Students enrolled in our Postgraduate Good Manufacturing Practice (GMP) Program at UTS engage in a range of subjects, each spanning 10 weeks and guided by our Consulting team. Throughout their studies, they delve into various topics, such as International GMPs and QA, Validation Principles, GxP, Quality Auditing, and Computer Systems Validation.
The launch of new temperature sensitive biologics, increasing regulations, growing cost- pressures are putting more complex demands on the biopharma industry’s high-stakes logistics environment.
As a manufacturer or sponsor of a pharmaceutical and/or medical device, you need to ensure control over component and product quality, as well compliance with legal and customer requirements. Establishing and maintaining a supplier quality assurance program can be a challenge, with regulatory requirements and supply chain complexity continuing to...
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