With many years of successfully designing, developing and implementing electronic systems in a regulated environment for a wide array of clients, SeerPharma now offers these services for your software implementations.
The STEMM Central Bootcamp is a program jointly administered by the Cancer Therapeutics CRC and Biomedical Research Victoria.
One of our senior GMP consultants was invited to represent SeerPharma at Singapore Polytechnic to address final year students pursuing a Diploma in Biotechnology.
SeerPharma Singapore in collaboration with SPRING Singapore rolled out a series of GxP Consultancy and Training modules for the manufacturers of traditional medicines.
A number of our clients have turned to SeerPharma over the last few months looking for short term contract resources to assist with Quality Assurance roles. Our current cohort of contractors are helping clients with overall Quality Systems Management, Product Life Cycle Management, Documentation, and Validation work.
The European Directives on medical devices have been replaced by a Medical Device Regulation (MDR), which came in to effect April 2017.
A major focus of the post-graduate courses in Good Manufacturing Practice (GMP) SeerPharma deliver at the University of Technology Sydney (UTS) is skill-building for the real-world.
This post was first published in July 2017 and has been updated to reflect changes.
The Therapeutic Goods Administration (TGA) is part of the Australian Federal Government’s Department of Health and is responsible for regulating the supply, import, export, manufacturing and advertising of therapeutic goods, including medicines
Good Manufacturing...
SeerPharma is assisting a number of start-up biotech companies with implementing a basic Quality Assurance Plan (QAP) – a building block of a fully-fledged Quality Management System. The QAP can be put in place to grow as companies mature.
Kicking off 2017 saw SeerPharma deliver our most popular course “Introduction to GMP” across the Asia-Pacific region.
