Course Overview

    Overview

    Course Highlights

    Eligibility Criteria

    Benefits

    What Is Quality by Design and Why It Matters in QatarUntitledA Science-Based Route to Pharmaceutical Quality

    Quality by Design (QbD) Training in Qatar is a practical, non-certification programme that teaches pharmaceutical and biopharmaceutical professionals how to build quality into a product from the design stage rather than testing it in at the end. It is grounded in the ICH Q8(R2), Q9, Q10 and Q11 guidelines and the expectations of regulators such as the FDA and EMA. Across a focused one-day programme you learn to apply the Quality Target Product Profile (QTPP), Critical Quality Attributes (CQAs), risk assessment, Design of Experiments (DoE), the design space and the Control Strategy to real development work. Delivered by Invensis Learning in live virtual, classroom and corporate formats, it suits formulation scientists, process development engineers, analytical scientists, quality assurance professionals and regulatory affairs specialists. As Qatar builds its own pharmaceutical manufacturing base under Qatar National Vision 2030, employers increasingly expect science-based development skills. Start your QbD journey with Invensis Learning and put ICH-aligned quality thinking to work.

    What Is Quality by Design and Why It Matters in QatarA Science-Based Route to Pharmaceutical Quality

    Quality by Design (QbD) Training in Qatar is a practical, non-certification programme that teaches pharmaceutical and biopharmaceutical professionals how to build quality into a product from the design stage rather than testing it in at the end. It is grounded in the ICH Q8(R2), Q9, Q10 and Q11 guidelines and the expectations of regulators such as the FDA and EMA.

    Across a focused one-day programme you learn to apply the Quality Target Product Profile (QTPP), Critical Quality Attributes (CQAs), risk assessment, Design of Experiments (DoE), the design space and the Control Strategy to real development work. Delivered by Invensis Learning in live virtual, classroom and corporate formats, it suits formulation scientists, process development engineers, analytical scientists, quality assurance professionals and regulatory affairs specialists.

    As Qatar builds its own pharmaceutical manufacturing base under Qatar National Vision 2030, employers increasingly expect science-based development skills. Start your QbD journey with Invensis Learning and put ICH-aligned quality thinking to work.

    Certification Badge

    Key Highlightsof the Quality by Design Training Course

    End-to-End Skill Development

    • Structured Quality by Design training in the Qatar is designed to help learners understand QbD principles, regulatory frameworks, and pharmaceutical product development methodologies covered in the program
    • Course content aligned with current ICH Q8, Q9, and Q10 guideline expectations, real-world pharmaceutical quality requirements, and practical learning objectives for Qatar professionals delivered through a comprehensive Quality by Design training program
    • Real-world examples and scenario-based learning to help learners connect QbD concepts with everyday pharmaceutical development, manufacturing, and quality assurance situations
    • Guided learning support to help participants strengthen understanding, improve confidence, and apply QbD principles effectively across product development and manufacturing roles

    Structured Courseware and Learning Resources

    • Access to organized QbD course materials including QTPP definition worksheets, CQA and CMA identification templates, CPP mapping guides, and DoE reference cards designed to support step-by-step learning
    • Topic-wise learning resources, exercises, and knowledge checks to reinforce understanding of Design Space, control strategies, and risk assessment tools
    • Practice activities, assignments, and scenario-based exercises to help learners apply QbD concepts in realistic pharmaceutical product development and manufacturing quality situations
    • Supplementary learning aids such as risk assessment matrices, Design Space configuration worksheets, RTRT implementation checklists, and control strategy development guides

    Instructor-Led, Practical Learning Experience

    • Live interactive sessions delivered by experienced QbD practitioners with hands-on domain expertise across pharmaceutical, biotechnology, and manufacturing sectors
    • Real-world examples, case discussions, and applied QbD exercises to improve practical understanding of QTPP definition, CQA identification, DoE applications, and Design Space configuration
    • Opportunities to ask questions, clarify doubts, and participate in trainer-led discussions on risk assessment, CPP mapping, and regulatory compliance requirements
    • Training approach focused on helping learners apply QbD concepts confidently at work, not just complete the course content

