Your Expert Trainer
He has 50 years of industry experience and is a leading consultant and expert in the areas of cGMP, Quality by Design, Quality Management, Regulatory Compliance & Affairs for the Pharmaceutical..
Highly Rated Pharma QBD Masterclass Comes to YOU LIVE ONLINE!
Quality by Design (QbD) brings a systematic approach to drug development that will ensure quality by applying analytical and risk-management methodologies to the design, manufacturing and development of new medications. At its core, the approach can design quality into workflows up front.
QbD provides a robust framework for the design and implementation of processes that achieve a consistent level of quality and meet the pre-defined standards, whilst ensuring minimal risks and maximum control in the manufacturing, drug product and process development. Applying QBD to Drug Development Programs has huge advantages and it can ensure a robust manufacturing process that produces high quality and consistent drug products. As regulatory authorities demand manufacturers design quality into products at every stage of development and manufacturing, the use of QbD will become increasingly critical and it’s important you get this right.
All these and more will be covered in this practical, case-study driven and comprehensive Pharma QBD Masterclass, conducted LIVE ONLINE this coming 22-24 February 2021! Don't miss it!
10 Key Reasons Why This Pharma Quality By Design Masterclass is a MUST-ATTEND EVENT:
- Learn how you can develop an effective roadmap to implementing Quality By Design Principles in your Manufacturing & Drug Development Process
- Improve your understanding of quality risk management and assessment including the different risk control methodologies
- Enhance your robustness of your manufacturing processes to facilitate continuous improvement and improved product quality & availability throughout a product’s lifecycle
- Find out how you can use analytical method development and validation
- Learn how to use statistical methods and data analysis in Pharma QBD
- Build up your knowledge on Process Control Strategy Planning & Design
- In depth analysis of how Process Analytical Technology can be used as a key tool for effective QBD implementation
- Gain understanding on regulatory initiatives, approaches, requirements and expectations whilst realizing Process Design
- Improve your knowledge on the reporting and documentation of drug product development results
- Hear global case studies on how QBD can be efficiently applied to pharmaceutical development and manufacturing
Who Should Attend:
Tailor-made specifically for pharmaceutical and biotechnology companies and from the following divisions:
- Product Development
- Process Development
- Process Design
- Process Validation
- Manufacturing Process
- Design Control
- Contract Manufacturing
- Quality Assurance
- Regulatory Compliance
- Regulatory Affairs
- Scientific Affairs/Chief Scientific Officers
- R&D
Like More Information?
Email us today at enquiry@equip-global.com!