<p><img class="alignnone size-full wp-image-3170" src="https://cm.base-asia.com/wp-content/uploads/2021/03/45001.png" alt="" width="168" height="238" /> <img class="alignnone size-full wp-image-3169" src="https://cm.base-asia.com/wp-content/uploads/2021/03/13485.png" alt="" width="169" height="237" /></p><p>We are a contract manufacturer certified under the ISO 13485:2016 and ISO 45001:2018 certifications.</p><div class="textblock-shortcode clear"><p>These certifications indicate that our quality management system maintains stringent international standards for medical devices, including in vitro diagnostic assays.</p><p>To be certified ISO 13485 and ISO 45001, our materials, processes, products and services underwent rigorous and independent testing for safety, product performance or reliability.</p><p>View our list of ISO certifications here:</p><ul><li><a href="https://axilscientific.com/downloads/news/Cert-%20Axil%20Scientific%20Pte.%20Ltd.%20ISO%2013485%202016_SAC.pdf">ISO 13485:2016</a></li><li><a href="https://axilscientific.com/downloads/news/Cert-%20Axil%20Scientific%20Pte.%20Ltd.%20ISO%2045001%202018_UKAS.pdf">ISO 45001:2018</a></li></ul></div><div class="fw-divider-space"> </div><div class="textblock-shortcode clear"><p>We follow strict SOPs for production and QC. Our ISO standard quality management ensures traceability and documentation in every process of the project.</p><ul><li>Traceability and Documentation</li><li>Risk assessment and Evaluation</li><li>Verification and Validation of Products and Processes</li></ul></div>

<div class="fw-main-row"><div class="fw-container"><div class="fw-row"><div class="fw-col-xs-12 "><div class="seo-media-images"><img src="//cm.base-asia.com/wp-content/uploads/2021/03/Clean-Room.jpg" alt="//cm.base-asia.com/wp-content/uploads/2021/03/Clean-Room.jpg" width="600"></div></div></div><div class="fw-row"><div class="fw-col-xs-12 "><div class="fw-divider-space" style="margin-top: 50px"></div></div></div></div></div><div class="fw-main-row"><div class="fw-container"><div class="fw-row"><div class="fw-col-xs-12 "><div class="textblock-shortcode clear"><p>1st BASE facility offers ISO clean room capabilities for customers who need their product parts processed in an extremely clean, controlled environment.</p><p><strong>Clean Room</strong></p><p>Operational capacity of more than 550 square meter and 4 separate ISO Class7 cleanrooms of over 270bsqyuare meters. Our ISO Class 7 Cleanroom enables ideal environments for biotechnology, pharmaceutical, food processing and other applications requiring high level of cleanliness. Clean rooms control air quality and the level of debris and particulates that are present in the chamber by filtering the air through a HEPA filter, which pressurizes the room and removes 99.9% of all particles — an extremely important factor in applications for which cleanliness is integral.</p><p><strong>Controlled Environments</strong></p><p>At the same time, 1st BASE offer various other controlled manufacturing environments (HEPA & non-HEPA filtered conditions) including laminar flow devices, chemical fume hoods, biological safety cabinets, PCR cabinets. Some cleanroom work requires the protection of people from hazardous substances, such as liquid or solid chemicals or biological agents. 1st BASE’s various controlled environment module enables:</p><ul><li>Personal Protection from harmful agents within the cabinet</li><li>Product Protection to avoid contamination of the samples.</li><li>Environmental Protection from contaminants contained within the cabinet.</li></ul><p><strong><br />Maintenance & Certifications<br /></strong></p><ul><li>Certified by national and international standards.</li><li>Monitoring of cleanroom standards</li></ul></div></div></div></div></div><div class="fw-main-row"><div class="fw-container"><div class="fw-row"><div class="fw-col-xs-12 "><div class="fw-divider-space" style="margin-top: 50px"></div></div></div></div></div><p><!-- a98a3c6a5b04be517e8c147587c5fb10 --></p>