    Flexible Learning Support in Qatar

    • Instructor-led training formats available for individual learners and corporate teams across the Qatar
    • Options include live virtual classroom training, onsite training, and customized group training depending on availability and organizational requirements
    • Learning support designed to help participants stay on track before, during, and after the Quality by Design training
    • Additional revision and post-training support may be available based on the selected course format

    Learn the Core Concepts Covered in the Course

    • Understand QbD fundamentals, background, key drivers, and the regulatory guidance documents including ICH Q8, Q9, and Q10 that shape modern pharmaceutical development
    • Learn how to define QTPP, identify CQAs, CMAs, and CPPs, apply DoE, configure Design Space, and develop control strategies based on the course curriculum
    • Explore practical use cases showing how QbD is applied in pharmaceutical, biotechnology, healthcare, and manufacturing environments
    • Build role-relevant knowledge of risk assessment and management, real-time release testing, and regulatory compliance that supports better quality decisions in product development

    Practice, Assessment, and Completion Support

    • Practice defining QTPP, identifying CQAs and CMAs, mapping CPPs, and applying DoE through exercises and scenario-based activities
    • Use assessments to identify knowledge gaps in QbD concepts and strengthen understanding of Design Space and control strategy development
    • Receive guidance from instructors to improve understanding of QbD tools and stay aligned with course objectives
    • Earn a course completion certificate after successfully meeting the training requirements

    Career and Workplace Application

    • Build practical QbD skills that can support career growth, role advancement, or improved pharmaceutical quality performance in the Qatar
    • Strengthen confidence in applying QTPP definition, CQA identification, DoE, Design Space, and risk management concepts to real-world product development challenges
    • Improve professional credibility through structured, skill-focused Quality by Design training recognized across Qatar pharmaceutical and manufacturing industries
    • Support enterprise capability building through Quality by Design corporate training for employees across pharmaceutical, biotechnology, healthcare, and manufacturing organizations.

    Quality by Design Training Eligibility in the QatarWho Can Enroll?

    • No formal prerequisites are required to enroll in the Quality by Design training program

    • Basic familiarity with quality assurance concepts is helpful but not mandatory for enrollment

    • Professionals from pharmaceutical, biotechnology, healthcare, and manufacturing industries are well-suited for this training

    • Individuals and corporate teams seeking to build QbD knowledge and apply regulatory-aligned product development principles are eligible to enroll

    • Learners with backgrounds in quality, regulatory affairs, process engineering, and production management will find the content directly applicable to their roles

    Why Quality by Design Skills Are Worth BuildingOutcomes for You and Your Team

    For Individuals

    For Individuals

    Quality by Design training gives pharmaceutical professionals a practical, science-based way to develop products and processes. You learn to define what a product must achieve, identify what is critical to quality, and control it through understanding rather than end-product testing. Whether you work in formulation, analytical development, process engineering, quality assurance or regulatory affairs, the training builds capability you can apply to live projects straight away.

    If you want to move beyond routine testing and into designing robust, compliant processes, QbD is a clear step forward. You gain ICH-aligned tools, hands-on practice and a structured approach that pharmaceutical employers across Qatar increasingly value.

    • Build quality into products from the design stage instead of testing it in at the end
    • Apply the full QbD toolkit: QTPP, CQAs, risk assessment, DoE, design space and Control Strategy
    • Speak the ICH Q8 to Q11 language that regulators and CMC teams expect
    • Replace slow trial-and-error development with structured, science-based decisions
    • Lead risk assessments using Ishikawa diagrams and FMEA with RPN prioritisation
    • Prepare development evidence that supports CTD regulatory submissions
    • Strengthen your profile as Qatar expands local pharmaceutical manufacturing
    • Move from following procedures to designing robust, reliable processes
    For Organizations

    For Organizations

    Quality by Design group training helps pharmaceutical and biopharmaceutical organisations embed science-based development across their teams. Delivered onsite or live virtual, it equips cross-functional groups with a common approach to the QTPP, CQAs, risk assessment, DoE and Control Strategy. For organisations scaling local manufacturing or preparing regulatory submissions, this builds capability that reduces risk and improves consistency.

    If your teams still rely on trial-and-error development and end-product testing, QbD training creates a shared, ICH-aligned framework. Groups gain a standardised way to design quality in and defend it to regulators.

