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of…

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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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