Kajian Risiko Validasi Pembersihan Mesin yang Dilakukan Secara Manual Dengan Metode Failure Mode and Effects Analysis
Abstrak
Kontaminasi silang pada sarana produksi adalah hal yang sangat dihindari sehingga perlu dilakukannya pembersihan yang sudah divalidasi karena residu yang tersisa dapat menjadi cemaran. Namun, terdapat risiko yang dapat terjadi selama dilakukannya validasi pembersihan. Oleh karena itu penting untuk mengkaji risiko tersebut. Penelitian ini akan mengkaji resiko yang dapat terjadi pada setiap tahapan validasi pembersihan dengan metode Failure Mode and Effects Analysis (FMEA). Penelitian dilakukan dengan cara observasional dan wawancara langsung di salah satu industri farmasi di Kota Bandung. Tahapan kajian risiko dimulai dengan mengidentifikasi risiko, menganalisis risiko berdasarkan tingkat keparahan, memberikan skor sehingga didapatkan nilai RPN, serta mengevaluasi risiko. Dari hasil kajian risiko, didapatkan sebanyak 26 risiko dengan 16 risiko minor, 4 risiko moderat dan 6 risiko mayor. Risiko yang termasuk dalam kategori mayor dibuat tindakan pengendalian risiko untuk mengurangi risiko terjadinya kegagalan dalam validasi pembersihan. Industri farmasi dapat melakukan tindakan pencegahan dan pengendalian dari hasil kajian risiko ini seperti pengecekan terhadap sarana penunjang kritis yang ada, penentuan marker, pelaksanaan proses validasi, serta mempertimbangkan untuk pembersihan secara otomatis.
Kata Kunci
Teks Lengkap:
PDFReferensi
Ferro Uriguen A, Beobide Telleria I, Martínez Arrechea S, Miró Isasi B, Sampedro Yangüela C, Urretavizcaya Anton M. Determination of the cross-contamination and validation of the cleaning process for an automated personalised dosing system. Eur J Hosp Pharm. 2022 May;29(3):157–63.
Tanyous JN. Cleaning Validation: Complete Guide for Health - Based Approach in Chemical Cross - Contamination Risk Assessment. PDA Journal of Pharmaceutical Science and Technology. 2019;73(2):204–10.
Spoerk M, Koutsamanis I, Matić J, Eder S, Patricia Alva Zúñiga C, Poms J, et al. Novel Cleaning-in-Place Strategies for Pharmaceutical Hot Melt Extrusion. Pharmaceutics. 2020 June 24;12(6):588.
Pant KJ, Cotter PD, Wilkinson MG, Sheehan JJ. Towards sustainable Cleaning‐in‐Place (CIP) in dairy processing: Exploring enzyme‐based approaches to cleaning in the Cheese industry. Comp Rev Food Sci Food Safe. 2023 Sept;22(5):3602–19.
Coelho AS, Arribada RG, Lages EB. Cleaning Validation for Residual Estimation of Mometasone Furoate on Stainless-Steel Surface of Pharmaceutical Manufacturing Equipment Using a UHPLC-UV Method. PDA Journal of Pharmaceutical Science and Technology. 2020;74(1):41–8.
Bambang Gunawan RM. The Role Of Risk Management In Enhancing Company Resilience. Eduvest. 2024 May 25;4(5):4151–9.
Pascarella G, Rossi M, Montella E, Capasso A, De Feo G, Botti G, et al. Risk Analysis in Healthcare Organizations: Methodological Framework and Critical Variables. RMHP. 2021 July;Volume 14:2897–911.
ICH. Quality Risk Management Q9. ICH Harmonised Tripartite Guideline; 2005.
BPOM. Peraturan BPOM No. 7 Tahun 2024 tentang Cara Pembuatan Obat yang Baik. BPK RI; 2024.
El-Awady SMM. Overview of Failure Mode and Effects Analysis (FMEA): A Patient Safety Tool. Global Journal on Quality and Safety in Healthcare. 2023 Feb 1;6(1):24–6.
Van Der Galiën R, Langen AL, Jacobs LJM, Hagen B, Flahive K, Chatterjee SD, et al. Setup of a Contamination Control Strategy Using the Hazard Analysis Critical Control Point (HACCP) Methodology. PDA Journal of Pharmaceutical Science and Technology. 2023;77(4):317–28.
Valavala S, Seelam N, Tondepu S, Sundaramurthy V. Cleaning Method Validation for Estimation of Dipyridamole Residue on the Surface of Drug Product Manufacturing Equipment Using Swab Sampling and by High Performance Liquid Chromatographic Technique. tjps. 2020 Apr 1;17(2):182–9.
APIC. Guidance on Aspect Of Cleaning Validation in Active Pharmaceutical Ingredient Plants. Active Pharmaceutical Ingredients Committee; 2021.
Singh K, Tamta B, Mukopadayay S. Cleaning validation process in pharmaceutical industry: A review. ijhs. 2022 June 7;13557–73.
McGowan J, Wojahn A, Nicolini JR. Risk Management Event Evaluation and Responsibilities. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 [cited 2025 Oct 13]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK559326/
Moura MJ, Pereira AD, Santos DJF, Silva AG, Paiva CCAD, Duarte BPM. Cleaning validation in pharmaceutical quality control laboratories: a structured protocol for contamination risk mitigation. DARU J Pharm Sci. 2025 July 3;33(2):20.
Röcker R, Eggers B, Kramer A, Stope MB. Effective manual cleaning as the first step of reprocessing glass probes of a medical device for non-invasive physical plasma therapy. GMS Hygiene and Infection Control [Internet]. 2024 [cited 2025 Oct 14];19. Available from: https://journals.publisso.de/en/journals/hic/volume19/dgkh000486
Benčina M, Rawat N, Paul D, Kovač J, Iglič A, Junkar I. Surface Modification of Stainless Steel for Enhanced Antibacterial Activity. ACS Omega. 2025 Apr 8;10(13):13361–9.
Tune Tibesso D, Gabriel T, Balcha Balla T, Belete A. Compliance of Pharmaceutical Manufacturing Companies to Good Manufacturing Practices in Heating, Ventilation, and Air‐Conditioning Systems: The Case of Local Ethiopian Firms. Natalini B, editor. Advances in Pharmacological and Pharmaceutical Sciences. 2024 Jan;2024(1):6109415.
Dhandapani K, Kella A, Narayanasamy D. Maintaining a Sterile Environment: Validation and Qualification Strategies for Heating, Ventilation, and Air Conditioning Systems Adhering to Current Good Manufacturing Practices in Pharmaceutical Facilities. Cureus [Internet]. 2024 Sept 1 [cited 2025 Oct 13]; Available from: https://www.cureus.com/articles/279435-maintaining-a-sterile-environment-validation-and-qualification-strategies-for-heating-ventilation-and-air-conditioning-systems-adhering-to-current-good-manufacturing-practices-in-pharmaceutical-facilities
Patera J, Štípková G, Zámostný P, Bělohlav Z, Vltavský Z. Effect of dirty-hold time on cleaning process of pharmaceutical equipment. Pharmaceutical Development and Technology. 2013 Feb;18(1):274–9.
Refbacks
- Saat ini tidak ada refbacks.











