Recognizing the rise of complex biologics and combination products, as well as tightened cGMP requirements, aseptic processing and sterile manufacturing are second to none for quality products and patients’ safety. Through a series of technical and commercial case studies, the 3-day summit will:
– Understand GMP requirements to ensure compliance at all times
– Assess the latest technologies to enhance sterility assurance and manufacturing efficiency
– Benchmark against best practice of risk assessment for your aseptic processing
This must attend forum will give you access to practical case studies providing actionable insights which you can implement immediately to avoid pitfalls.