Quality by Design Training in Portugal

Build It in, Don't Test It In

Built for formulation scientists, process and analytical scientists, QA and regulatory affairs professionals in Portugal's growing pharmaceutical and CDMO sector. This instructor-led programme, delivered by an experienced Quality by Design training company, shows you how to design quality into products from the outset using the ICH Q8 to Q11 framework, QTPP, CQAs, risk assessment, Design of Experiments and control strategy.

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What Is Quality by Design and Why Pharma Relies on ItThe Modern Standard in Pharmaceutical Development

Quality by Design (QbD) is a systematic, science-based approach to pharmaceutical development that builds quality into a product from the design stage rather than testing it in at the end. This Quality by Design training in Portugal introduces the QbD approach and the ICH guidelines that underpin it, so you can apply the method with confidence on real development projects.

QbD is mandated by ICH Q8(R2) Pharmaceutical Development, Q9 Quality Risk Management, Q10 Pharmaceutical Quality System and Q11, and is increasingly expected by regulators including the FDA, the EMA and, locally, INFARMED. Across one practical day you learn how to move from a Quality Target Product Profile (QTPP) and Critical Quality Attributes (CQAs) through risk assessment, Design of Experiments and the design space to a robust control strategy.

Whether you work in formulation, process development, analytical science, quality assurance or regulatory affairs, the programme gives you tools you can use immediately across Portugal's pharmaceutical, biopharmaceutical and CDMO organisations. Start building quality in by design with Invensis Learning.

Key Highlightsof the Quality by Design Training Course

End-to-End Skill Development

Structured Quality by Design training in the Portugal 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 Portugal 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 Portugal

Instructor-led training formats available for individual learners and corporate teams across the Portugal
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 Portugal
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 Portugal 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 PortugalWho 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

Skills You Can Put to Work Straight AwayReal Capability, Not Just Theory

For Individuals

This QbD training helps pharmaceutical professionals design quality into products from the outset instead of relying on end-product testing. It suits formulation and analytical scientists, process development engineers, QA specialists and regulatory affairs professionals who want a practical, applicable method. Whether you are moving from empirical development, preparing CMC submissions, or working in a CDMO delivering for global clients, the training builds capability you can apply the very next day.

If you want to work the way modern regulators and international clients expect, QbD is a clear step forward. You gain hands-on tools, worked pharmaceutical and biologic examples, and a structured method that connects development science to consistent product quality.

Replace trial-and-error development with a structured, science-based QbD method
Build a QTPP and identify Critical Quality Attributes with confidence
Lead risk assessments using Ishikawa diagrams and FMEA to focus your effort
Plan a Design of Experiments and interpret a design space with NOR and PAR
Turn QbD outputs into a defensible control strategy for manufacturing
Speak the ICH Q8 to Q11 language that regulators and CDMO clients expect
Strengthen your standing for QA, regulatory and technical roles in Portugal

For Organizations

QbD group training helps organisations build development and quality capability by equipping cross-functional teams with a common, ICH-aligned method. The training can be delivered for R&D, quality and regulatory groups together. For pharmaceutical, biopharmaceutical and CDMO organisations that want consistent, right-first-time development, this training provides a scalable, flexible solution.

If your teams develop products through trial and error and firefight quality at the end, QbD training creates a shared, systematic approach. Cross-functional teams gain a common way to define quality targets, assess risk, run experiments and control the process.

Builds a shared QbD language across formulation, process, analytical and quality teams
Improves right-first-time development and reduces manufacturing deviations
Strengthens EMA and INFARMED submission readiness with QbD evidence
Supports robust processes for CDMO work delivered to international clients
Enables tailored training aligned to your live product pipeline
Standardises risk assessment and control-strategy practice across sites
Develops in-house capability in DoE and design-space thinking

Your QbD Career Path in PortugalHigh-Demand Pharma and Biotech Roles

Quality by Design capability is increasingly valued across Portugal's pharmaceutical, biopharmaceutical and CDMO organisations, where employers such as Bial, Hovione and Bluepharma develop products to FDA and EMA expectations. As health-sector exports grow and the country pursues European biotech leadership, professionals who invest in Quality by Design training and can design quality in are sought after in formulation, process development, analytical science, QA and regulatory affairs. Here is what the local market is telling us right now.

