A decade ago, Duke-NUS Medical School established the Centre of Regulatory Excellence (CoRE) to enhance health products regulatory systems and competency across ASEAN and the broader Asia-Pacific region. CoRE is pivotal in supporting policy innovation and facilitating progress towards effective and efficient health products regulation. As a...
SeerPharma consults on 100 to 150 projects every year. Many of these engagements with pharmaceutical and medical device companies involve providing ongoing support for business needs related to Quality Assurance (QA) and Good Manufacturing Practice (GMP) compliance. Our clients continue to rely on our expertise for regular remote and on-site...
INFOGRAPHIC: A snapshot of how SeerPharma supported its clients with Quality and GMP Best-Practices in 2023 through QA & GMP Consulting, Auditing, Training and MasterControl "Qx" electronic Quality Management Systems (eQMS) & "Mx" Manufacturing Execution Systems (MES) with electronic Batch Records (eBR).
A leading pharmaceutical manufacturer in Vietnam requested SeerPharma to conduct an on-site review of a manufacturing line, in preparation for an impending European Union (EU) Good Manufacturing Practice (GMP) inspection.
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2022.
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.
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2021.
Human Error is the propensity for certain common mistakes by people; the making of an error as a natural result of being human. Human errors cannot be stopped by wishing they would not happen. The extent of knowledge, training and level of skill has little to do with the mistakes we make. However, most human Error is PREVENTABLE. Our systems and...
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2020.
The Pharmaceutical and Medical Device industries rely on a fragmented and complex supply chain to get product in to market. Your organisation or your suppliers could be conducting a single step or multiple steps of manufacture, and as such must adhere to the principles of GMP that apply to your operation and the market in which your product is...
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