Efficiency, compliance, and precision form the foundation of Good Manufacturing Practice (GMP) in medicines manufacturing. From specialised GMP equipment that ensures product quality and consistency to precision production scales, each component plays a crucial role in maintaining high industry standards.
Effective materials handling solutions streamline workflows, reduce waste, and improve workplace safety by minimising contamination risks and enhancing operational efficiency. Meanwhile, advanced manufacturing processes integrate automation, real-time quality control, and cutting-edge innovations to maximise productivity and scalability.
Whether producing chemical pharmaceuticals, biologics, cell and gene therapies, or vaccines, the right combination of equipment, materials handling strategies, and process controls is essential for meeting stringent regulatory standards and ensuring the reliable delivery of safe, high-quality medicines to patients worldwide.
Learning outcomes
Classroom understanding of:
• USP equipment at different scales
• DSP equipment at different scales
• Analytic equipment for medicines production
• Storage and shipping technology
• Validating equipment
• Raw materials and supply chain
• Receipting and bill of goods
Practical experience in:
VR/MR experience, immersive visualisation of typical process, Bioreactor setup, Core processes for production, Standard operating procedures and operating guidelines.
Who should attend:
Anyone with an interest in working in GMP medicines manufacturing, Quality in GMP, graduates or research scientists looking to establish their career in GMP/ ATMP industry.
Duration:
2 days in person
Registration:
Email: [email protected]
