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

Creams: SOP for Documentation of Machine Operations in Cream Production – V 2.0

Posted on By

Creams: SOP for Documentation of Machine Operations in Cream Production – V 2.0

Standard Operating Procedure for Documentation of Machine Operations in Cream Production

Department Creams
SOP No. SOP/CRM/119/2025
Supersedes SOP/CRM/119/2022
Page No. Page 1 of 5
Issue Date 21/01/2026
Effective Date 26/01/2026
Review Date 21/01/2027

1. Purpose

The purpose of this SOP is to define the procedure for documenting machine operations during cream production. Proper documentation ensures compliance with GMP standards, facilitates traceability, and enables quick identification of any deviations or issues during production.

2. Scope

This SOP applies to all machines used in the cream production process, including homogenizers, mixers, filling machines, and other production equipment. It covers the documentation of operational parameters, maintenance activities, and any deviations during production.

3. Responsibilities

  • Production Team: Responsible for documenting machine operation parameters, including speed, temperature, and operational time. They are also responsible for reporting any deviations or equipment issues during production.
  • Quality Control (QC): Responsible for verifying that machine operation documentation is completed accurately and that it complies with GMP standards.
  • Maintenance Team: Responsible for documenting any maintenance or calibration activities performed on production equipment.

4. Accountability

The Production Supervisor is accountable for ensuring that all machine operation parameters are documented correctly. The Maintenance Supervisor is responsible for ensuring that all maintenance activities are documented accurately, and the Quality Control Manager is responsible for reviewing and approving documentation.

See also  Creams: SOP for Scale-Up Studies in Cream Manufacturing - V 2.0

5. Procedure

5.1 Pre-Operation Documentation

  1. Before the start of production, verify that all machines are properly calibrated and in good working condition. Check the equipment manual to ensure that the machine is set to the correct parameters for the current production run.
  2. Document the machine’s ID, the current batch number, and the operator’s name in the Machine Operations Log (Annexure-1).
  3. Record the set parameters, including the desired temperature, speed, and mixing time, as specified in the product’s manufacturing formula or SOP.
  4. Ensure that the machine’s safety features (e.g., emergency stop, alarms) are functioning properly and document these checks in the Machine Safety Check Log (Annexure-2).

5.2 In-Process Documentation

  1. During production, monitor the machine’s performance and record operational parameters at regular intervals. This includes recording the following:
    • Mixing speed (RPM)
    • Temperature
    • Time (e.g., mixing or processing duration)
    • Pressure (if applicable)
  2. Use the Machine Operations Log (Annexure-1) to document the values for each parameter at least every 30 minutes during operation or as per the defined process guidelines.
  3. If the machine is equipped with automated monitoring systems (e.g., sensors or temperature controllers), ensure that these systems are functioning correctly and that the data is recorded automatically.
  4. In the case of any deviation from the established parameters, document the deviation in the Deviation Log (Annexure-3) and notify the Production and QC Managers for investigation.

5.3 Post-Operation Documentation

  1. After the production run is complete, document the final operational parameters in the Machine Operations Log (Annexure-1), including the total operating time and any observed abnormalities.
  2. Record any maintenance performed on the machine during the shift in the Equipment Maintenance Log (Annexure-4). This includes cleaning, repairs, or adjustments made to the machine during production.
  3. Ensure that the equipment is properly shut down, cleaned, and stored according to the manufacturer’s guidelines. Document the shutdown process in the Equipment Shutdown Log (Annexure-5).
See also  Creams: SOP for Water Activity Testing in Creams - V 2.0

5.4 Deviation Handling and Corrective Actions

  1. If any deviations from the specified parameters are observed, stop production immediately and document the issue in the Deviation Log (Annexure-3).
  2. Investigate the cause of the deviation, which may include malfunctioning equipment, incorrect settings, or operator error.
  3. Take corrective actions to resolve the deviation, such as adjusting the machine settings, replacing defective parts, or recalibrating equipment.
  4. Once corrective actions have been taken, document the changes and re-verify that the machine is operating within the specified parameters. Resume production only after ensuring that the issue is fully resolved.

5.5 Documentation Review and Record-Keeping

  1. All documentation related to machine operations must be reviewed and signed off by the Quality Control team to ensure that it complies with GMP standards.
  2. Maintain machine operation logs, deviation logs, maintenance records, and shutdown logs for each batch produced. These records should be stored securely and kept accessible for audits and inspections.
  3. Ensure that records are retained for a minimum of two years or as per regulatory requirements.

6. Abbreviations

  • GMP: Good Manufacturing Practices
  • QC: Quality Control
  • QA: Quality Assurance
  • PPE: Personal Protective Equipment
See also  Creams: SOP for Lubricating Mechanical Parts of Cream-Filling Machines - V 2.0

7. Documents

  1. Annexure-1: Machine Operations Log
  2. Annexure-2: Machine Safety Check Log
  3. Annexure-3: Deviation Log
  4. Annexure-4: Equipment Maintenance Log
  5. Annexure-5: Equipment Shutdown Log

8. References

  • Good Manufacturing Practices (GMP) Guidelines – 21 CFR Part 211
  • International Conference on Harmonisation (ICH) Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • Manufacturer’s Manual for Cream Production Equipment

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Machine Operations Log

Batch Number Machine ID Operator Start Time End Time Operational Parameters
12345 HM-001 John Doe 10:00 AM 2:00 PM Speed: 120 RPM, Temp: 25°C

Annexure-2: Machine Safety Check Log

Machine ID Safety Feature Check Date Pass/Fail Comments
HM-001 Emergency Stop 21/01/2026 Pass All safety features functioning properly

Annexure-3: Deviation Log

Deviation Date Batch Number Deviation Description Corrective Action Taken Operator
21/01/2026 12345 Excessive temperature Adjusted temperature settings John Doe

Annexure-4: Equipment Maintenance Log

Equipment ID Maintenance Date Maintenance Activity Operator Comments
HM-001 21/01/2026 Lubrication Jane Smith Lubricated moving parts

Annexure-5: Equipment Shutdown Log

Machine ID Shutdown Date Reason Operator Comments
HM-001 21/01/2026 End of production John Doe No issues during shutdown

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/03/2024 1.0 Initial Version New SOP Creation QA Head
01/03/2025 2.0 Format Revision and Updates Standardization of Document QA Head
Creams V 2.0 Tags:Batch record documentation for creams, Change control procedures for cream manufacturing, Cleaning and sanitization SOPs in creams production, Complaint handling SOPs in creams production, Continuous improvement SOPs for cream manufacturing, Cream manufacturing process guidelines, Creams production documentation practices, Deviation handling SOPs in creams production, Employee training SOPs in creams manufacturing, Environmental monitoring SOPs in creams manufacturing, Equipment calibration SOPs for cream manufacturing, GMP compliance in creams production, Internal audit procedures in creams production, Packaging and labeling SOPs for creams, Pharmaceutical SOPs, Product quality review procedures for creams, Product release criteria SOPs for creams, Quality control SOPs for creams, ream manufacturing SOP, Regulatory requirements for cream production SOPs, Risk management SOPs in creams manufacturing, Stability testing SOPs for cream products, Standard operating procedures for skincare products, Supplier qualification SOPs for cream ingredients, Validation protocols for cream production processes

Post navigation

Previous Post: BA-BE Studies: SOP for IMP Destruction or Return Process – V 2.0
Next Post: API Manufacturing: SOP for Emergency Handling in Solvent Area – V 2.0

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
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams 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