No deviation Delivers Specialized Training
Your operations evolve. So should your people. Empower your team with industry-ready skills and confidence.
No Deviation offers specialized training for regulated environments, with a focus on operational excellence, data integrity, and digital transformation — tailored for the pharmaceutical and biotech sectors.
Upskill with No deviation – Expert Training for a Compliant Future.
No deviation's 2025 Training Portfolio
Foundations of Compliance & Quality
Build a Strong Quality Culture from Day One
In regulated environments, quality is the foundation. Our training programs equip your teams with the mindset and skills to uphold compliance, mitigate risks, and adapt to evolving regulatory expectations.
- GMP (Good Manufacturing Practices)
This course provides an overview of the regulations pertaining to GMPs. The topics that will be covered includes manufacturing controls, product distribution, plant hygiene, documentation practices, organizational structure and more! - QRM – ICH Q9
This course covers the fundamentals for assessing and mitigating risks during product lifecycles and incorporates requirements from ICH Q9. This course sets the foundation for a safety and quality-centric approach. - Pharmaceutical Quality System (PQS)
This course introduces PQS, which is a framework that ensures product quality meets established standards throughout the lifecycle of pharmaceutical products. This course includes continual improvement and lifecycle approach, Quality Management Maturity (QMM), Process Design, QbD Principles and more! - Quality Audit for Pharmaceutical and Medical Devices
This course helps you to understand the concepts behind compliance auditing. Address the challenges of GMP auditing for the pharmaceutical industry, understand the basic competencies required to effectively perform auditor’s assigned responsibilities. Learn all about auditing! - Pharmaceutical Regulatory Landscape
This course provides participants with an understanding of the global pharmaceutical regulatory landscape, including key regulatory authorities, compliance requirements. This training ensures you stay compliant with the continually evolving pharmaceutical regulations and guidance from regulatory authorities. - Data Integrity & Data Life Cycle – This course will cover data integrity, electronic records and signatures, and the compliant operation of GxP Computerized Systems. It provides practical tools and techniques to implement effective controls that ensure the integrity and validity of the data throughout its data lifecycle.
- Deviation & CAPA Management
This course provides guidance on how to perform effective deviation investigation for true root cause, demonstrates how a mature Pharmaceutical Quality System (PQS) leverages CAPA and Continuous Improvement and explores the role of Process Performance & Product Quality Monitoring (PPPQMS) in enhancing your PQS.
Ideal for Quality professionals, QA/QC managers, regulatory affairs, and site leadership.
Let’s build your quality backbone
Engineering & Manufacturing Excellence
Bridge the Gap Between Design and Performance
From clean utility design to system qualification, our programs help engineering teams and manufacturing leaders deliver compliant, efficient facilities ready for production and inspection.
- Commissioning & Qualification (C&Q)
Gain knowledge on the science and risk-based approach to integrated lifecycle Commissioning & Qualification by conducting verification of systems, equipment and facilities in accordance with ISPE Guidelines, ICH documents Q8, Q9, and Q10, current Regulatory Guidance, industry best practices, and ASTM E2500. - System Risk Assessment
This course equips participants with the knowledge to perform effective system risk assessments, focusing on identifying, evaluating, and mitigating risks to ensure compliance, data integrity and system reliability throughout the system lifecycle. - GMP Sterile Pharmaceutical Manufacturing Facility
Learn about regulatory philosophy, aseptic process and equipment considerations, aseptic clean room design and operation, differential pressure requirements, airlocks, air filtration, HVAC design considerations, and a brief introduction to barrier isolation technology process. - Clean Utilities
This course will cover the principles of design an operation of clean utilities used in pharmaceutical manufacturing, including the essential concepts and principles of systems used to generate the clean utilities. These concepts include specification, design, operation, testing and maintenance of equipment and systems for Purified Water (PW), Water for Injection (WFI< Clean Steam, Compressed Air, Nitrogen and HVAC Systems. - Process Validation
This course help you integrate and link the science and risk-based lifecycle approach for Process Validation to your overall Pharmaceutical Quality System. It will provide you with practical application of quality risk management tools in preparation and planning for validation of your manufacturing control strategy. It will deliver statistical approaches and tools which can be used to strengthen and justify your decision-making rationale for defendable process design and process performance. - Cleaning Validation
This course covers the risk-based approach to cleaning development and verification; risk analysis; procedures and evaluation tools including FMEA / FMECA, master planning, risk control, PAT, periodic assessment and monitoring, risk review and communication.
For engineers, project managers, CQV professionals, and tech transfer teams.
