Technical Courses

 

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.

 

 

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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