    • Build a shared QbD language across formulation, analytical, process, QA and regulatory teams
    • Reduce manufacturing deviations through stronger process understanding
    • Cut the post-approval change burden by defining a robust design space
    • Strengthen CTD submissions with structured pharmaceutical development evidence
    • Standardise risk assessment and DoE practice across development projects
    • Support Qatar National Vision 2030 goals for local pharmaceutical manufacturing
    • Train a cross-functional team together on your own live products
    • Improve product consistency and regulatory confidence

    Where QbD Skills Take Your CareerRoles and Demand in Qatar Pharma

    Quality by Design skills are becoming a differentiator for pharmaceutical professionals in Qatar as the country builds its own manufacturing base under Qatar National Vision 2030. Local manufacturers, biopharma firms and regulatory teams increasingly want people who can apply ICH-aligned development rather than test quality in at the end. Demand spans formulation, analytical, process, quality assurance and regulatory affairs roles, and here is what the market shows.

    $4.2bn

    Qatar pharmaceutical market, 2025

    projected $10.6bn by 2034

    QAR 245,300

    QA Manager salary, Qatar

    median, PayScale 2026

    QAR 392,300

    Pharma research scientist, Doha

    average, WorldSalaries

    ~11%

    Pharma market growth rate

    CAGR, 2025-2034

    SECTORS HIRING

    • —Local Pharmaceutical Manufacturing (QLife Pharma, QPI, Qatar Pharma)
    • —Biopharmaceutical and Advanced Therapies
    • —Hospital and Government Pharmacy (Hamad Medical Corporation)
    • —Regulatory Affairs and CMC
    • —Contract Development and Manufacturing
    • —Academic and Clinical Research

    GROWTH TRENDS

    • —Qatar pharma market near $4.2bn in 2025 and rising fast
    • —Qatar National Vision 2030 driving local drug manufacturing
    • —New QPI plant and biosimilars pipeline expanding by 2028
    • —Shift toward biologics, oncology and speciality medicines
    • —Reduced import dependency lifting demand for QbD skills
    • —Regulators expecting ICH-aligned development evidence

    Sources: PayScale, WorldSalaries, Paylab (Qatar) 2025-2026; Bionixus, Gulf Times, Invest Qatar (pharma market); Qatar National Vision 2030.

    What Is Driving Demand for QbD Skills in Qatar

    Rapid Local Manufacturing Growth

    Qatar is building its own pharmaceutical manufacturing base under Qatar National Vision 2030 to cut its roughly 95% import dependency, and new plants need staff who can design quality in from the start.

    QbD builds design-in-quality skills

    Rising Regulatory Expectations

    Regulators including the FDA and EMA increasingly expect ICH Q8 to Q11 QbD evidence in submissions, so Qatar's manufacturers and CMC teams need people who can produce it.

    QbD builds ICH-aligned evidence skills

    Shift Toward Biologics and Advanced Therapies

    Qatar's market is moving toward biologics, oncology and speciality medicines, which demand the deep process understanding that QbD and Design of Experiments provide.

    QbD builds process understanding skills

    Scarce Science-Based Development Talent

    The region has many QC and testing staff but few professionals fluent in QTPP, CQA identification and design space definition, making applied QbD skills genuinely rare.

    QbD makes your profile stand out

    Pressure to Reduce Deviations and Rework

    Manufacturers under cost and supply pressure need robust processes that limit batch failures, which is exactly what a well-built, risk-based Control Strategy delivers.

    QbD builds Control Strategy skills

    Complex Post-Approval Change Burden

    Without a defined design space, every change triggers regulatory work; QbD gives teams the operating flexibility that ICH Q12 lifecycle management rewards.

    QbD builds design space and lifecycle skills

    Sources: Bionixus, Gulf Times, Invest Qatar, BioSpace (pharma market) 2025-2026; ICH Q8 to Q12 guidelines; Qatar National Vision 2030.

    Quality by Design is more than a concept. It is the capability Qatar's pharmaceutical sector needs to design quality in and satisfy regulators. Build these skills and lead development that stands up to scrutiny. Start today.

