The DIA Middle East CMC Conference 2016 covers topics such as:
- 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
The DIA Middle East CMC Conference 2016 brings together 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
