Technical Courses
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Specialist programmes focusing on excellence in tableting, process control, statistics and other discliplines. To make suggestions about courses you would like to see, please use the contact form.
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Integrated Tablet Formulation Development |
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Tablet Process Development and Validation and the application of QbD |
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Development and manufacture of effervescent tablets |
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Stability Testing in Pharmaceutical Development and Manufacturing |
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Introduction to Photostability |
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Analytical Method development and Validation |
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GMP Auditor Training |
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How to Audit API Manufacturers |
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Writing effective SOPs in a GMP environment |
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OOS investigations in a GMP environment |
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Pharmaceutical Documentation - a practical approach |
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Supply Chain Management - Pharma/Biotech |
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Pharmaceutical Documentation - a practical approach |
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CAPA and OOS Investigations |
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An Integrated Approach to Pharmacokinetics in Drug Development |
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Validation of Computerised Systems |
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Hands-On Tabletting |
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The Challenges and Formulation Strategies for Poorly Soluble Drug Substances |
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Active Pharmaceutical Ingredients - Development, Supply and Commercial Manufacture |
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Introduction to Lean 6 Sigma |
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Effective Investigation and CAPA |
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Handling API Manufacturing Deviations |
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How to Certify API Compliance |
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How to Manage Regulatory Inspections |
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ICH Q7 / Part II EU GMP Guide - Essential GMP Guide for APIs |
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Update on EU GMP GMP Guidelines and Inspection Procedures |
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CAPA in the pharma industry |
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Annex 13 |
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Annex 16 |
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Technology Transfer |
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Supplier Management |
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For any enquiries, contact us on +44 20 7613 7232 Email
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