56,000 euros

Quality Assurance Manager salary, Lisbon

average per year, Glassdoor 2026

55,263 euros

Regulatory Affairs Manager salary, Portugal

average gross, PayScale 2026

5.6bn euros

Health-sector exports, Portugal

2025, portugalglobal.pt

1,200-1,500

Qualified jobs, Coimbra life-science park

planned, labiotech.eu 2026

SECTORS HIRING

—Pharmaceutical Manufacturing and Development
—Biopharmaceutical and Biotechnology
—Contract Development and Manufacturing (CDMOs)
—Generic and Active Pharmaceutical Ingredient Producers
—Regulatory Affairs and CMC Consulting
—Medical Devices and Advanced Therapies

GROWTH TRENDS

—Health-sector exports passed 5.6 billion euros for the first time in 2025
—Portugal is targeting European biotech leadership by 2030
—CDMO hub growth led by Hovione, Recipharm and Lusomedicamenta
—New life-science parks emerging in Coimbra and Cantanhede
—INFARMED clinical-trial assessment times falling sharply
—Rising EMA expectation for QbD evidence in submissions

Sources: Glassdoor, PayScale, SalaryExpert, ERI (Portugal) 2026; portugalglobal.pt, trade.gov and labiotech.eu (Portugal life-sciences data) 2025-2026.

Designation

Quality by Design Professionals in Portugal : Salary Insights and Trends

Hiring Companies in Portugal

€28K

Min

€38K

Average

€52K

Max

SalaryExpert · PayScale · Glassdoor (Portugal) 2026

BluepharmaHovioneTecnimedeMedinfar

Source: Bluepharma · Hovione · Tecnimede · Medinfar

Pressures Reshaping Pharmaceutical Development in Portugal

Rising Regulatory Expectations

The EMA and INFARMED increasingly expect QbD evidence in pharmaceutical submissions, so development teams need working fluency in QTPP, CQAs, design space and control strategy.

QbD builds QTPP, CQA and design-space capability

CDMO Growth Demands Robust Processes

Portugal's expanding CDMO base, including Hovione, Recipharm and Lusomedicamenta, must deliver right-first-time processes for global clients, which depends on QbD process understanding.

QbD builds right-first-time process understanding

Export-Led Quality Standards

With health-sector exports above 5.6 billion euros, Portuguese products must meet FDA and EMA quality expectations that are built in by design rather than tested in at the end.

QbD embeds FDA and EMA quality expectations

A QbD Tools Skills Gap

Portugal has deep scientific talent but limited hands-on experience in Design of Experiments, formal risk assessment and control-strategy design, the exact skills QbD develops.

QbD gives hands-on DoE and risk-assessment skills

Biologics and Complex Molecules

A growing biotech pipeline in monoclonal antibodies and advanced therapies needs QbD to identify critical quality attributes and control process-defined products reliably.

QbD extends to biologics and advanced therapies

Capital and Right-First-Time Pressure

Margin and capital discipline push organisations to build quality in rather than test it in, cutting rework and deviations through better process understanding.

QbD builds portfolio and process optimisation skills

Sources: trade.gov, portugalglobal.pt, labiotech.eu and European Biotechnology (Portugal pharma and CDMO) 2025-2026; ICH Q8 to Q11 guidelines.

QbD is more than a method. It is the way modern pharma builds quality into products. Join professionals in Portugal who design quality in from the start and deliver consistent, submission-ready development. Start your journey today.

Your Portugal Career Transformation

From Trial-And-Error to Design-Led Development

What QbD Training Changes for You

Portugal's pharmaceutical and CDMO sector is expanding on the back of rising exports and a national push toward biotech leadership, and employers increasingly value professionals who can design quality in. Here is which side of that line you want to be on.

