• Product synthesis
• Formulation development: solutions, suspensions, powders, tablets & capsules including slow release formulations
• Process Validation: pilot scale batches
• Stability studies: protocols compiled according to ICH Guidelines
• Bio equivalence studies: monitor & write Expert Reports
• Registration dossiers: according to CTD format
• Process Validation: commercial scale batches
• Packaging of product
• Consultancy service
• Analytical development and validation
General Manager – Chanelle Pharma Labs Jordan
Chanelle Pharma Group
Dublin Road, Loughrea,
Co Galway, Ireland.
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