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GMP and Compliance
Development of Stability-Indicating HPLC Methods
GMP Auditor Training for Quality Systems
Parenteral Products
Pharmaceutical Aerosols, Dry Powder Inhalation Systems and Nasal Delivery Devices
Pharmaceutical Dissolution Testing - a 2 day course
Pharmaceutical Granulation and Compression
Pharmaceutical Product Development
Pharmaceutical Manufacturing Support
In-house Training Courses
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Chiral Analysis by Chromatography
Developing Pharmaceutical Tablets for Low Cost Manufacturing
Development and Manufacture of Effervescent Tablets
Development of Stability-Indicating HPLC Methods
Gas chromatography: theory and practice for residual solvents testing
GMP Auditor Training for Quality Systems
GMP in Primary (API) Manufacturing
Hands-on Tablet Development including the principles of pre-formulation, formulation and process dev
How to Audit API Manufacturers
HPLC Analytical Method Development and Validation
In-house Training Courses
Integrated Tablet Formulation Development
Introduction to LC-MS for Pharma Industry
Introduction to Photostability
Introduction to Sterile Product Manufacture for New Starters and Junior Staff
Introduction to Sterile Product Manufacture for those with a cGMP basic understanding
Introduction to the Formulation & Stabilisation of Protein and Peptide Drugs
Latest Advances in the Stabilisation and Formulation of Protein and Peptide Drugs
Molecules to Market
OOS Investigations in a GMP Environment
Oral Solid Dosage Manufacturing Technology
Parenteral Products
Pharmaceutical Aerosols, Dry Powder Inhalation Systems and Nasal Delivery Devices
Pharmaceutical Dissolution Testing - a 2 day course
Pharmaceutical Dissolution Testing - a Hands-on course
Pharmaceutical Granulation and Compression
Pharmaceutical Packaging - an introductory course
Pharmacokinetics in Drug Development - an integrated approach
Pharmacokinetics in special populations
Planning for Commercial Launch
Powder Technology for Pharmaceutical Development and Manufacturing
Preformulation Studies for Tablet Development
QbD and Lifecycle Management for Analytical Methods
Residual solvents: regulatory requirements, method development and validation
Stability Analysis for the Pharmaceutical Industry
Stability Testing in Biological Product Development and Manufacturing
Stability Testing in Pharmaceutical Development and Manufacture
Supply Chain Management in Pharma/Biotech
Supply Chain Risk Management and Compliance for QPs and RPs
Tablet Formulation Development
Tablet Formulation Development - Formulation development in practice
Tablet Process Development, Validation and the Application of QbD
Team building and decision-making
Technology Transfer
Training Course Programme 2018
Understanding Isomers, Stereochemistry and Chirality
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