Today

Seen as a capable scientist without a systematic quality method

After QbD

Recognised for QbD capability that Portugal's pharma, biotech and CDMO employers actively seek

Today

Seen as a capable scientist without a systematic quality method

Today

Progression tied to lab and delivery roles with limited leverage

After QbD

Positioned for QA and regulatory roles where Portuguese salaries reach well beyond entry bands

Today

Progression tied to lab and delivery roles with limited leverage

Today

Contributing to submissions without owning the quality narrative

After QbD

Able to build QTPP, CQA and control-strategy evidence for EMA and INFARMED submissions

Today

Contributing to submissions without owning the quality narrative

You master QbD

Before

Development driven by trial and error and end-product testing

Now you have

A structured, science-based QbD method that designs quality in from the start

Before

Development driven by trial and error and end-product testing

Before

Limited exposure to what ICH guidelines expect of pharmaceutical development

Now you have

Working fluency in the ICH Q8 to Q11 framework that regulators and CDMO clients expect

Before

Limited exposure to what ICH guidelines expect of pharmaceutical development

Before

Risk decisions based on habit, prior batches and instinct

Now you have

Formal risk assessment with Ishikawa and FMEA to prioritise what truly matters

Before

Risk decisions based on habit, prior batches and instinct

Before

DoE and design space seen as specialist territory beyond your role

Now you have

The confidence to plan a DoE, read a design space and set a control strategy

Before

DoE and design space seen as specialist territory beyond your role

"The gap between testing quality at the end and designing it in from the start is exactly what today's regulators and international clients reward."

Join professionals across Portugal who trained with Invensis Learning and made the shift.

Sources: Glassdoor, PayScale, SalaryExpert, ERI (Portugal) 2026.

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 Portugal 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.

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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.

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

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

100% Secure and Safe download

Skills You Will Build in This QbD CourseTools You Can Apply on Live Projects

In this Quality by Design course you will learn to design quality into pharmaceutical products from the outset. By the end of the programme you can move from a Quality Target Product Profile through risk assessment and Design of Experiments to a defined design space and a documented control strategy, using worked small-molecule and biologic examples.

Set the Quality Target Product Profile

Learn to construct a QTPP from clinical and patient needs so that every formulation and process decision is anchored to what the product must achieve for quality, safety and efficacy.

Identify and Classify Critical Quality Attributes

Determine which physical, chemical and biological attributes are critical to quality, and link each CQA to Critical Material Attributes and Critical Process Parameters.

Run Structured Risk Assessments

Apply Ishikawa diagrams and FMEA with Severity, Occurrence and Detectability scoring to prioritise the material attributes and process parameters that drive product quality.

Design and Interpret DoE Studies

Plan screening and response-surface Design of Experiments, interpret the model output, define the design space, and set Normal Operating and Proven Acceptable Ranges.

Apply PAT and Build a Control Strategy

Use Process Analytical Technology such as NIR and Raman for real-time monitoring, then turn QbD outputs into a robust, risk-proportionate control strategy for manufacturing.

Structure QbD Evidence for Submissions

Present QTPP, CQA, risk-assessment, design-space and control-strategy evidence in the CTD Section 3.2.P.2 format that the EMA and INFARMED expect in pharmaceutical submissions.

Who Should TakeQuality by Design Training in Portugal?

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 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 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

EUR 430

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 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 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

Untitled

Please Note: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.

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

Loading schedules…

Why Choose Invensis Learning for QbD in PortugalPractical, Instructor-Led, ISO-Certified

Invensis Learning delivers structured Quality by Design training for pharmaceutical, biopharmaceutical and CDMO professionals across Portugal who want practical, ICH-aligned capability. Our programmes combine experienced trainers, hands-on exercises, organised courseware and learner-focused support. As an ISO 9001:2015 and ISO 27001:2022 organisation, we deliver a professional learning experience built around real-world application and measurable outcomes, whether you enrol as an individual or arrange corporate training for your team.