    Your Qatar QbD Skill Transformation

    From Testing Quality in to Designing It In,

    And Where QbD Skills Take You

    Qatar's pharmaceutical sector is expanding local manufacturing and moving toward biologics and speciality medicines, and employers increasingly separate professionals who can design quality in from those who only test it. Here is the shift QbD training delivers.

    Today

    You rely on end-product testing to catch quality problems late

    After QbD

    You design quality in from the QTPP stage and prevent problems early

    Today

    Development runs on trial and error, one factor at a time

    After QbD

    You use DoE and the design space to understand processes systematically

    Today

    Regulatory submissions feel like a scramble for justification

    After QbD

    You produce ICH-aligned evidence that supports a confident CTD submission

    You master QbD

    Before

    Quality seen as a QC checkpoint at the end of the line

    Now you have

    A science-based approach that builds quality into the product

    Before

    Limited fluency in the ICH Q8 to Q11 guidelines

    Now you have

    Command of the framework regulators and CMC teams expect

    Before

    Skills tied to one task or a single test method

    Now you have

    Cross-functional capability valued across Qatar's pharma sector

    Before

    Change control means constant post-approval paperwork

    Now you have

    A design space that gives your team room to operate

    "Quality cannot be tested into products; it should be built in by design. The teams that internalise this are the ones regulators come to trust."

    Join 50,000+ professionals who trained with Invensis Learning and put it into practice.

    Sources: PayScale, WorldSalaries (Qatar) 2025-2026; Invest Qatar, Gulf Times (pharma market).

    Module 1: Introduction to QbD

    • Background and key drivers that led to the adoption of Quality by Design in pharmaceutical development
    • Regulatory guidance documents including ICH Q8, Q9, and Q10 that define the QbD framework
    • QbD development process flow from concept and design through to manufacturing and regulatory submission

    Module 2: QbD Tools and Techniques

    • Risk management principles and tools used to identify, assess, and control quality risks in product development
    • Design of Experiments (DoE): fundamentals, design types, and how DoE is used to understand process variability
    • Design Space definition and control strategies: how boundaries are established and maintained throughout the product lifecycle

    Module 3: Industry and Regulatory Perspective

    • Regulatory framework for QbD including agency expectations from the FDA, EMA, and ICH guidelines
    • Implementation challenges organizations face when transitioning from traditional to QbD-based development approaches
    • Real-world industry examples demonstrating how pharmaceutical and biotechnology organizations have adopted QbD

    Module 4: Quality Target Product Profile (QTPP)

    • Definition of the Quality Target Product Profile and its role in guiding QbD-based product development decisions
    • How QTPP links patient needs and regulatory requirements to specific product quality attributes and design objectives
    • Practical steps for defining a QTPP for pharmaceutical and biotechnology products

    Module 5: Critical Quality Attributes, Critical Material Attributes, and Critical Process Parameters

    • Identifying Critical Quality Attributes (CQAs): what they are, how to define them, and why they are central to QbD
    • Critical Material Attributes (CMAs): how raw material properties influence product quality and must be controlled
    • Critical Process Parameters (CPPs): identifying process parameters that impact CQAs and require monitoring and control

    Module 6: Statistical Design of Experiments

    • Fundamentals of statistical DoE including full factorial, fractional factorial, and response surface methodologies
    • Applications of DoE in pharmaceutical process development and optimization
    • Interpreting DoE results to establish design space boundaries and process understanding

    Module 7: Design Space and Process Control

    • Design Space concept: defining the multidimensional combination of input variables and process parameters that provide quality assurance
    • Implementation of Design Space within regulatory submissions and manufacturing control strategies
    • Continuous process verification and how Design Space supports process control across the product lifecycle

    Module 8: Risk Assessment and Management

    • Risk assessment methodologies used in QbD including FMEA, Ishikawa diagrams, and risk ranking tools
    • Applying risk management principles to product development decisions, process design, and control strategy development
    • Linking risk assessment outcomes to Design Space boundaries and CQA control strategies

    Module 9: Real-time Release Testing (RTRT)

    • RTRT concept: replacing end-product testing with in-process monitoring and real-time quality assurance
    • Regulatory requirements and industry expectations for RTRT implementation in pharmaceutical manufacturing
    • Practical considerations for implementing RTRT as part of a QbD-based control strategy

