{"id":3558,"date":"2020-09-18T14:37:00","date_gmt":"2020-09-18T14:37:00","guid":{"rendered":"https:\/\/sites.generatepress.com\/wired\/?page_id=3558"},"modified":"2026-01-15T12:05:46","modified_gmt":"2026-01-15T02:05:46","slug":"services","status":"publish","type":"page","link":"https:\/\/silpharma.com\/index.php\/services\/","title":{"rendered":"Services"},"content":{"rendered":"\n<div class=\"gb-element-24cbd4e3\">\n<div class=\"gb-element-ed301a02\">\n<h2 class=\"gb-text gb-text-80950bbd\">At SIL Pharma<\/h2>\n\n\n\n<p>We help pharmaceutical, biotech, and clinical research organisations build and maintain robust, compliant, and audit-ready quality systems. With expertise in GMP, GCP, and ISO requirements, we provide end-to-end support in QA compliance, risk and gap assessments, supplier audits, and technical writing \u2014 ensuring your operations are aligned, efficient, and audit-ready.<\/p>\n<\/div>\n\n\n\n<div class=\"gb-element-fed8a4ca\">\n<ul class=\"wp-block-list\">\n<li><a href=\"https:\/\/silpharma.com\/index.php\/services\/#id-1\" data-type=\"page\" data-id=\"3558\">Suppliers Quality Audits<\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/silpharma.com\/index.php\/services\/#id-2\">QA Compliance<\/a><\/li>\n\n\n\n<li>Support for Clinical Trials <\/li>\n\n\n\n<li><a href=\"https:\/\/silpharma.com\/index.php\/services\/#id-4\" data-type=\"link\" data-id=\"https:\/\/silpharma.com\/index.php\/services\/#id-4\">Technical writing<\/a><\/li>\n\n\n\n<li>Validation &amp; Technology Transfer Services<\/li>\n<\/ul>\n<\/div>\n<\/div>\n\n\n\n<div class=\"gb-element-6ed9bd82\">\n<div class=\"gb-element-5914a6b4\">\n<h2 class=\"wp-block-heading\" id=\"id-1\">Suppliers Quality Audits<\/h2>\n\n\n\n<p>We provide professional Quality Management System (QMS) auditing services to ensure compliance, efficiency, and continual improvement. With over 25 years of experience in the pharmaceutical and clinical research sectors, we conduct audits aligned with GMP regulatory requirements, GCP guidelines and ISO standards and to identify gaps, assess risks, and strengthen quality systems.<\/p>\n\n\n\n<p>Our auditors hold Certified Quality Auditor (CQA) certification and apply a standardised approach to ensure efficient, effective, and value-driven assessments. Our audits go beyond compliance as we focus on improving processes, supporting regulatory readiness, and fostering a culture of quality that drives better processes and products.&nbsp;<\/p>\n<\/div>\n\n\n\n<div class=\"gb-element-374bf8db\">\n<h2 class=\"wp-block-heading\" id=\"id-2\">QA Compliance<\/h2>\n\n\n\n<p>We provide expert Quality Assurance (QA) compliance services to help organisations maintain robust, audit-ready quality management systems that meet regulatory requirements and industry standards. We ensure alignment with GMP, GCP and ISO requirements through practical and risk-based approaches.<\/p>\n\n\n\n<p>Our approach is to work collaboratively with our clients to strengthen their quality systems, streamline processes, investigate and close non-conformances\/CAPAs, prepare risk assessment and foster a culture of continuous improvement and regulatory excellence.<\/p>\n<\/div>\n<\/div>\n\n\n\n<div class=\"gb-element-708d9646\">\n<div class=\"gb-element-728f6558\">\n<h2 class=\"wp-block-heading\" id=\"id-3\">Support for Clinical Trials <\/h2>\n\n\n\n<p>We provide expert support in the development of high-quality documentation for Human Research Ethics Committee (HREC) submissions and clinical trial management. We assist sponsors, researchers, and clinical teams by preparing clear, compliant, and well-structured submission packages, including study protocols, Participant Information and Consent Forms (PICF), Investigator Brochures (IB), and associated regulatory and quality documents. <\/p>\n\n\n\n<p>In addition, we support clinical trial planning, site start-up, vendor oversight, study coordination, and compliance activities to ensure projects run efficiently and meet regulatory expectations.