- GMP and Compliance
- Pharmaceutical Product Development
- Development and Manufacture of Effervescent Tablets
- HPLC Analytical Method Development and Validation
- Hands-on Tablet Development including the principles of pre-formulation, formulation and process dev
- 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
- Pharmaceutical Packaging - an introductory course
- Pharmacokinetics in Drug Development - an integrated approach
- Preformulation Studies for Tablet Development
- QbD and Lifecycle Management for Analytical Methods
- Quantitative Bioanalysis using LC-MS for Pharma Industry
- Stability Testing in Biological Product Development and Manufacturing
- Stability Testing in Pharmaceutical Development and Manufacture
- Tablet Formulation Development
- Tablet Process Development, Validation and the Application of QbD
- Technology Transfer
- Pharmaceutical Manufacturing Support
- Pharmaceutical R&D Support
- In-house Training Courses
Tablet Process Development, Validation and the Application of QbD
No Course Dates Currently Available
Overview
This interactive workshop provides up-to-date, relevant and detailed information on the impact of Quality by Design (QbD) on the Development and Validation of tablet manufacturing processes. It will also study the identification and evaluation of Critical Product Attributes and Critical Process Parameters for tablets, and their implications for process control. We develop new concepts including the use of risk and process matrices for risk management. The latest ICH and FDA guidance on Quality by Design and Process Development, published in 2009, will be comprehensively reviewed.Who Should Attend?
Tablet formulation and process development staff and those involved in managing process development and validation, and commissioning products into production. Regulatory Affairs staff preparing dossiers for tablet products. Quality Assurance personnel responsible for the design or implementation of tablet process validation protocols. Numbers will be limited to give participants the opportunity for thorough discussion of the issues to be covered by the programme and one on one consultation with speakers.Course Programme
Day 1: Morning - Product development
- The new regulatory landscape. Q8, Q9 and Q10 and their impact on product and process development
- Principles of Quality by Design and the product development process
- Linking material properties to formulation and processing behaviour
- Workshop session-Understanding Quality by Design
Afternoon-Mixing and blending
- Identifying potential Critical Process Parameters
- Use of Process Matrices in process development
- Unit processes 1 - Mixing and blending
- Assessing blend uniformity. Sampling problems and practice
- Workshop session-blend assessment practical. Effect of material properties on powder mixing behaviour
Day 2: Morning-Granulation-wet and dry
- Why granulation matters-good and bad
- Critical granulation process parameters and their impact
- Optimising granulation processes
- Workshop session-granulation practical. Effect of binder volume on product properties
Afternoon-Process Control and Process Analytical Technology (PAT)
- Principles of process control-feedback and feedforward
- Use of advanced techniques-limitations and applicability
- Case studies-what has been done? What is possible?
- Continuous processing
- Participants open forum and Question and Answer session.
NOTE
Wherever possible participants should bring practical problems and examples which can be reviewed on the course. The course will be highly participative and useful for people with or without experience.
Dress casual, you may get wet or dusty.








