Six Sigma: Process of Understanding the Control and Capability of Ranitidine Hydrochloride Tablet
2011

Improving Ranitidine Hydrochloride Tablet Production with Six Sigma

Sample size: 40 publication Evidence: high

Author Information

Author(s): Chabukswar AR, Jagdale SC, Kuchekar BS, Joshi VD, Deshmukh GR, Kothawade HS, Kuckekar AB, Lokhande PD

Primary Institution: MAEER’s Maharashtra Institute of Pharmacy

Hypothesis

The study aims to achieve perfection in tablet manufacturing by improving the current manufacturing process of Ranitidine hydrochloride tablets.

Conclusion

The application of Six Sigma led to significant improvements in process capability, yield, and overall efficiency in the production of Ranitidine hydrochloride tablets.

Supporting Evidence

  • The sigma level of the manufacturing process improved from 1.5 to 4.
  • Rework was reduced by 50%.
  • Overall efficiency improved by approximately 30%.
  • Cost reduction of approximately Rs.90 to 95 lakhs per annum was achieved.

Takeaway

This study shows how using a special method called Six Sigma can help make better quality medicine by reducing mistakes in making tablets.

Methodology

The study used the DMAIC methodology of Six Sigma, which includes defining goals, measuring current processes, analyzing data, improving processes, and controlling outcomes.

Digital Object Identifier (DOI)

10.4103/0975-1483.76415

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