INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2022.
When manufacturing pharmaceuticals, the risk of contaminants impacting pharmaceutical safety, efficacy and purity is real.
For over 7 years, SeerPharma has partnered with the University of Technology Sydney’s Graduate School of Health, to offer internationally recognised Postgraduate Qualifications in Good Manufacturing Practice (GMP). Our partnership with UTS grows from strength to strength.In 2020, we established the SeerPharma Scholarship to support working...
Orioled Hub is a group of companies established in Singapore, Hongkong, Latvia and Vietnam - merging pharmaceutical and financial companies with more than 20 years of experience in the pharmaceutical market. Orioled Hub is the representative, distributor, and preferred partner of many worldwide companies from the US, Europe and Japan to the South...
The 2022 PDA Pharmaceutical Manufacturing & Quality Conference is an in-person event that will be held on 6-7 September 2022 in Singapore.
The Parenteral Drug Association (PDA) is the leading global provider of science, technology and regulatory information and education for the pharmaceutical and biopharmaceutical community. Founded in 1946 as a non-profit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance...
Personnel behaviour plays a significant role in the manufacture of sterile products. Aseptic processing occurs under a Laminar Air Flow, which is classified as a Grade A or ISO 4.8 environment. Disturbance of air in the Laminar Air Flow can affect the quality of the final product.
SeerPharma has been at the forefront of delivering GMP Training to the Pharmaceutical and Medical Device industries since the 1990s. With a constant view to the future, SeerPharma pioneered its own eLearning solution for industry and developed a Learning Management System (LMS) that hosted GMP eLearning courses and assessments. The solution was...
I was born and raised in Ghana. I have a Bachelor of Science in Chemistry, and I'm married with a six-year-old kid.Since 2010, I've worked for Ghana's Food and Drugs Authority (FDA), which is the National Medicines Regulatory Agency (NMRA). My principal job responsibility as a senior regulatory officer at the FDA's Drugs Inspectorate Department is...
In 2014, the FDA issued a guidance document for the Management of Cybersecurity in Medical Devices – Content of Premarket Submissions. Since then, technologies and the interconnectivity of medical devices have evolved rapidly. In response, the FDA released a new draft guidance in April 2022, for comment purposes only - Cybersecurity in Medical...