    Module 10: Case Studies and Practical Applications

    • Pharmaceutical and biotechnology case studies demonstrating end-to-end QbD implementation from QTPP to RTRT
    • Practical group exercises and scenario analysis applying QbD tools including QTPP definition, CQA identification, DoE, and risk assessment
    • Lessons learned and best practices from real QbD projects in pharmaceutical, biotechnology, and manufacturing environments

    Course Curriculumof the Quality by Design Training

    The online Quality by Design training course curriculum in the Qatar is structured across ten modules, taking learners from foundational QbD background and regulatory guidance through to real-world case studies and practical applications in pharmaceutical, biotechnology, and manufacturing environments.

    • Background and key drivers that led to the adoption of Quality by Design in pharmaceutical development
    • Regulatory guidance documents including ICH Q8, Q9, and Q10 that define the QbD framework
    • QbD development process flow from concept and design through to manufacturing and regulatory submission

    Shifts your thinking from testing quality in at the end to designing it in from the start.

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    Apply the Full Quality by Design ToolkitQTPP, DoE and the Design Space in Practice

    This Quality by Design programme turns ICH theory into practical capability. By the end, you can apply QbD tools to real pharmaceutical development scenarios and lead the workshops that produce them.

    Build a Quality Target Product Profile

    In Quality by Design training you learn to construct a Quality Target Product Profile (QTPP) from clinical and patient needs, defining exactly what a product must achieve for quality, safety and efficacy before development begins.

    Identify and Classify Critical Quality Attributes

    Determine which physical, chemical and biological properties are critical to product quality, and separate true CQAs from non-critical attributes for both small molecules and biologics.

    Run Risk Assessments with Ishikawa and FMEA

    Map potential sources of variation with fishbone diagrams and prioritise CMA and CPP risks using FMEA and Risk Priority Numbers, so development effort targets the highest-impact variables.

    Design and Interpret DoE Studies

    Use Design of Experiments to study multiple factors at once, moving beyond one-factor-at-a-time testing to quantify how process parameters and material attributes affect your critical quality attributes.

    Define the Design Space and Operating Ranges

    Derive a design space from DoE results and set Normal Operating Ranges and Proven Acceptable Ranges, understanding the edge of failure and the regulatory flexibility a design space provides.

    Build a PAT-Enabled Control Strategy

    Develop a risk-proportionate Control Strategy using material controls, in-process controls, end-product testing and Process Analytical Technology, and document it for a CTD regulatory submission.

    Who Should TakeQuality by Design Training in Qatar?

    Process Engineers

    QC Analysts

    Engineering Teams

    Technical Staff

    Production Managers

    Distribution Managers

    Regulatory Affairs Specialists

    Quality Assurance Professionals

    Who Can Take This Certification Training

    Quality by Design Training Modesfor Professionals and Teams

    We offer flexible training formats designed to suit different learning preferences, schedules, and professional goals. Whether you prefer self-paced learning or a structured, corporate, instructor-led experience, choose the option that best supports your skill development journey with the best Quality by Design online training options.

    Quality by Design Live Virtual Training

    • Live online instructor-led sessions

    • Interactive discussions and virtual activities

    • Expert guidance from experienced trainers

    • Practice assessments and revision support

    • Dedicated Q&A sessions for concept clarification

    • Fixed schedules for accountability and momentum

    • Small batch sizes for personalized attention

    • Access from any location with internet connectivity

    QAR 1580

    Attend fully interactive weekday Quality by Design training sessions from anywhere while benefiting from real-time instructor guidance and collaborative learning experiences.

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    Best For: Professionals seeking the flexibility of online learning without compromising on live instructor interaction.

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    Quality by Design Classroom Training

    • Instructor-led classroom sessions

    • Interactive discussions and group activities

    • Real-world examples and practical exercises

    • Structured learning with fixed schedules

    • Opportunities for peer networking and collaboration

    • Practice assessments and knowledge checks

    • Dedicated Q&A and concept clarification

    • Immediate trainer feedback and support

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    Learn through face-to-face sessions led by experienced instructors in a collaborative classroom environment. This classroom Quality by Design training combines expert guidance, peer interaction, and hands-on activities to create an engaging learning experience.

