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  • GMP and Compliance
    • GMP Auditor Training for Quality Systems
    • OOS Investigations in a GMP Environment
    • GMP in Primary (API) Manufacturing
  • In-house Training Courses
    • Pharmaceutical Dissolution Testing - a 2 day course
    • 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
    • Oral Solid Dosage Manufacturing Technology
    • 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
  • Pharmaceutical Manufacturing Support
    • Training Course Programme 2020
    • Planning for Commercial Launch
    • Technology Transfer
  • Pharmaceutical Product Development
    • 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: 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
    • Tablet Formulation Development - Formulation development in practice
    • Stability Testing in Biological Product Development and Manufacturing
    • Hands-on Tablet Development including the principles of pre-formulation, formulation and process dev
    • ZOOM Online: Pharmaceutical Dissolution Testing - a 2 day Webinar
  • Pharmaceutical R&D Support
    • Stability Analysis for the Pharmaceutical Industry
    • Team building and decision-making

Showing 1–16 of 50 results

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    Chiral Analysis by Chromatography

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    Developing Pharmaceutical Tablets for Low Cost Manufacturing

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    Development and Manufacture of Effervescent Tablets

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    Gas chromatography: theory and practice for residual solvents testing

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    GMP Auditor Training for Quality Systems

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    GMP Auditor Training for Quality Systems

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    GMP in Primary (API) Manufacturing

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    Hands-on Tablet Development including the principles of pre-formulation, formulation and process dev

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    How to Audit API Manufacturers

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    In-house Training Courses

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    Integrated Tablet Formulation Development

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    Introduction to LC-MS for Pharma Industry

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    Introduction to Photostability

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    Introduction to Sterile Product Manufacture for New Starters and Junior Staff

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    Introduction to Sterile Product Manufacture for those with a cGMP basic understanding

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    Introduction to the Formulation & Stabilisation of Protein and Peptide Drugs

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