Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Bottle Filling Machines

Posted on By

SOP for Bottle Filling Machines

Standard Operating Procedure for Bottle Filling Machines

1) Purpose

The purpose of this SOP is to provide guidelines for the operation and maintenance of bottle filling machines used in the manufacturing of dental dosage forms to ensure accurate and consistent filling of bottles and compliance with regulatory standards.

2) Scope

This SOP applies to all bottle filling machines used in the manufacturing process of dental pastes, gels, and mouthwashes within the pharmaceutical industry.

3) Responsibilities

The Production Department is responsible for operating and cleaning the bottle filling machines. The Quality Assurance (QA) Department is responsible for verifying and documenting compliance with this SOP.

See also  SOP for Environmental Impact Assessment of Equipment

4) Procedure

4.1 Preparation

4.1.1 Verify that the bottle filling machine is clean and in good working condition before use.

4.1.2 Ensure all bottles and caps are prepared and ready for filling according to the batch record.

4.2 Setup and Calibration

4.2.1 Set up the bottle filling machine as per the manufacturer’s instructions and batch record requirements.

4.2.2 Calibrate the bottle filling machine to ensure accurate filling of bottles (volume or weight).

4.2.3 Verify calibration with standard weights or volumes as per the batch record.

4.3 Filling Operation

4.3.1 Start the bottle filling machine and adjust the settings as per the batch record (e.g., fill volume, speed).

See also  SOP for Process Validation of Paste Manufacturing

4.3.2 Place bottles

under the filling nozzles and initiate the filling process.

4.3.3 Monitor the filling process to ensure accurate and consistent filling of bottles.

4.3.4 Record start time, end time, and any deviations observed during filling in the batch record.

4.4 Cap Sealing

4.4.1 After filling, move filled bottles to the cap sealing station according to batch record specifications.

4.4.2 Ensure caps are properly aligned and sealed onto bottles using the cap sealing machine.

4.4.3 Inspect sealed bottles for proper closure and integrity.

4.5 Cleaning

4.5.1 After use, turn off the bottle filling machine and disconnect it from the power source.

See also  SOP for Cross-Contamination Prevention in Equipment Use

4.5.2 Disassemble parts of the bottle filling machine and clean all contact surfaces using approved cleaning agents.

4.5.3 Rinse thoroughly with purified water to remove any residual cleaning agents.

4.5.4 Inspect the bottle filling machine for cleanliness and reassemble it after it is completely dry.

4.6 Maintenance

4.6.1 Perform regular preventive maintenance on the bottle filling machine as per the manufacturer’s guidelines.

4.6.2 Record all maintenance activities in the equipment maintenance log.

5) Abbreviations, if any

QA – Quality Assurance

6) Documents, if any

Batch Record

Equipment Maintenance Log

7) Reference, if any

Current Good Manufacturing Practices (cGMP) guidelines

8) SOP Version

Version 1.0

Dental Dosage Forms Tags:Audit and inspection of dental manufacturing, Calibration of dental equipment, Cleaning validation for dental products, Continuous improvement in dental production, Dental dosage form cleaning procedures, Dental dosage form equipment maintenance, Dental dosage form process validation, Dental Dosage Form SOPs, Dental dosage form validation procedures, Dental dosage forms manufacturing SOPs, Dental gel manufacturing guidelines, Environmental monitoring in dental manufacturing, Equipment qualification for dental dosage forms, Equipment qualification protocols dental, GMP compliance in dental manufacturing, Handling raw materials in dental manufacturing, Mouthwash manufacturing SOP, Packaging of dental products SOP, Quality control in dental dosage forms, Regulatory compliance in dental manufacturing, Risk assessment in dental manufacturing, Safety procedures for dental equipment, SOP for dental dosage form storage, SOP for dental paste production, SOP for dental product labeling, SOP for dental product manufacturing, Stability testing for dental products, Supplier qualification for dental equipment, Training documentation dental industry, Training programs for dental equipment, Validation master plan for dental equipment

Post navigation

Previous Post: Ocular (Eye) Dosage Forms: SOP for Equipment Logbook Maintenance
Next Post: SOP for Material Management and Control

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version