Resources | Cell Therapy Manufacturing and Process Development

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cGMP Guidelines

Find out more about the current Good Manufacturing Practices, and regulations set forth by the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Health Sciences Authority (HSA), International Council for Harmonisation (ICH), Standards Coordinating Body (SCB), Alliance for Regenerative Medicines (ARM), Therapeutics Goods Administration (TGA), Pharmaceuticals and Medical Device Agency (PMDA) and Pharmaceutical […]

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Clinical Trial and Beta Testing

Clinical trials are essential stages for the testing of cancer therapies to ensure the safety and efficacy of the new findings, it involves the investigation of the effectiveness of new treatment. Beta testing is carried out before launch, it serve as a trial period for individual users (“beta testers”) to have a real-world exposure.

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CTGT TRANSLATIONAL RESEARCH

CTGT Translational Research focuses on efforts to build on basic scientific research carried out by clients or in-house R&D team to create new CTGT products by offering services such as: (i) process gap analysis; (ii) process development; (iii) process improvement; (iv) process validation; (v) process verification; (vi) SOP establishment; (vi) process implementation in cGMP; […]

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Learning Portal

Learning Portal, an online catalogue of our training and education initiatives, provides you an easy way to explore different programmes that would best fit your learning needs and preferences.

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