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SOP for Automated Drop Filling Machine

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SOP for Automated Drop Filling Machine

Standard Operating Procedure for Automated Drop Filling Machine

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the Automated Drop Filling Machine used in the pharmaceutical manufacturing of otic dosage forms to ensure accurate and consistent filling of drops into containers.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of the Automated Drop Filling Machine in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the Automated Drop Filling Machine as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring and verifying the accuracy of drop filling.
Maintenance Personnel: Responsible for maintaining the Automated Drop Filling Machine in proper working condition.

See also  SOP for Change Control Management

4) Procedure

4.1 Pre-operation Checks
4.1.1 Inspection
4.1.1.1 Inspect the Automated Drop Filling Machine for cleanliness and integrity before use.
4.1.1.2 Ensure that all nozzles, valves, and conveyor belts are clean and free from residue.
4.1.1.3 Verify that the machine is calibrated and operating within specified parameters.

4.1.2 Preparation
4.1.2.1 Clean and sanitize the filling machine and the surrounding area.
4.1.2.2 Check and prepare drop containers and lids for filling.
4.1.2.3 Ensure that the machine is primed and ready for operation according to manufacturer’s instructions.

4.2 Operation
4.2.1 Filling Process
4.2.1.1 Power on the Automated Drop Filling Machine and set the filling parameters.
4.2.1.2 Load containers onto the conveyor belt and position them for filling.
4.2.1.3 Initiate the filling process, ensuring that all containers are filled accurately and consistently with drops.

See also  SOP for Reverse Osmosis Unit

4.2.2 Safety Precautions
4.2.2.1 Wear appropriate PPE, including gloves and lab coat, when handling drop filling operations.
4.2.2.2 Ensure that all machine guards and safety interlocks are in place and functional.
4.2.2.3 Monitor the filling process closely to detect any anomalies or deviations from the set parameters.

4.3 Post-operation
4.3.1 Shutdown
4.3.1.1 Complete the filling process and remove all containers from the machine.
4.3.1.2 Clean and sanitize the filling machine and conveyor belts according to approved procedures.
4.3.1.3 Perform post-operation checks to ensure no residual product or contamination issues.

4.3.2 Maintenance
4.3.2.1 Regularly inspect and clean all parts of the Automated Drop Filling Machine.
4.3.2.2 Lubricate moving parts as per manufacturer’s recommendations.
4.3.2.3 Keep maintenance records and document any issues or repairs performed.

See also  SOP for Compounder

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure
PPE: Personal Protective Equipment

6) Documents, if any

Maintenance records
Filling logs for the Automated Drop Filling Machine
Calibration records for the machine

7) Reference, if any

Manufacturer’s manual for the Automated Drop Filling Machine
Pharmacopeial guidelines for pharmaceutical manufacturing processes

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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