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GxP Training Excellence
Trusted by Leading Life Science Companies

Mastering GxP: Advanced Training
for
Life Sciences

Empowering excellence and compliance with expert-led programs
built to meet global GMP, GDP, GCP, and GLP requirements.

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Regulatory Training
FDA & EMA Recognized Certifications

Expert GxP Training
for Life Sciences Professionals

21 CFR Part 11 compliant certificates recognized by FDA, EMA,
and global regulatory bodies. Train your team today.

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CEU/CPD Accredited Programs

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in Life Sciences

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CEU/CPD accredited programs for GMP, GLP, GCP, and more.

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GxP Services

Explore Our Trainings & Operations

We provide training programs designed to help you meet quality and compliance standards. Our courses cover GMP, GLP, GCP, Cleanroom Practices, GDP, and Quality Assurance.

GMP

Good Manufacturing Practices

Ensuring products are consistently produced and controlled according to quality standards for their intended use. Our training builds expertise in process validation, contamination control, documentation, and facility compliance across all manufacturing environments—from APIs to finished dosage forms.

GLP

Good Laboratory Practices

Promoting the reliability and integrity of non-clinical safety data. Our programs focus on study planning, execution, documentation, and quality systems in analytical and toxicology labs—ensuring data is traceable, reproducible, and acceptable to global regulators.

GCP

Good Clinical Practices

Protecting the rights, safety, and well-being of clinical trial participants while ensuring data credibility. We train sponsors, monitors, and investigators on protocol adherence, informed consent, ethics oversight, and trial documentation in accordance with ICH E6 and regional regulations.

GDP

Good Distribution Practices

Maintaining product quality and integrity throughout the entire supply chain. We train teams in proper storage, transportation, cold chain management, serialization, and documentation practices to prevent falsified medicines from entering the supply chain and ensure patient safety.

CS

Cleanroom Standards

Controlling contamination in critical manufacturing environments. Our training covers ISO classifications, aseptic techniques, environmental monitoring, gowning procedures, and facility design—essential for sterile product manufacturing in pharmaceuticals, biologics, and medical devices.

QA

Quality Assurance (QA)

Building a proactive, system-wide culture of prevention. We develop QA professionals in quality systems, risk management, deviation handling, change control, audit readiness, and continuous improvement—ensuring sustainable compliance beyond just checking boxes.

Training programs are designed in accordance with global regulations and the guidelines of key regulatory bodies, including the FDA, EMA, and PMDA, and are structured around critical international standards such as the ICH guidelines (Q, S, E, M series), WHO norms, and ISO requirements.

Regulatory

Regulatory Authorities

Government bodies with enforcement power

  • FDA – USA
  • EMA – EU
  • PMDA – Japan
  • Health Canada
  • TGA – Australia
  • CDSCO – India
  • NMPA – China
Harmonization

International Bodies

Develop consensus guidelines globally

  • ICH – International Council for Harmonisation
  • WHO – World Health Organization
Standards

Standards Organizations

Create technical and quality standards

  • ISO – Quality Management Standards
  • PIC/S – GMP Inspection Practices
  • USP / EP / JP – Pharmacopoeias
Networks

Regional Networks

Facilitate regulatory cooperation

  • ASEAN – Southeast Asia Network
  • GCC – Gulf Cooperation Council
  • AMRH – African Harmonization
  • FDA/EMA – Bilateral Agreements
Ethics

Ethics & Clinical Trial Oversight

Ensure ethical research conduct

  • IRBs / ECs – Review Boards
  • CIOMS – Medical Sciences Council
  • Helsinki Declaration – Ethics Guidelines
Industry

Trade Associations

Influence policy and standards

  • PhRMA – USA Manufacturers
  • EFPIA – European Federation
  • DIA – Drug Information Association

Our GxP training programs are tailored to meet the regulatory, quality, and operational needs of each major life sciences sector. The following outlines key industry categories and their training requirements.