Engineer with compliance in mind.
Advanced Therapies
Adapt to the New Frontier: Cell & Gene Therapies
Advanced therapies demand advanced compliance strategies. This course provides the regulatory and operational tools needed to navigate ATMP-specific challenges with confidence.
- ATMP (Advanced Therapy Medicinal Products)
Understand the science behind ATMPs, regulatory aspects and supply chain considerations of ATMPs with focus on Cell Therapies, manufacturing and facility considerations, and even technology transfer and scale-up considerations!
Targeted at ATMP manufacturers, biotech leaders, QA, and CMC teams.
Stay ahead of the curve in ATMP.
Digital Transformation Enablement
From Paper to Platform – Training for the Digital Age
Digital validation tools can transform compliance — but only if your teams are prepared. Our Kneat Gx training programs ensure users are ready to configure, execute, and optimize paperless validation with confidence.
- End User
Learn how to use Kneat Gx for general navigation, document development, review and approval, test execution, folder creation, and entity management. - Power User Level 1
Certify your competency in document templates, document packs, library properties, section group templates, and approval workflows - Power User Level 2
- End User
Designed for validation specialists, QA professionals, and potential/current Kneat users.
Digitize smarter and faster
Our Accredited Trainers
Behind every impactful training is a team of experts who’ve lived the reality of GMP environments and know how to teach it.
Our accredited trainers combine technical mastery, on-the-ground experience, and a passion for knowledge-sharing. Whether you’re rolling out a new digital system or strengthening your CQV foundations, they bring clarity, structure, and energy to every session.
Meet our core training team:
Pierre Winnepenninckx — CEO & ISPE Certified Instructor
Pierre brings over 20 years of hands-on experience in the design, qualification, and validation of GMP and vaccine facilities across Europe and Asia. A recognised figure in the global CQV community, he actively shapes best practices through his involvement with ISPE’s Commissioning & Qualification and Digital Communities of Practice.
As an ISPE-certified instructor, Pierre delivers trainings on Risk-Based CQV and Sterile Facility Pharmaceutical Quality Systems. His sessions are valued for their clarity, rigour, and forward-thinking approach.
Shanshan Liu — Technical Director & ISPE Certified Instructor
Shanshan brings over 15 years of global experience in process engineering, CQV, automation, and GMP compliance. Her dual perspective, as both consultant and end user, makes her an impactful trainer on real-world project challenges.
She serves as an ISPE International Board Member (2025–2026) and is a certified instructor in key regulatory domains, including GMP, Pharmaceutical Quality Systems, ATMPs, Audits, and more. As an IRCA-certified auditor and trainer on deviation and CAPA, she adds strong regulatory insight to every course.
Her sessions connect technical execution, data integrity, and regulatory expectations especially valuable in GMP remediation contexts.
JoonLeong Ng — Business Director & Kneat Certified Trainer
Joon has built his career across the APAC region, specialising in CQV for pharma and biotech. With 15 years of hands-on and leadership experience, he’s fluent in both technical execution and project governance.
A Kneat Academy certified trainer for End user, Power User Level 1 and Power User Level 2 Trainings, Joon trains teams on digital validation with clarity, rigour, and process excellence. He also brings deep expertise in regulatory frameworks, change control, and lean leadership, key skills he transfers in every session.
Shanta Latchumy Geevaretnam — Technical Lead, Kneat Certified Trainer
Accredited by the Kneat Academy, Shanta is a go-to expert for digital validation in highly regulated environments. Her trainings empower teams to work confidently and compliantly with Kneat Gx whether they’re starting out or scaling up.
As a Kneat Certified Trainer and Super User, she combines platform mastery with hands-on implementation tips to drive adoption, accuracy, and audit-readiness.
🔹 All our trainers are active consultants — not just theorists — bringing real-time industry challenges into the classroom.
🔹 Trainings can be adapted to your site, your goals, and your team’s maturity level.
Why Train with No deviation?
At No deviation, we combine deep industry experience with a hands-on, practical approach to learning. Our trainers are not only educators, they’re also seasoned professionals who bring real-world insights from pharmaceutical projects across the globe.
We deliver content that’s aligned with EMA, FDA, and PIC/S expectations, ensuring your teams are always audit-ready. Whether you prefer virtual sessions, on-site workshops, or a blended format, our flexible delivery adapts to your operations.
Each course is built around practical examples and case studies, so your team can apply what they learn immediately and effectively.
Get Started Today
Whether you’re scaling operations, going digital, or onboarding new talent — we have a course to match your goals.
👉 Let’s co-design your 2025 training plan.
