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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Pharmaceutical SOPs

Creams: SOP for Handling Excipient Dispensing in Cream Formulations – V 2.0

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Creams: SOP for Handling Excipient Dispensing in Cream Formulations – V 2.0 Standard Operating Procedure for Handling Excipient Dispensing in Cream Formulations Department Creams SOP No. SOP/CRM/005/2025 Supersedes SOP/CRM/005/2022 Page No. Page 1 of 6 Issue Date 20/03/2025 Effective Date 25/03/2025 Review Date 20/03/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is…

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Creams V 2.0

Creams: SOP for Handling and Storage of Active Pharmaceutical Ingredients (APIs) for Creams – V 2.0

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Creams: SOP for Handling and Storage of Active Pharmaceutical Ingredients (APIs) for Creams – V 2.0 Standard Operating Procedure for Handling and Storage of Active Pharmaceutical Ingredients (APIs) for Creams Department Creams SOP No. SOP/CRM/004/2025 Supersedes SOP/CRM/004/2022 Page No. Page 1 of 7 Issue Date 15/03/2025 Effective Date 20/03/2025 Review Date 15/03/2026 1. Purpose The…

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Creams V 2.0

Creams: SOP for Cross-Verification of Weighed Materials – V 2.0

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Creams: SOP for Cross-Verification of Weighed Materials – V 2.0 Standard Operating Procedure for Cross-Verification of Weighed Materials Department Creams SOP No. SOP/CRM/003/2025 Supersedes SOP/CRM/003/2022 Page No. Page 1 of 6 Issue Date 10/03/2025 Effective Date 15/03/2025 Review Date 10/03/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish a procedure…

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Creams V 2.0

Creams: SOP for Dispensing Raw Materials for Cream Formulations – V 2.0

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Creams: SOP for Dispensing Raw Materials for Cream Formulations – V 2.0 Standard Operating Procedure for Dispensing Raw Materials for Cream Formulations Department Creams SOP No. SOP/CRM/002/2025 Supersedes SOP/CRM/002/2022 Page No. Page 1 of 8 Issue Date 05/03/2025 Effective Date 10/03/2025 Review Date 05/03/2026 1. Purpose The purpose of this Standard Operating Procedure (SOP) is…

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Creams V 2.0

Creams: SOP for Material Identification and Labeling in Cream Manufacturing – V 2.0

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Creams: SOP for Material Identification and Labeling in Cream Manufacturing – V 2.0 Standard Operating Procedure for Material Identification and Labeling in Cream Manufacturing Department Creams SOP No. SOP/CRM/001/2025 Supersedes SOP/CRM/001/2022 Page No. Page 1 of 8 Issue Date 01/03/2025 Effective Date 05/03/2025 Review Date 01/03/2026 1. Purpose The purpose of this Standard Operating Procedure…

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Creams V 2.0

How do SOP’s contribute to the documentation and investigation of quality incidents or deviations in pharmaceutical manufacturing?

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Contribution of SOP’s to Documentation and Investigation of Quality Incidents or Deviations in Pharmaceutical Manufacturing Standard Operating Procedures (SOP’s) play a crucial role in documenting and investigating quality incidents or deviations in pharmaceutical manufacturing to ensure product quality, safety, and compliance. Here’s how SOP’s contribute to this process: 1. Incident Reporting Procedures SOP’s establish clear…

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SOP - FAQs

What role do SOP’s play in the validation and control of analytical methods used for product testing in pharmaceutical laboratories?

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Role of SOP’s in Validation and Control of Analytical Methods in Pharmaceutical Laboratories Standard Operating Procedures (SOP’s) play a crucial role in ensuring the accuracy, reliability, and compliance of analytical methods used for product testing in pharmaceutical laboratories. Here’s how SOP’s contribute to the validation and control of analytical methods: 1. Method Development and Validation…

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SOP - FAQs

How are SOP’s used to establish and maintain a state of inspection readiness in pharmaceutical manufacturing facilities?

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Establishing and Maintaining Inspection Readiness in Facilities through SOP’s Standard Operating Procedures (SOP’s) play a critical role in ensuring that pharmaceutical manufacturing facilities are prepared for inspections by regulatory agencies. Inspection readiness involves implementing proactive measures to demonstrate compliance with regulatory requirements and quality standards. Here’s how SOP’s are used to establish and maintain a…

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SOP - FAQs

Can you discuss the role of SOP’s in ensuring the proper handling and disposal of controlled substances in pharmaceutical operations?

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Role of SOP’s in Handling and Disposal of Controlled Substances Standard Operating Procedures (SOP’s) play a crucial role in ensuring the proper handling and disposal of controlled substances in pharmaceutical operations to prevent diversion, misuse, and environmental contamination. Here’s how SOP’s contribute to this process: 1. Receipt and Storage Procedures SOP’s establish protocols for the…

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SOP - FAQs

Can you provide examples of how SOP’s are adapted to accommodate technological advancements and innovations in pharmaceutical production?

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Adapting SOP’s to Accommodate Technological Advancements and Innovations Standard Operating Procedures (SOP’s) play a crucial role in ensuring consistency, quality, and compliance in pharmaceutical production. As technological advancements and innovations continue to transform the pharmaceutical industry, SOP’s must be adapted to leverage these advancements effectively. Here are examples of how SOP’s are adapted to accommodate…

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SOP - FAQs

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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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