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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Elixers V 2.0

Elixir Department: SOP for Double Check System During Material Dispensing – V 2.0

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This SOP establishes the procedure for implementing a Double Check System during the dispensing of raw materials, excipients, and solvents in the Elixir Department. It ensures that dispensing is carried out with full accuracy, traceability, and regulatory compliance, reducing the risk of human error.
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Elixers V 2.0

Elixir Department: SOP for Handling Material Return Post Dispensing – V 2.0

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This SOP outlines the procedure for managing returned materials after partial dispensing during elixir manufacturing. It ensures proper handling, identification, storage, and documentation of returned raw materials to maintain their quality and traceability.
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Elixers V 2.0

Elixir Department: SOP for Handling Damaged Raw Material Packs – V 2.0

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The purpose of this SOP is to establish a standard procedure for identifying, reporting, and managing damaged raw material containers or packs received in the Elixir Department, ensuring product integrity, compliance, and traceability.
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Elixers V 2.0

Elixir Department: SOP for Segregation of Quarantined and Approved Materials – V 2.0

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This SOP outlines the procedure for physical and systemic segregation of quarantined and approved raw materials to avoid cross-contamination, mix-ups, and ensure compliance with GMP regulations within the Elixir Department.
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Elixers V 2.0

Elixir Department: SOP for Calibration of Dispensing Balances – V 2.0

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To define a systematic procedure for the calibration of balances used during the dispensing of raw materials and excipients in the Elixir Department. This ensures weighing accuracy, minimizes errors, and maintains compliance with GMP.
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Elixers V 2.0

Elixir Department: SOP for Use of Barcode Systems During Dispensing – V 2.0

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This SOP defines the procedure for the use of barcode scanning systems during the dispensing of raw materials and excipients in the Elixir Department to ensure accuracy, traceability, and compliance with Good Manufacturing Practices (GMP).
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Elixers V 2.0

Elixir Department: SOP for Dispensing Under Laminar Airflow Cabinet – V 2.0

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The purpose of this SOP is to define the standardized procedure for dispensing raw materials and excipients under a laminar airflow (LAF) cabinet to maintain cleanliness, prevent contamination, and ensure compliance with GMP in the Elixir Department.
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Elixers V 2.0

Elixir Department: SOP for Controlled Substance Dispensing for Elixirs – V 2.0

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This SOP outlines the standardized procedure for secure, accurate, and regulatory-compliant dispensing of controlled substances used in elixir formulations. It ensures traceability, minimizes risks of misuse, and aligns with national regulatory requirements.
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Elixers V 2.0

Elixir Department: SOP for Dispensing Solvents and Vehicles – V 2.0

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To define a standard method for safe, accurate, and contamination-free dispensing of solvents and vehicles used in the manufacturing of oral liquid elixirs, ensuring consistency, traceability, and compliance with cGMP and regulatory guidelines.
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Elixers V 2.0

Elixir Department: SOP for Dispensing Excipients for Oral Liquid Formulations – V 2.0

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The purpose of this SOP is to describe the procedure for accurate and contamination-free dispensing of excipients used in oral liquid elixir formulations. The procedure ensures consistency, traceability, and regulatory compliance throughout the dispensing process.
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Elixers 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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