At Cook Medical, we are passionate about making unique, quality medical devices and connecting with people to improve lives. Founded on inventing, manufacturing and delivering medical devices, we provide healthcare professionals with the tools they need to help their patients return to living.
In Australia, Cook employs more than 800 people and is one of Queensland’s largest medical device manufacturers and exporters. We export 94% of our locally manufactured products to medical providers around the world with devices across two product families: endovascular grafts for the treatment of vascular disease and in-vitro fertilisation to assist those trying to conceive a child. Both product lines were invented and developed in Australia. The former developed in partnership with Perth-based vascular clinicians, and the latter with pioneering IVF units in Melbourne and Sydney.
As part of a global network of companies, Cook offers a range of state-of-the-art treatment options for physicians and patients in Australian hospitals. This broad product offering supports both diagnostic and minimally invasive therapeutic procedures, serving nearly 60 clinical specialties, reaching almost every area of the hospital.

West Pharmaceutical Services, Inc. is a leading provider of innovative, high-quality injectable solutions and services. As a trusted partner to established and emerging drug developers, West helps ensure the safe, effective containment and delivery of life-saving and life-enhancing medicines for patients. With over 10,000 team members across 50 sites including 26 manufacturing facilities worldwide, West helps support our customers by delivering over 41 billion components and devices each year. Headquartered in Exton, Pennsylvania, West in 2025 generated $3.1 billion in net sales. West is traded on the New York Stock Exchange (NYSE: WST) and is included in the Standard & Poor's 500 index. For more information, visit www.westpharma.com.

Website links
Corporate site: https://www.westpharma.com/
Blog: https://www.westpharma.com/blog

Social Media links
LinkedIn: https://www.linkedin.com/company/west-pharmaceutical-services/posts/?feedView=all
YouTube: youtube.com/user/WestFYI

SeerPharma is a private consulting organisation supporting medical device and pharmaceutical companies across the Asia-Pacific (APAC) region with expertise in Quality Systems, regulatory compliance, and Good Manufacturing Practice (GMP). With more than 35 years of experience, the company works with organisations involved in the development, manufacture, and lifecycle management of regulated healthcare products, with a strong focus on helping medical device companies maintain compliance and operational excellence.

Operating with team members in Melbourne, Sydney, Singapore, and India, plus supported by an affiliate in the United Kingdom, SeerPharma assists organisations in establishing and maintaining effective quality and regulatory frameworks. The team helps ensure that facilities, equipment, processes, and computerised systems meet the expectations of global regulatory authorities and standards bodies, including the FDA, TGA, EMA, WHO, PIC/S, ISO, and ICH. For medical device organisations, this includes supporting alignment with ISO 13485 and other regulatory requirements governing device design, manufacturing, and post-market oversight.

SeerPharma regularly supports medical device companies in preparing for and responding to regulatory inspections and audits from authorities such as the Therapeutic Goods Administration (TGA), the U.S. Food and Drug Administration (FDA), and European regulators. The team also performs independent supplier and GMP audits across the Asia-Pacific region on behalf of industry clients and in preparation for Notified Bodies. These activities help organisations strengthen supply chain oversight and ensure ongoing compliance in a highly regulated environment.

Training and capability development are key components of SeerPharma’s services. The firm provides practical training in quality and GMP compliance across the product lifecycle, from research and development through manufacturing, distribution, and post-market surveillance. This commitment to professional development has led SeerPharma to develop and deliver an internationally recognised Postgraduate GMP Program at the University of Technology Sydney (UTS), supporting professionals working in pharmaceutical and medical device sectors throughout the APAC region.

SeerPharma also helps organisations modernise their quality systems through digital transformation initiatives. Its Software Solutions team implements electronic Quality Management Systems (eQMS) and paperless manufacturing solutions using the MasterControl platform. These solutions help medical device manufacturers streamline processes, improve documentation control, and strengthen their ability to demonstrate regulatory compliance.

In addition to consulting and technology services, SeerPharma provides experienced Quality Assurance and compliance professionals on a contract basis. These specialists support projects such as quality system implementation, remediation activities, inspection readiness, and process improvement initiatives where short-term expertise is required.

Through its consulting, training, technology, and resourcing services, SeerPharma aims to
“Advance Quality and GMP best practices in the APAC region”, supporting medical device organisations in delivering safe, effective, and compliant products to global markets.

www.seerpharma.com