(DOE) Design of Experiement in Pharmaceutical Development
What you'll learn
- Pharmacy Graduates Students
- Pharmacy PG Diploma
- Diploma Pharmacy Students
- Research scientists
- Pharma Professional
- Pharma R & D Students
- Research Scholars
- Project Interns
- Pharmaceutical product Developer
- Pharmaceutical industry Researcher, formulators
- All Graduates / Post-Graduates
- Bachelor of pharmacy
If you are looking for DOE for Pharmaceutical Development course so this is for you with cheap cost.
To learn design space creation and over all design of experiment, you also need some knowledge of Risk assessment and critical parameter assessment. There are plenty of books available for this topic but its better to go through research papers related to specific field of interest. That will give you a better perspective of it.
Alos there are plenty of softwares like JMP and sigma plot which offer a free trial where you can learn to creat Design space with simple clicks.
At the beginning of the twentieth century, Sir Ronald Fisher introduced the concept of applying statistical analysis during the planning stages of research rather than at the end of experimentation. When statistical thinking is applied from the design phase, it enables to build quality into the product, by adopting Deming's profound knowledge approach, comprising system thinking, variation understanding, theory of knowledge, and psychology.
The pharmaceutical industry was late in adopting these paradigms, compared to other sectors. It heavily focused on blockbuster drugs, while formulation development was mainly performed by One Factor At a Time (OFAT) studies, rather than implementing Quality by Design (QbD) and modern engineering-based manufacturing methodologies. Among various mathematical modeling approaches, Design of Experiments (DoE) is extensively used for the implementation of QbD in both research and industrial settings.
In QbD, product and process understanding is the key enabler of assuring quality in the final product. Knowledge is achieved by establishing models correlating the inputs with the outputs of the process. The mathematical relationships of the Critical Process Parameters (CPPs) and Material Attributes (CMAs) with the Critical Quality Attributes (CQAs) define the design space.
Consequently, process understanding is well assured and rationally leads to a final product meeting the Quality Target Product Profile (QTPP). This review illustrates the principles of quality theory through the work of major contributors, the evolution of the QbD approach and the statistical toolset for its implementation. As such, DoE is presented in detail since it represents the first choice for rational pharmaceutical development.
Keywords: Experimental design; design space; factorial designs; mixture designs; pharmaceutical development; process knowledge; statistical thinking.
The objective of Design of Experiments Training is to provide participants with the analytical tools and methods necessary to:
Plan and conduct experiments in an effective and efficient manner
Identify and interpret significant factor effects and 2-factor interactions
Develop predictive models to explain process/product behavior
Check models for validity
Apply very efficient fractional factorial designs in screening experiments
Handle variable, proportion, and variance responses
Avoid common misapplications of DOE in practice
Participants gain a solid understanding of important concepts and methods to develop predictive models that allow the optimization of product designs or manufacturing processes. Many practical examples are presented to illustrate the application of technical concepts. Participants also get a chance to apply their knowledge by designing an experiment, analyzing the results, and utilizing the model(s) to develop optimal solutions. Minitab or other statistical software is utilized in the class.
CONTENT of course
Introduction to Experimental Design
What is DOE?
When to use DOE
Common Pitfalls in DOE
A Guide to Experimentation
Planning an Experiment
Implementing an Experiment
Analyzing an Experiment
Two Level Factorial Designs
Design Matrix and Calculation Matrix
Calculation of Main & Interaction Effects
Using Center Points
Identifying Significant Effects
Variable & Attribute Responses
Describing Insignificant Location Effects
Determining which effects are statistically significant
Analyzing Replicated and Non-replicated Designs
Developing Mathematical Models
Developing First Order Models
Residuals /Model Validation
Fractional Factorial Designs (Screening)
Structure of the Designs
Identifying an “Optimal” Fraction
Analysis of Fractional Factorials
Proportion & Variance Responses
Sample Sizes for Proportion Response
Identifying Significant Proportion Effects
Handling Variance Responses
Intro to Response Surface Designs
Central Composite Designs
Optimizing several characteristics simultaneously
DOE Projects (Project Teams)
Planning the DOE(s)
Recently, DoE has been used in the rational development and optimization of analytical methods. Culture media composition, mobile phase composition, flow rate, time of incubation are examples of input factors (independent variables) that may the screened and optimized using DoE.
Look for course description .... look for see you in the class....
Who this course is for:
- Research & Development
- Bachelor of Pharmacy Students
- Master of Pharmacy Students
- Bachelors of Science
- Master of Science
- Career in Research and Development
- Pharmacy Students
- Pharma industry Professionals
I Am Mahesh Pratapwar.
I am Pharma Professional, having skill of Pharmaceutical Product development and Complying with Regulatory Specifications for Pharmaceutical products according to guidelines of US/Europe/CDSCO.
I have completed M.Pharm (P.Ceutics).
Work experience more than 6 years in Pharma Industry.
Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. ... Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug.
Skills: Formulation & Development, Stability studies, QbD, OSD, Oral Liquids, Topical/Derma, DRA, CTD & eCTD, Plant exposure, Bioequivalence, DoE, etc...
Published more than 3 Research and review articles in high impact journals.
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