DIA Middle East CMC Conference 2016

Topics

• Counterfeits / Falsified Medicines: State of Regulation & Standards, examples of successful implementation of traceability
• Pharmaceutical product life cycle – key aspects of the ICH Q12 guideline, best practice, and risks to avoid
• How to handle CMC requirements to accelerate approval pathway
• Learnings from the regional implementation of Serialization
• Ensure inspection readiness of your processes, premises, and products

Who should Attend

Attendees involved or interested in:

• Chemistry Manufacturing & Control specialists
• Pharmaceutical technical & quality personnel
• Life cycle management specialists
• Project and product managers
• Regulatory submission and maintenance staff
• Supply chain management staff
• Clinical Research R&D specialists