- GMP and Compliance
- In-house Training Courses
- Pharmaceutical Dissolution Testing - a 2 day course
- Introduction to Sterile Product Manufacture for those with a cGMP basic understanding
- Tablet Formulation Development
- Understanding Isomers, Stereochemistry and Chirality
- Pharmacokinetics in special populations
- Residual solvents: regulatory requirements, method development and validation
- Chiral Analysis by Chromatography
- Introduction to LC-MS for Pharma Industry
- Gas chromatography: theory and practice for residual solvents testing
- Preformulation Studies for Tablet Development
- Introduction to Sterile Product Manufacture for New Starters and Junior Staff
- ZOOM Online: Development of Stability-Indicating HPLC Methods
- Pharmaceutical Manufacturing Support
- Pharmaceutical Product Development
- ZOOM Online: Tablet Compaction Analysis and how to improve your products
- ZOOM Online: Dissolution and the assessment of bioavailability/bioequivalence - 3.5 hours
- Pharmaceutical Granulation and Compression
- Introduction to the Formulation & Stabilisation of Protein and Peptide Drugs
- ZOOM Online: HPLC Troubleshooting
- Pharmaceutical Aerosols, Dry Powder Inhalation Systems and Nasal Delivery Devices
- Parenteral Products
- Latest Advances in the Stabilisation and Formulation of Protein and Peptide Drugs
- ZOOM Online: QbD and Lifecycle Management of Analytical Methods
- Developing Pharmaceutical Tablets for Low Cost Manufacturing
- Tablet Formulation Development - Formulation development in practice
- Stability Testing in Biological Product Development and Manufacturing
- Pharmaceutical R&D Support
