SeerPharma Singapore in collaboration with SPRING Singapore rolled out a series of GxP Consultancy and Training modules for the manufacturers of traditional medicines.
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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The European Directives on medical devices have been replaced by a Medical Device Regulation (MDR), which came in to effect April 2017.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.
Asia’s biopharmaceutical industry has evolved from a manufacturing destination to a goto market for clinical development and a hotbed of innovation. Asia contains some of the world’s leading pharma and biopharma markets on the planet.
SeerPharma has commenced work assisting a firm looking to manufacture and supply multivitamin tablets to China and Australia. Our team has been engaged to help obtain a TGA GMP license by ensuring that the manufacturer has a suitable Quality Management System and will alsohelp ensure that the facility and equipment the firm plans on using is...
Pharmacists are expected to be aware of and comply with relevant practice standards and guidelines on compounding. Despite certain exceptions, compounded medicines must meet the quality standards set out in the Therapeutic Goods Act 1989 (Cth).