Experienced, industry-practitioner trainers with real pharmaceutical and quality expertise
Flexible formats: live virtual, classroom, onsite and customised corporate training
Practical, hands-on QbD exercises using realistic development scenarios
ICH-aligned courseware covering QTPP, CQAs, risk assessment, DoE and control strategy
Dedicated learner support before, during and after the programme
Scalable delivery for local, regional and global teams
Course completion record provided on finishing the programme
Trusted by professionals and organisations across many industries and regions

1-to-1

Doubt-Clearing Sessions

60+

Global Course Portfolio

100+

Countries Served

ISO 9001

Quality Management

ISO 9001:2015 Certified

ISO 27001:2022 Certified

Secure SSL Encryption

Leaders in Training industry for 12+ years

Over 5000 five star reviews

Level AA conformance, W3C WCAG 2.2

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

Quality by Design in Portugal

Four Seasons Ritz, R. Rodrigo da Fonseca 88, 1099-039 Lisboa, Portugal

Quality by Design in Portugal

Reid's Palace, A Belmond Hotel, Estrada Monumental 139, 9000-098 Funchal, Portugal

Quality by Design in Portugal

Four Seasons Ritz, R. Rodrigo da Fonseca 88, 1099-039 Lisboa, Portugal

Quality by Design in Portugal

Reid's Palace, A Belmond Hotel, Estrada Monumental 139, 9000-098 Funchal, Portugal

Corporate QbD Training in PortugalUpskill Your Whole Team

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Suitable for small, medium and large development and quality teams
Customised schedules aligned to your team availability
Flexible delivery through onsite, live virtual or hybrid formats
Trainers with real pharmaceutical and quality-management expertise
Role-based examples mapped to your live product pipeline
Dedicated coordination and learner support for group programmes
Scalable delivery for teams across Portugal and global sites

What Our Learners Say

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A Method I Can Actually Apply

"The QbD training finally connected the tools I half-knew into one method. I can now build a QTPP, run an FMEA and plan a DoE with a clear reason for every step. The pharmaceutical case studies made it immediately usable at work."

Ana Sofia Marques

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Changed How I See My Lab Work

"As an analytical scientist, the sessions on CQAs and control strategy changed how I think about method development. I understand far better how my testing fits into the wider design space and the overall quality picture."

Tiago Fernandes

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Perfect for Regulatory Work

"The trainer explained how QbD evidence maps to Section 3.2.P.2 of the submission, which was exactly what I needed. I feel much more confident preparing the pharmaceutical development section for EMA and INFARMED filings."

Beatriz Costa

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A Shared Language for Our Teams

"We ran the QbD programme onsite for our development and quality teams and it gave everyone a shared language for risk assessment and design space. Our cross-functional reviews are noticeably sharper and faster now."

Rui Almeida

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Practical and Tailored to Us

"As an L&D lead in a biopharmaceutical company, I wanted practical capability, not slides. Invensis delivered a tailored, hands-on session and our scientists applied QbD tools to a live project the same week. Strong, measurable value."

Mariana Silva

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4.6

Ratings

100K+

Happy Learners

100+

Locations Worldwide

99%

Training Satisfaction

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

Quality by Design is a systematic, science-based approach to pharmaceutical development that builds quality into a product from the design stage rather than testing it in at the end. It uses tools such as the QTPP, Critical Quality Attributes, risk assessment, Design of Experiments, the design space and a control strategy, aligned to ICH Q8(R2), Q9, Q10 and Q11.

General

What is Quality by Design (QbD)?

Who should attend this QbD training in Portugal?

The programme suits formulation scientists, process development engineers, analytical scientists, QA professionals, regulatory affairs and CMC specialists, and manufacturing managers in pharmaceutical, biopharmaceutical, API, CDMO and medical device organisations across Portugal who want to apply QbD in development and submissions.

Is QbD relevant to Portugal's pharmaceutical and CDMO sector?

Yes. Portugal's pharmaceutical, biotech and CDMO base, including companies such as Bial, Hovione and Bluepharma, develops products to FDA and EMA expectations, and the EMA and INFARMED increasingly expect QbD evidence in submissions, making these skills highly relevant locally.

Do I need prior QbD experience to join?

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

Which ICH guidelines does the course cover?

The training covers the ICH quality framework behind QbD: Q8(R2) Pharmaceutical Development, Q9 Quality Risk Management, Q10 Pharmaceutical Quality System and Q11 for drug substances, along with related FDA and EMA expectations and PAT guidance.