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    Best For: Learners who prefer in-person interaction, structured schedules, and collaborative learning experiences.

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    Quality by Design Corporate Group Training

    • Customized training aligned to organizational goals

    • Flexible delivery: onsite, virtual, hybrid, or blended

    • Scheduling tailored to business availability

    • Role-based examples and industry-relevant discussions

    • Progress tracking and learner assessments where applicable

    • Dedicated coordination and administrative support

    • Consistent learning experiences across teams

    • Scalable delivery for local, regional, or global workforces

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    Designed for organizations that want to build capabilities at scale, standardize knowledge, and support workforce development through customized team learning initiatives.

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    Best For: Organizations looking to upskill employees, address capability gaps, and deliver consistent training across teams.

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    Quality by Design Focused 1-to-1 Training

    • One-to-one instructor attention

    • Customized learning plans and objectives

    • Flexible scheduling based on availability

    • Personalized feedback and coaching

    • Additional focus on challenging topics

    • Targeted practice and revision support

    • Faster clarification of questions and concepts

    • Learning pace is adapted to individual needs

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    Receive personalized instruction tailored to your goals, pace, and learning requirements through dedicated sessions from our trusted Quality by Design training company.

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    Best For: Professionals seeking personalized guidance, accelerated learning, or focused support to achieve specific outcomes.

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    Quality by Design Live Virtual Training

    Quality by Design Live Virtual Training

    Live online instructor-led sessions

    Interactive discussions and virtual activities

    Expert guidance from experienced trainers

    Practice assessments and revision support

    Dedicated Q&A sessions for concept clarification

    Fixed schedules for accountability and momentum

    Small batch sizes for personalized attention

    Access from any location with internet connectivity

    Starts from

    QAR 1580

    Please Note:Attend fully interactive weekday Quality by Design training sessions from anywhere while benefiting from real-time instructor guidance and collaborative learning experiences.

    Best For: Professionals seeking the flexibility of online learning without compromising on live instructor interaction.

    Loading schedules…

    Quality by Design Training in Qatar with Invensis LearningExpert-Led Training You Can Trust

    Invensis Learning is a trusted Quality by Design training company in Qatar, delivering instructor-led training for pharmaceutical professionals and organisations across Qatar. Our programmes combine experienced practitioner trainers, hands-on QbD tool exercises and flexible delivery designed around practical, on-the-job application. Whether you enrol as an individual or arrange corporate training for a cross-functional team, we back the learning with ISO-certified quality standards, structured courseware and dedicated support, so your people leave able to apply ICH-aligned QbD to live development work.

    • ISO 9001:2015 certified training provider with quality management you can trust
    • Experienced, practitioner trainers with real pharmaceutical and quality expertise
    • Flexible delivery: live online, classroom, onsite and customised corporate formats
    • Hands-on QbD tool exercises using realistic pharmaceutical development scenarios
    • Course completion certificate from Invensis Learning on finishing the programme
    • ISO 27001:2022 certified for information security and data protection
    • Global training network with local support across Qatar and the wider Gulf
    • Dedicated learner support before, during and after training

    500+

    Corporate Clients

    15+

    Years of Training Excellence

    24/7

    Learner Support

    50+

    Industries Served

    ISO 9001:2015 Certified

    ISO 9001:2015 Certified

    ISO 27001:2022 Certified

    ISO 27001:2022 Certified

    Secure SSL Encryption

    Secure SSL Encryption

    Leaders in Training industry for 12+ years

    Leaders in Training industry for 12+ years

    Over 5000 five star reviews

    Over 5000 five star reviews

    Level AA conformance, W3C WCAG 2.2

    Level AA conformance, W3C WCAG 2.2

    Quality by Design Training Locations in QatarAll our classroom training is now available online at your convenience

