ADVANCING QUALITY AND GMP BEST PRACTICES IN THE ASIA-PACIFIC REGIONConsulting | Training | MasterControl | ContractingSeerPharma is a team of consultants that provide best-practice advice, training, software solutions from MasterControl, and contract labour resources to pharmaceutical, medical device and life science companies in the Asia-Pacific region on matters of Quality and GMP compliance. We have been serving our clients in the Asia-Pacific region for over 30 years from Melbourne, Sydney and Singapore and are also able to provide assistance in Europe through our affiliate in the UK.Our team of consultants has 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 IT Solutions 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 work we aim to "Advance Quality and GMP Best Practices in the APAC region" for the Pharmaceutical and Medical Device Industries.Contact us to explore how you can leverage our skills and services to support your business needs.

Facility Design & Licensing Pharmaceuticals (all dosage forms | sterile | non-sterile) Quality Medical Devices (all classes) GMP Risk Management Audits | Inspections Validation Planning and Execution Quality Management Systems Productivity Facility Design & Licensing Operational Compliance QA GMP Audits Inspections Gap Assessments Quality Assurance GMP Training PIC/S GMP US FDA GMP Electronic Quality Management Systems Computer System Validation ICH Online GMP Training IT Project Mentoring for Regulated Industries Facility Design & Licensing