Pricing

How much does the QbD training cost in Portugal?

Pricing varies by delivery format, group size and schedule, so exact fees are available on request. Share your preferred format and team size and a learning advisor will provide a tailored quote for Portugal.

What is included in the course fee?

The fee typically includes instructor-led delivery across all QbD modules, ICH-aligned courseware, hands-on tool exercises, worked pharmaceutical and biologic case studies, learner support, and a course completion record from Invensis Learning.

Do you offer group or corporate pricing?

Yes. We offer corporate group training with customised schedules and volume-based pricing for R&D, quality and regulatory teams. It is ideal for training a cross-functional team on a live product project. Ask about corporate pricing for your team.

What payment options are available?

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

Is this training available online in Portugal?

Yes. The programme is available as online, live virtual instructor-led training as well as classroom and onsite formats, so teams across Portugal can join without travel. Request a quote to see upcoming schedules.

Assessment

Is there an exam for the QbD training?

No. This is a practical, non-assessed skills programme with no examination. Learning is reinforced through hands-on QbD tool exercises, pharmaceutical case studies and group discussion across the one-day programme.

What will I receive on completing the training?

You receive a course completion record from Invensis Learning. The training builds practical QbD skills that are immediately applicable to pharmaceutical product and process development projects.

How is learning reinforced without a test?

Learning is reinforced through applied practice. You build a QTPP, identify CQAs, run an Ishikawa and FMEA risk assessment, and interpret a design space using realistic development scenarios, so you leave able to use the tools at work.

How long is the QbD training?

The programme is delivered in one day, covering QbD principles and the ICH framework, QTPP and CQAs, risk assessment, DoE and design space, PAT and control strategy, and QbD in practice, with hands-on exercises throughout.

Are there any prerequisites or entry requirements?

None. The course is open to all and introduces QbD from first principles. A science or engineering background in pharmaceutical development or manufacturing helps you get the most from it, but it is not required.

Course Content

What topics does the QbD syllabus cover?

The syllabus spans QbD principles and the ICH regulatory context, the Quality Target Product Profile and Critical Quality Attributes, risk assessment with Ishikawa and FMEA, Design of Experiments and the design space, Process Analytical Technology and control strategy, and QbD in practice through case studies.

What will I learn about DoE and the design space?

You will learn why Design of Experiments replaces one-factor-at-a-time testing, how to select screening and response-surface designs, how to interpret the model, and how to define the design space with Normal Operating and Proven Acceptable Ranges.

Does the course cover both small molecules and biologics?

Yes. The training includes worked examples for small-molecule drug products such as tablets and injectables, and for biologics such as monoclonal antibodies, covering CQAs like potency, glycosylation, charge variants and aggregation.

What hands-on exercises are included?

You will construct a QTPP, identify and classify CQAs, build an Ishikawa diagram, complete an FMEA-based risk assessment, select a DoE design and interpret a design space, all applied to realistic pharmaceutical development scenarios.

What is a QTPP and is it covered in the course?

The Quality Target Product Profile is a prospective summary of the quality characteristics a product should achieve for quality, safety and efficacy. Yes, building the QTPP is covered in depth and is the starting point of every QbD programme.

Enrollment

How do I enrol in the QbD course in Portugal?

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. See upcoming batches or talk to a learning advisor to get started.

What training formats are available?

We offer online, live virtual instructor-led training, classroom sessions, onsite delivery and customised corporate group training, so you can choose the format that best fits your schedule and team.

Can the course be delivered onsite for our team in Portugal?

Yes. We deliver onsite and live virtual corporate training for teams across Portugal, tailored to your product pipeline so participants can apply QbD tools to their own live development projects. Ask about corporate delivery for your team.

When can I start?

New sessions run regularly in live virtual and classroom formats, and onsite corporate sessions are scheduled to suit your team. Request a quote to see the next available dates for Portugal.

What is the reschedule or refund policy?

Rescheduling and refunds are handled per our published policy, and selected plans include flexible reschedule options. Reach out to our team for the details that apply to your enrolment.