SeerPharma are a team of consultants that provide advice, training, software and contract labour resources to pharmaceutical, medical device and life science companies in the Asia-Pacific region on matters of Quality Assurance and GMP compliance. We have been serving our clients in the Asia-Pacific region for over 25 years from our offices in Melbourne, Sydney and Singapore and are also able to provide assistance in Europe through our affiliate in the UK.
Our team of consultants have extensive experience working with clients supplying, or looking to enter the supply chain of a therapeutic product. We work with organisations looking to ensure that their facilities, equipment, quality systems and processes are compliant with FDA, PIC/S, TGA, WHO, ISO, ICH and other regulations and standards that apply to their product(s). Our consultants actively train and provide advice to companies on matters of compliance from Research and Development through to Manufacturing, Logistics, Warehousing and Post Market Surveillance. We regularly inspect organisations on behalf of the Australian Government (APVMA) as well as Pharmaceutical and Medical Device organisations relying on suppliers in the Asia-Pacific region. Our software team routinely implement electronic Quality Management Systems to help improve process efficiencies within organisations. Companies also turn to SeerPharma to provide short term Quality Assurance contractors to help with projects that do not warrant hiring a full or part time employee.
Through our engagement we have made companies in the Asia-Pacific region compliant; upskilled existing capabilities and improved operational efficiencies. SeerPharma are proud to be known in the market as “Asia-Pacific’s Leader in Quality Assurance and GMP solutions” for the Pharmaceutical and Medical Device Industry.
Contact us to explore how you can leverage our skills and services to support your business needs.