The University of Technology Sydney (UTS) has scheduled postponed the first "Introduction to Bioprocessing" training session in the new 430m2 Biologics Innovation Facility (BIF) with its cGMP designed clean rooms and containment laboratories.
SeerPharma’s training division grows from strength to strength with several companies requesting tailored on-site QA/GMP training for staff. Recently a major multinational pharmaceutical manufacturer approached SeerPharma to address the following key areas of interest for staff at their firm:
Marissa Ryan, Joan Semmler, Dr Christine Carrington, Princess Alexandra Hospital, Brisbane, Australia.1
The Sterile Production Centre (SPC) at the Princess Alexandra Hospital (PAH) has one of the few hospital-based production facilities in Queensland. The Society of Hospital Pharmacists of Australia (SHPA) Guidelines for Medicines Prepared in...
SeerPharma routinely deliver publicly scheduled GMP training in Australia, New Zealand and Singapore, with our flagship course GMP - What You Need To Know (SP6510) being one of the most sought-after programs in our schedule.
A manufacturer of pharmaceuticals in the Asia-Pacific region engaged SeerPharma to deliver an onsite training workshop on Data Integrity to staff involved in Production, Quality and Warehousing.
SeerPharma have partnered with Temasek Polytechnic’s Centre of Innovation for Complementary Health Products (COI-CHP), to assist companies involved with Pharmaceuticals, Biologicals, Complementary Medicines, Traditional Chinese Medicine and Cosmetics, help ensure their Facilities and Operations are GMP compliant; their products are manufactured...
Kalbe Farma is a leading healthcare provider in Indonesia, with extensive operations throughout the South East Asian region. Its’ subsidiary PT Kalbio Global Medika (KGM) has recently opened a new 11,000 square meter factory in Indonesia, which received a Honourable Mention for the 2017 Facility of the Year Awards from ISPE.
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).
Major pharmaceutical companies in the Asian region requested assistance with GMP supplier audits .
SeerPharma Singapore was the selected vendor and training partner to conduct introductory Good Manufacturing Practices (GMP) training for the BioProcessing Technology Institute (BTI) of Singapore.