<\/p>\n<\/div>\n\n\n\n<div class=\"gb-element-5d37bfa6\">\n<h2 class=\"wp-block-heading\" id=\"id-4\">Technical Writing<\/h2>\n\n\n\n<p>We provide professional technical writing services tailored to the quality management systems in the pharmaceutical, clinical research, and medical device sectors.<\/p>\n\n\n\n<p>Our focus is on clarity, accuracy, and practicality \u2014 ensuring every document communicates complex information effectively while meeting regulatory and organisational requirements.<\/p>\n<\/div>\n<\/div>\n\n\n\n<div class=\"gb-element-15195352\">\n<div class=\"gb-element-dbf6a494\">\n<h2 class=\"wp-block-heading\" id=\"id-1\">Validation &amp; Technology Transfer Services<\/h2>\n\n\n\n<p>We provide comprehensive technology transfer and scale-up activities including validation services designed to support pharmaceutical manufacturing operations with practical, well-organised approaches that align with real-world production needs. Our expertise spans process validation, equipment qualification, and cleaning validation.<\/p>\n\n\n\n<p>Our services include process validation execution, cleaning and packaging validation, equipment qualification (IQ\/OQ\/PQ) and development of validation documentation and reports. We also provide expert support during audits and regulatory inspections.<\/p>\n\n\n\n<p>Our focus is on delivering reliable, fit-for-purpose solutions that meet regulatory requirements while making validation activities more manageable and integrated into daily operations.<\/p>\n<\/div>\n\n\n<\/div>\n\n\n\n<div class=\"gb-element-da32a0c7\">\n<h3 class=\"gb-text gb-text-e4b672f3\">Ready to streamline your quality and regulatory journey?<\/h3>\n\n\n\n<a class=\"gb-text-3769e1a2\" href=\"https:\/\/silpharma.com\/index.php\/contact\/\"><span class=\"gb-text\">Contact us<\/span><span class=\"gb-shape\"><svg aria-hidden=\"true\" height=\"1em\" width=\"1em\" viewBox=\"0 0 256 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path fill=\"currentColor\" d=\"M224.3 273l-136 136c-9.4 9.4-24.6 9.4-33.9 0l-22.6-22.6c-9.4-9.4-9.4-24.6 0-33.9l96.4-96.4-96.4-96.4c-9.4-9.4-9.4-24.6 0-33.9L54.3 103c9.4-9.4 24.6-9.4 33.9 0l136 136c9.5 9.4 9.5 24.6.1 34z\"><\/path><\/svg><\/span><\/a>\n<\/div>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>At SIL Pharma We help pharmaceutical, biotech, and clinical research organisations build and maintain robust, compliant, and audit-ready quality systems. With expertise in GMP, GCP, and ISO requirements, we provide end-to-end support in QA compliance, risk and gap assessments, supplier audits, and technical writing \u2014 ensuring your operations are aligned, efficient, and audit-ready. Suppliers Quality &#8230; <a title=\"Services\" class=\"read-more\" href=\"https:\/\/silpharma.com\/index.php\/services\/\" aria-label=\"Read more about Services\">Read more<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-3558","page","type-page","status-publish"],"_links":{"self":[{"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/pages\/3558","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/comments?post=3558"}],"version-history":[{"count":22,"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/pages\/3558\/revisions"}],"predecessor-version":[{"id":4443,"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/pages\/3558\/revisions\/4443"}],"wp:attachment":[{"href":"https:\/\/silpharma.com\/index.php\/wp-json\/wp\/v2\/media?parent=3558"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}