    Quality by Design in Qatar

    Sheraton Grand Doha Resort & Convention Hotel, Qatar

    Quality by Design in Qatar

    Sharq Village and Resort, Ras Abu Aboud Street, Al Mina District, Sharq - Al Khalifat, Doha, Qatar

    corporate banner

    Corporate QbD Training for TeamsUpskill Qatar's Pharma Workforce

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    • Customised QbD training for pharmaceutical and biopharmaceutical teams
    • Flexible onsite, live virtual, hybrid or blended delivery across Qatar
    • Apply QbD tools to your own live products during the session
    • Build a shared QTPP, CQA, DoE and Control Strategy language across teams
    • Experienced trainers with pharmaceutical quality and development expertise
    • Scheduling aligned to your team's availability and project timelines
    • Dedicated coordination and learner support for corporate groups

    Pharmaceutical Organisations in Qatar

    QLife PharmaQatar Pharmaceutical IndustriesQatar PharmaAnabionHamad Medical CorporationSidra Medicine

    What Our Learners Say

    Untitled

    A Practical Shift in How I Develop Products

    "The training completely changed how I approach formulation. I now start with a QTPP and map my critical quality attributes before touching the lab. Building a design space from DoE results is something I use on every project now."

    Aisha Al-Sulaiti

    Formulation Scientist

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    0/0

    Clear, Hands-On and Job-Ready

    "As an analytical scientist I finally understand where my methods fit in the bigger QbD picture. The sessions on risk assessment with FMEA and on Process Analytical Technology were clear, hands-on and immediately useful at work."

    Mohammed Rahman

    Analytical Scientist

    Untitled

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    Connected the Dots for Regulatory Work

    "The best part for me was learning how QbD outputs map into a CTD submission. The QTPP, risk assessment and Control Strategy now make sense as one story I can defend to regulators. Strong, well-structured training."

    Priya Nair

    Regulatory Affairs Specialist

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    Gave Our Teams a Shared QbD Language

    "We ran this as an onsite programme for our development and QA teams. Everyone now shares the same language around CQAs, design space and Control Strategy, which has already reduced back-and-forth on our current projects."

    Khalid Al-Mannai

    Quality Assurance Manager, Pharmaceutical Manufacturing

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    Tailored Corporate Training That Delivered

    "As we scale local manufacturing, we needed our people to think in terms of designing quality in, not testing it later. The corporate training was tailored to our products and the trainer's real-world experience made it land with the team."

    Sara Hassan

    Head of Development, Biopharmaceuticals

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    Frequently Asked QuestionsHere's everything you may ask...

    Quality by Design training is a one-day, non-certification programme that teaches a science-based approach to pharmaceutical development. You learn to build quality into a product from the design stage using ICH Q8 to Q11 tools such as the QTPP, CQAs, risk assessment, DoE, design space and Control Strategy, rather than testing quality in at the end.

    General

    What is Quality by Design (QbD) training?

    Quality by Design training is a one-day, non-certification programme that teaches a science-based approach to pharmaceutical development. You learn to build quality into a product from the design stage using ICH Q8 to Q11 tools such as the QTPP, CQAs, risk assessment, DoE, design space and Control Strategy, rather than testing quality in at the end.

    Is QbD training worth it for professionals in Qatar?

    Yes. As Qatar expands local pharmaceutical manufacturing under Qatar National Vision 2030, employers increasingly want people who can apply ICH-aligned development. QbD skills apply across formulation, analytical, process, quality and regulatory roles, and are immediately usable on live projects.

    Which framework and guidelines does the training follow?

    The training is grounded in the ICH Q8(R2) Pharmaceutical Development, Q9 Quality Risk Management, Q10 Pharmaceutical Quality System and Q11 drug substance guidelines, along with FDA and EMA expectations. These form the recognised basis of modern QbD practice.

    Who should attend QbD training?

    The training suits formulation scientists, process development engineers, analytical scientists, quality assurance professionals, regulatory affairs and CMC specialists, and manufacturing technical managers in pharmaceutical, biopharmaceutical, API and medical device organisations who want to apply QbD in their work.

    Do I receive a certificate after the training?

    You receive a course completion certificate from Invensis Learning. This is a non-certification skills course, so there is no external credential or examination; the focus is practical QbD capability you can apply straight away.

    Pricing

    How much does QbD training cost in Qatar?

    Pricing varies by delivery format (live virtual, classroom or corporate) and group size. For individual and group pricing in Qatari riyals, request a quote and a learning advisor will share current options. Ask about corporate rates when training a team.

