SeerPharma are a team of over 30 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. The company has been serving clients in the Asia-Pacific region for over 25 years from their offices in Melbourne, Sydney and Singapore and are also able to provide assistance in Europe through their affiliate in the UK. The team have extensive experience working with clients supplying, or looking to enter the supply chain of a therapeutic product.
The company works 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). Through engagement they have made companies in the Asia-Pacific region compliant; upskilled existing capabilities and improved operational efficiencies.