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SOP for Weighing and Dispensing of Raw Materials

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SOP for Weighing and Dispensing of Raw Materials

Standard Operating Procedure for Weighing and Dispensing of Raw Materials

1) Purpose

The purpose of this SOP is to ensure the accurate weighing and dispensing of raw materials used in the manufacturing of dental dosage forms to maintain product quality and consistency.

2) Scope

This SOP applies to all raw materials used in the manufacturing of dental pastes, gels, and mouthwashes within the pharmaceutical industry.

3) Responsibilities

The Production Department is responsible for the accurate weighing and dispensing of raw materials. The Quality Assurance (QA) Department is responsible for verifying and documenting the weighing and dispensing process.

See also  SOP for Equipment Decommissioning

4) Procedure

4.1 Preparation

4.1.1 Verify the identity and quality of raw materials before weighing and dispensing.

4.1.2 Ensure the weighing scales are calibrated and in good working condition.

4.1.3 Gather all necessary equipment, such as weighing scales, containers, and personal protective equipment (PPE).

4.2 Weighing

4.2.1 Place the container on the weighing scale and tare the scale to zero.

4.2.2 Carefully weigh the required quantity of raw material according to the batch record.

4.2.3 Record the weight of the material in the batch record and on the container label.

4.3 Dispensing

4.3.1 Transfer the weighed material to the designated production area using appropriate handling techniques.

See also  SOP for Emergency Procedures for Equipment Failure

4.3.2 Ensure that the material is dispensed into the correct production batch as per the batch record.

4.3.3 Label the container with the material name, batch number, and weight.

4.4 Documentation

4.4.1 Document all weighing and dispensing activities in the batch record.

4.4.2 Attach any relevant data, such as weighing scale printouts, to the batch record.

4.5 Approval

4.5.1 Submit the completed batch record to the QA Department for review and approval.

4.5.2 Store the approved batch record in the production documentation file.

5) Abbreviations, if any

PPE – Personal Protective Equipment

6) Documents, if any

Batch Record

Weighing Scale Calibration Records

See also  SOP for GMP Compliance in Equipment Handling

7) Reference, if any

Current Good Manufacturing Practices (cGMP) guidelines

8) SOP Version

Version 1.0

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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

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