    What is included in the course fee?

    The fee typically includes instructor-led training across all QbD modules, structured courseware and learning resources, hands-on QbD tool exercises, pharmaceutical case studies and a course completion certificate. Request a quote for a full breakdown.

    Do you offer corporate or group pricing?

    Yes. We offer corporate group training with customised schedules and group-based pricing for pharmaceutical and biopharmaceutical teams in Qatar. Contact us for a tailored quote for your organisation.

    Are there payment or instalment options?

    We accept major cards and bank transfers, and offer instalment options on selected plans. Speak with a learning advisor to choose the option that suits you.

    Is there any exam or certification fee?

    No. This is a non-certification course, so there is no examination or external certification fee. The fee covers the training, courseware, hands-on exercises and your course completion certificate.

    Assessment

    Is there an exam for QbD training?

    No. Quality by Design training is a non-certification course with no examination. Learning is reinforced through hands-on QbD tool exercises, pharmaceutical case studies and group discussion during the programme.

    How is learning reinforced during the training?

    There is no formal assessment. You apply QbD tools to realistic development scenarios throughout the day, constructing a QTPP, identifying CQAs, running a risk assessment and interpreting a design space, so you practise every tool as you learn it.

    What will I be able to do after the training?

    You will be able to construct a QTPP, identify and classify CQAs, run risk assessments with Ishikawa diagrams and FMEA, plan and interpret DoE studies, define a design space with operating ranges, and build a Control Strategy for regulatory submission.

    Do I need prior QbD knowledge to attend?

    No. There are no formal prerequisites. Familiarity with pharmaceutical development or GMP is helpful but not required, as the training introduces QbD from first principles in a pharmaceutical development context.

    Will the training help with regulatory submissions?

    Yes. You learn how QbD outputs, the QTPP, CQAs, risk assessment, design space and Control Strategy, form Section 3.2.P.2 of a CTD submission, so you can structure development evidence for regulators such as the FDA and EMA.

    Course Content

    What topics does the QbD training cover?

    The programme covers QbD principles and the ICH regulatory framework, the QTPP and CQAs, risk assessment, Design of Experiments and design space definition, Process Analytical Technology and Control Strategy, and QbD in practice through case studies and lifecycle management.

    Does the training cover both small molecules and biologics?

    Yes. The training covers QbD principles for small molecule drug products such as tablets and injectables, and for biopharmaceuticals such as monoclonal antibodies and biosimilars, with case study examples from both.

    Is Design of Experiments (DoE) covered?

    Yes. The training explains how to design, run and interpret DoE studies within QbD, including screening and response surface designs, and how DoE results define the design space and operating ranges.

    Does it cover Process Analytical Technology (PAT)?

    Yes. You learn how PAT tools such as NIR and Raman spectroscopy enable real-time monitoring, how real-time release testing works, and how PAT fits into a risk-based Control Strategy.

    What learning materials are provided?

    You receive structured courseware covering all QbD modules, hands-on tool exercises, realistic pharmaceutical development case studies and reference materials aligned to the ICH Q8 to Q11 guidelines.

    Enrolment

    How do I enrol in QbD training in Qatar?

    You can enrol through the Invensis Learning website. Choose your preferred format, complete payment and you will receive access to schedules, courseware and learning resources. Talk to a learning advisor to pick the right batch for you.

    What delivery formats are available?

    QbD training is available online as live virtual instructor-led sessions, in classroom, onsite, and as customised corporate training, so you can choose the format that fits your schedule and your team.

    How long is the training?

    The programme runs for one day (8 hours) and covers all QbD modules, from principles and the ICH framework through the QTPP, CQAs, risk assessment, DoE, design space, PAT and Control Strategy, with hands-on exercises throughout.

    Can I arrange training for my team in Qatar?

    Yes. We deliver corporate onsite and live virtual training for pharmaceutical and biopharmaceutical teams across Qatar, tailored to your products so participants can apply QbD tools to live development projects. Request corporate training to plan a session.

    Can I reschedule my enrolment to another batch?

    Yes. Flexi options let you reschedule or transfer to another batch. Contact our support team to arrange this and see upcoming schedules.