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

Biosimilars: SOP for Colony Screening and Expression Analysis – V 2.0

Posted on By


Biosimilars: SOP for Colony Screening and Expression Analysis – V 2.0


Standard Operating Procedure for Colony Screening and Expression Analysis in Biosimilar Cell Line Development

Department Biosimilars
SOP No. SOP/BS/012/2025
Supersedes SOP/BS/012/2022
Page No. Page 1 of 13
Issue Date 04/05/2025
Effective Date 06/05/2025
Review Date 04/05/2026

1. Purpose

To define the standardized method for colony screening and initial expression analysis in transfected cell lines to identify and select high-producing biosimilar clones.

2. Scope

This SOP applies to R&D personnel involved in screening colonies derived from stable or transient transfection experiments during biosimilar cell line development.

3. Responsibilities

  • Research Scientist: Designs screening strategy and conducts expression assays.
  • Lab Technician: Maintains colonies and performs ELISA/western blot sample prep.
  • QA Personnel: Ensures documentation of screening records and result traceability.
See also  Biosimilars: SOP for Limiting Dilution Cloning - V 2.0

4. Accountability

The Head of Cell Line Development is accountable for ensuring that colony screening procedures are followed as per regulatory and experimental standards.

5. Procedure

5.1 Colony Observation and Selection

  1. Observe colonies in 96-well plates under an inverted microscope.
  2. Score colonies based on morphology, growth rate, and adherence (if adherent cells).
  3. Mark colonies with good morphology and transfer to 24-well plates for further expansion.

5.2 Expansion and Media Collection

  1. Grow selected colonies in complete growth medium in 24-well plates for 3–5 days.
  2. Harvest supernatant (if secreted protein) or collect cell lysate (if intracellular protein).
  3. Store samples at -20°C until analyzed.

5.3 Expression Analysis

  1. Perform preliminary expression analysis using:
    • ELISA – for quantification of secreted protein
    • SDS-PAGE – for molecular weight estimation
    • Western Blot – for identity confirmation (if needed)
  2. Document results in the Expression Screening Log (Annexure-1).
See also  Biosimilars: SOP for Stable Cell Line Development - V 2.0

5.4 Selection Criteria

  1. Select top 10–20% colonies showing highest expression levels and acceptable growth morphology.
  2. Expand into 6-well plates or T-25 flasks and maintain with consistent passage records.

5.5 Data Review and Record Keeping

  1. Review data with QA and assign Clone ID to selected colonies.
  2. Update all records including source plate, expression level, and passage status in Clone Screening Summary Sheet (Annexure-2).

6. Abbreviations

  • SOP: Standard Operating Procedure
  • ELISA: Enzyme-Linked Immunosorbent Assay
  • SDS-PAGE: Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis
  • QA: Quality Assurance

7. Documents

  1. Expression Screening Log (Annexure-1)
  2. Clone Screening Summary Sheet (Annexure-2)
See also  Biosimilars: SOP for Vector Design and Cloning - V 2.0

8. References

  • ICH Q5D – Cell Substrates
  • WHO Guidelines on Recombinant Protein Production
  • CDSCO Technical Manual for Biologics

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Expression Screening Log

Date Plate ID Well No. Clone ID Assay Type Result Selected
03/05/2025 EX-01 D8 CL-BS-012 ELISA 72 ng/mL Yes

Annexure-2: Clone Screening Summary Sheet

Clone ID Source Plate Expression (ng/mL) Assay Type Selected For Expansion Remarks
CL-BS-012 EX-01:D8 72 ELISA Yes Top 5%

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
04/05/2025 2.0 Added new selection criteria and expanded annexures Annual review
Biosimilars V 2.0 Tags:biosimilar manufacturing SOP, biosimilar process validation SOP, biosimilar quality control procedure, cell line development SOP biosimilars, chromatography SOP biosimilars, cleaning validation SOP for biosimilar equipment, cleanroom SOP for biologics manufacturing, deviation handling SOP in bioprocess, downstream processing SOP, environmental monitoring SOP biosimilars, GMP SOP for biosimilars, host cell protein removal SOP, inline UV monitoring SOP biosimilars, media preparation SOP for biosimilars, protein purification SOP, purification skid calibration SOP, SOP for bioreactor inoculation biosimilars, SOP for biosimilar cell banking, SOP for cell culture in biosimilar production, SOP for chromatography column packing, SOP for ELISA-based clone screening, SOP for endotoxin testing in biologics, SOP for filter sterilization in downstream processing, SOP for glycosylation analysis in biosimilars, SOP for master cell bank, SOP for protein A chromatography steps, SOP for resin qualification in biosimilar purification, SOP for viral clearance in biosimilar production, SOP for working cell bank, upstream processing SOP biosimilars

Post navigation

Previous Post: API Manufacturing: SOP for Line Clearance Before Start of Manufacturing – V 2.0
Next Post: BA-BE Studies: SOP for Periodic Clinical Safety Assessments – 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