We are pleased to share that ARG Academy successfully conducted a ๐ฑ-๐ฑ๐ฎ๐ ๐ถ๐ป-๐ต๐ผ๐๐๐ฒ ๐๐ฟ๐ฎ๐ถ๐ป๐ถ๐ป๐ด ๐ฝ๐ฟ๐ผ๐ด๐ฟ๐ฎ๐บ ๐ณ๐ผ๐ฟ ๐๐๐ ๐ ๐ฒ๐ฑ๐ถ๐ฐ๐ฎ๐น ๐ฆ๐ฑ๐ป ๐๐ต๐ฑ, held from ๐ฎ๐ฑ โ ๐ฎ๐ต ๐๐๐ด๐๐๐ ๐ฎ๐ฌ๐ฎ๐ฑ.
This program was designed to strengthen knowledge, skills, and compliance in sterile medical device manufacturing, focusing on:
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Sterilization methods with emphasis on Ethylene Oxide (ETO) sterilization.
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Validation and routine control monitoring in compliance with ISO 11135.
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Sterile barrier systems and packaging validation based on ISO 11607 Parts 1 & 2.
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Microbiological and chemical testing: bioburden, sterility, EO residuals, endotoxin, and biocompatibility (ISO 11737, ISO 10993 series).
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Alignment with international standards and regulatory requirements to ensure product safety and patient protection.
The training combined lectures, interactive workshops, and practical assessments, ensuring participants gained both theoretical understanding and hands-on competence. Certificates of completion were awarded to all successful participants.
ARG is proud to support CCB Medicalโs commitment to quality, compliance, and continuous improvement in sterile medical device manufacturing.
๐๐ ๐๐ฅ๐, ๐ผ๐๐ฟ ๐บ๐ถ๐๐๐ถ๐ผ๐ป ๐ถ๐ ๐๐ผ ๐ฑ๐ฒ๐น๐ถ๐๐ฒ๐ฟ ๐๐๐๐๐ฟ๐ฎ๐ป๐ฐ๐ฒ, ๐ฅ๐ฒ๐ฐ๐ผ๐ด๐ป๐ถ๐๐ถ๐ผ๐ป & ๐๐ฟ๐ผ๐๐๐ต ๐๐ผ ๐ผ๐๐ฟ ๐ฐ๐น๐ถ๐ฒ๐ป๐๐ ๐๐ต๐ฟ๐ผ๐๐ด๐ต ๐๐ผ๐ฟ๐น๐ฑ-๐ฐ๐น๐ฎ๐๐ ๐๐ฟ๐ฎ๐ถ๐ป๐ถ๐ป๐ด ๐ฎ๐ป๐ฑ ๐ฐ๐ฒ๐ฟ๐๐ถ๐ณ๐ถ๐ฐ๐ฎ๐๐ถ๐ผ๐ป ๐๐ฒ๐ฟ๐๐ถ๐ฐ๐ฒ๐.
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