Pharmaceuticals

Small Molecules

Traditional chemically synthesized compounds

  • Examples: Tablets, capsules, injectables
  • Regulators: FDA, EMA, PMDA
  • Focus: Process validation, impurity profiling, data integrity
Biologics

Biopharmaceuticals

Complex products from living systems

  • Examples: Antibodies, vaccines, blood products
  • Regulators: FDA (CBER), EMA
  • Focus: Aseptic processing, viral clearance, cold chain
Advanced

ATMPs

Gene & cell therapies, personalized medicine

  • Examples: CAR-T, gene vectors, stem cells
  • Regulators: FDA (CBER), EMA (CAT)
  • Focus: Chain of identity, donor traceability
Devices

Medical Devices & IVDs

Instruments and diagnostic equipment

  • Examples: Implants, diagnostics, surgical tools
  • Regulators: FDA (CDRH), EMA/NB
  • Focus: Design controls, biocompatibility, UDI
Controlled

Cannabis & Controlled Substances

Cannabis products and regulated drugs

  • Examples: Medical cannabis, cannabinoid APIs
  • Regulators: FDA, DEA, Health Canada
  • Focus: Seed-to-sale tracking, secure storage
Combination

Combination Products

Drug/device or biologic/device products

  • Examples: Drug-eluting stents, prefilled syringes
  • Regulators: FDA (OCP), EMA
  • Focus: Mode of action, interface testing

We provide integrated, current training aligned with major regulatory frameworks to support your global operations.

Excellence

Our Commitment to Quality

GxP Trainings is committed to being a trusted global leader in GxP and regulatory training impartation. We achieve this by designing, developing, and delivering training solutions that consistently meet and exceed the expectations of our clients, learners, and regulatory stakeholders.

Accuracy

Our Core Quality Principles

To fulfill this commitment, we adhere to the following principles:

  • Learner-Centric Excellence
  • Regulatory & Technical Accuracy
  • Continuous Improvement
  • Expertise & Integrity
  • Reliable & Compliant Service
Innovation

Quality Objectives

We will measure our success against the following key objectives, which are regularly monitored and reviewed by Top Management:

  • Maintain a client satisfaction score of ≥ 95%.
  • Achieve a learner competency assessment pass rate of ≥ 90%.
Innovation

Quality Objectives

  • Ensure 100% of course content is reviewed and updated bi-annually or in response to critical regulatory changes.
  • Deliver 99% of scheduled training programs without cancellation.
  • Resolve any client feedback or non-conformity within 5 business days.
Integrity

Leadership Commitment

Top Management at GxP Trainings pledges to lead this quality initiative by providing the necessary resources, fostering a culture of quality, and ensuring this policy is communicated, understood, implemented, and maintained at all levels of the organization.

Our Popular Courses

Our life sciences GMP training programs deliver regulator-aligned, practical learning for professionals operating in highly regulated environments. We offer comprehensive training in GMP, GDP, GLP, GCP, Pharmacovigilance, Medical Device Regulations, Pharmaceutical Quality Assurance, and Cleanroom Operations. All programs are led by industry experts and focused on real-world application, inspection readiness, and compliance with global regulatory standards, including FDA, EU-GMP, Health Canada, and WHO.

GMP API
Popular
Good Manufacturing Practices – API & Intermediates (ICH Focused)

41 Lessons
All Levels
EU GMP Training
Trending
Good Manufacturing Practices (EMA Focused)

41 Lessons
All Levels
Featured
Good Clinical Practices (ICH Focused)

10 Lessons
All Levels
OECD GLP
Popular
Good Laboratory Practices (OECD Focused)

13 Lessons
All Levels
Good Distribution Practices
Trending
Good Distribution Practices (GDP)

10 Lessons
All Levels
Training Facility
Flexible Learning

Training Formats

Structured learning paths for professionals seeking to advance their careers in QA, RA, GCP, PV, GMP and GLP and more.

Live Virtual Training

Instructor-led, interactive sessions with real-world case studies.

On-Demand eLearning

Self-paced courses accessible anytime, from anywhere.

Onsite Corporate Workshops

Customized training delivered directly to your team.

On-Site Shopfloor Trainings

Designed to deliver practical, role-specific learning directly at your facility.

Why Choose Us

At GxP Trainings, we are dedicated to quality, practical application, and continuous improvement in life science regulatory education.

Expert-Led Instruction

Learn from seasoned professionals with extensive real-world GxP experience, bringing unparalleled insights and practical knowledge.

Practical, Applied Learning

Our programs emphasize interactive workshops, case studies, and simulations for actionable skills directly applicable to your role.

Flexible Learning Options

Choose from online, in-person, or hybrid courses designed to fit your busy schedule and preferred learning style.

Industry-Recognized Certification

Validate your expertise with certifications highly valued by employers across the life science sector.

Continuous Support & Resources

Benefit from post-training support, access to resources, and a network of GxP professionals for sustained learning.

Current Regulatory Insights

Stay ahead with training content meticulously updated to reflect the latest global GxP regulations and industry best practices.

Start Your Journey

Join Us & Transform Your Future

Take the first step toward excellence. Our world-class programs are designed to equip you with the skills and knowledge to thrive in today's competitive landscape.

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