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API Manufacturing: SOP for Use of Fluid Bed Dryers in API Processing – V 2.0

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API Manufacturing: SOP for Use of Fluid Bed Dryers in API Processing – V 2.0

Standard Operating Procedure for Use of Fluid Bed Dryers in API Processing

Department API Manufacturing
SOP No. SOP/API/071/2025
Supersedes SOP/API/071/2022
Page No. Page 1 of 10
Issue Date 13/04/2025
Effective Date 15/04/2025
Review Date 13/04/2026

1. Purpose

To define the procedure for the use of fluid bed dryers (FBD) in the drying of APIs and intermediates, ensuring efficient moisture reduction, uniform drying, and adherence to cGMP requirements.

2. Scope

This SOP applies to all drying operations using fluid bed dryers in the API manufacturing unit, including equipment preparation, operation, monitoring, unloading, and cleaning.

3. Responsibilities

  • Production Operator: Operate the FBD as per process parameters and ensure safety during use.
  • Production Supervisor: Review dryer setup, monitor process, and verify completion of documentation.
  • QA Department: Ensure compliance with SOP, perform line clearance, and review batch records.
  • Engineering Department: Maintain FBD and associated utilities and perform preventive maintenance.
See also  API Manufacturing: SOP for TLC Plate Preparation and Result Interpretation - V 2.0

4. Accountability

The Production Head is accountable for execution of drying using the FBD. QA Head is responsible for final approval and regulatory compliance review.

5. Procedure

5.1 Pre-Operation Checks

  1. Ensure FBD is cleaned and labeled “Cleaned”.
  2. Verify calibration status of inlet and exhaust temperature sensors, differential pressure gauges, and control panels.
  3. Check integrity of FBD filter bags and record observations in the checklist.
  4. Review line clearance from QA before loading the batch.

5.2 Charging Material into FBD

  1. Transfer material from containers to the FBD bowl using a closed transfer system or under LAF.
  2. Note the batch number, product name, weight of wet material, and date in the drying logbook.
  3. Securely attach the bowl to the FBD column and ensure proper gasket sealing.
See also  API Manufacturing: SOP for Moisture Content Analysis by LOD - V 2.0

5.3 Drying Operation

  1. Set the following parameters as per BMR:
    • Inlet temperature (e.g., 60–80°C)
    • Drying time (e.g., 20–40 minutes)
    • Fluidization air velocity
    • Target LOD or moisture level
  2. Start blower to initiate fluidization.
  3. Turn on heaters and monitor drying cycle in the PLC (if automated) or manually.
  4. Record temperature, time, and airflow every 10–15 minutes in “FBD Operation Log” (Annexure-1).
  5. Stop heating once in-process LOD result is within limits.

5.4 Unloading and Post-Drying Steps

  1. Allow cooling of the material before unloading.
  2. Discharge dry API into clean, labeled containers or drums lined with polybags.
  3. Label each drum with:
    • Product Name
    • Batch No.
    • Net Weight
    • Drying Date
  4. Send final sample to QC for testing and retain samples as per retention policy.

5.5 Cleaning and Maintenance

  1. Clean product contact parts with suitable cleaning agent as per cleaning SOP.
  2. Dry and inspect before labeling “Cleaned”.
  3. Record cleaning in equipment cleaning logbook.
  4. Engineering team shall perform periodic inspection and preventive maintenance.

See also  API Manufacturing: SOP for Raw Material Sampling Procedure - V 2.0

6. Abbreviations

  • FBD: Fluid Bed Dryer
  • LOD: Loss on Drying
  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • QC: Quality Control
  • BMR: Batch Manufacturing Record

7. Documents

  1. FBD Operation Log (Annexure-1)
  2. Cleaning Logbook
  3. Batch Manufacturing Record

8. References

  • ICH Q7 – GMP for Active Pharmaceutical Ingredients
  • Internal Equipment Operation Manual
  • US FDA 21 CFR Part 211

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: FBD Operation Log

Date Batch No. Start Time End Time Inlet Temp (°C) LOD (%) Operator
13/04/2025 API-FBD-20250413 09:15 09:50 70 0.35

Revision History:

Revision Date Revision No. Details Reason Approved By
01/01/2022 1.0 Initial SOP Release New Equipment Qualification QA Head
13/04/2025 2.0 Added Inlet/Exhaust Monitoring and Validation Parameters Process Optimization QA Head
API Manufacturing V 2.0 Tags:API batch record, API BMR, API calibration, API centrifuge, API cleaning, API crystallization, API deviation, API documentation, API drying, API equipment cleaning, API filtration, API GMP compliance, API granulation, API hold time, API impurities, API line clearance, API manufacturing, API process, API quality control, API reactor, API sampling, API solvent handling, API validation, API waste disposal, API yield

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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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