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Corporate & Team Training

Train Your Entire Team. Meet Your Compliance Obligations.

Regulatory compliance is a team responsibility — not an individual one. Whether you are preparing for an FDA inspection, onboarding a new quality team, or meeting your annual GMP training obligations, GxP Trainings provides structured, regulatory-aligned online training your entire organisation can complete on their schedule.

50+
Expert Courses
10k+
Professionals Trained
21 CFR
Part 11 Compliant Certs
5+
Min. Group Size for Discount

Why Companies Choose GxP Trainings for Team Training

Our corporate training packages are designed for pharmaceutical manufacturers, biotech companies, CROs, medical device firms, and supply chain organisations that need documented, verifiable training across multiple team members.

Regulatory-Aligned Content

All courses are aligned with FDA 21 CFR Parts 210 & 211, EMA EudraLex Volume 4, ICH Q7, ICH E6(R3), and WHO GMP guidelines — the same frameworks your team will be audited against.

21 CFR Part 11 Compliant Certificates

Every team member who completes a course receives a digital certificate compliant with 21 CFR Part 11. These can be used as documented training records during FDA inspections, EMA audits, and internal compliance reviews.

Self-Paced — Zero Scheduling Conflicts

Your team completes training at their own pace, on any device, without disrupting production schedules or shift patterns. No classroom, no travel, no fixed dates.

Individual Progress Tracking

Each team member has their own account. Managers can monitor who has completed which course and download certificates for training records.

Scalable for Any Team Size

From a QA team of 5 to a manufacturing organisation of 500+ — our group enrollment options scale to your needs with volume discounts for teams of 5 or more.

12-Month Access Per Enrolment

Each team member has 12 months from enrollment date to complete their course. Most courses are completed in 5–10 hours of self-paced study.

Who Is Corporate Training For?

Our corporate training packages are ideal for regulated organisations across the pharmaceutical, biotech, clinical research, medical device, and distribution sectors. Whether you are preparing for an upcoming inspection or fulfilling annual training obligations, we have a program for your team.

Pharmaceutical Manufacturers
  • GMP training for production, QA, QC, and engineering teams
  • Annual GMP refresher training for all manufacturing personnel
  • Pre-inspection training to ensure all staff are current on FDA and EMA requirements
Biotech & Biopharmaceutical Companies
  • GMP training aligned with FDA and EMA biologics requirements
  • ICH Q7 training for API manufacturing teams
Contract Research Organisations (CROs)
  • GCP training for clinical research associates, monitors, and site staff
  • ICH E6(R3) training aligned with the 2025 update
Medical Device Manufacturers
  • GMP training for quality and manufacturing teams
Pharmaceutical Distributors & 3PLs
  • GDP training for warehouse, logistics, and supply chain teams
  • Cold chain management and temperature monitoring training
Regulatory Affairs & Quality Teams
  • Cross-functional GxP training across GMP, GCP, and GDP disciplines

How Corporate Enrollment Works

Getting your team enrolled is straightforward. We handle the setup so your team can focus on completing their training. Group quotes are provided within 24 hours.

1

Contact Us

Tell us how many team members need training, which courses are required, and your target completion timeline. We will provide a group quote within 24 hours.

2

Receive Enrollment Link

We set up your organisation in our system and provide a dedicated enrollment link for your team.

3

Team Completes Training

Each team member creates their own account, enrolls in the relevant course, and completes the modules at their own pace.

4

Download Certificates

On completion, each team member downloads their 21 CFR Part 11 compliant certificate — ready to use as training records in your QMS.

What Your Team Will Learn

All training content is developed by subject matter experts, mapped directly to regulatory requirements, and updated to reflect current guidance and inspection trends.

GMP Training ICH Q7 / FDA / EU GMP

  • Regulatory background: FDA 21 CFR Parts 210 & 211, EudraLex Volume 4, ICH Q7
  • Core GMP principles: documentation, SOPs, personnel, facilities, equipment
  • Data integrity and 21 CFR Part 11 / EU GMP Annex 11
  • GMP for APIs: ICH Q7 requirements
  • Common GMP deficiencies and FDA 483 observations
  • Validation: IQ, OQ, PQ, process validation
  • Change control, deviation management, CAPA

GCP Training ICH E6(R3)

  • ICH E6(R3) Good Clinical Practice principles — 2025 update
  • Sponsor responsibilities and oversight
  • Investigator responsibilities and site management
  • Informed consent procedures
  • Trial Master File (TMF) management
  • Risk-based monitoring and decentralised clinical trials
  • Data integrity in electronic clinical systems

GDP Training WHO / EU GDP

  • WHO and EU GDP guidelines for pharmaceutical distribution
  • Cold chain management and temperature excursion handling
  • Storage conditions and warehouse requirements
  • Transportation and logistics compliance
  • Supplier qualification and auditing
  • Documentation and traceability requirements

Training Records Ready for Regulatory Inspection

Every corporate training package includes full compliance documentation for each team member. These records satisfy training documentation requirements under major global regulatory frameworks.

  • FDA 21 CFR Part 211.68 / 820.25
  • EU GMP EudraLex Volume 4, Chapter 2
  • ICH E6(R3) GCP
  • WHO GMP training requirements
Individual Completion Certificates
21 CFR Part 11 compliant digital certificates for each team member, downloadable as PDF.
Course Completion Records
Full records showing course name, completion date, assessment score, and certificate ID.
Verifiable Certificates
Each certificate has a unique ID verifiable at gxptrainings.com/verify-certificate/ — accepted during FDA inspections and EMA audits.
LMS / QMS Compatible
Certificates provided as downloadable PDFs — upload directly to any LMS or quality management system.

Frequently Asked Questions

Q How many people can enroll in a corporate package?

There is no minimum or maximum. We accommodate teams of 5 to 500+. Contact us for group pricing based on your team size.

Q Can different team members take different courses?

Yes. You can mix and match courses — for example, your QA team takes GMP training while your clinical team takes GCP training.

Q How long does each team member have to complete the course?

12 months from enrollment date. Most courses can be completed in 5–10 hours of self-paced study.

Q Can we get a discount for large teams?

Yes. Group discounts are available for teams of 5 or more. The larger the group, the greater the discount. Contact us for a custom quote.

Q Are the certificates accepted during FDA inspections?

Yes. Our certificates are 21 CFR Part 11 compliant and accepted as valid training records during FDA inspections and EMA audits.

Q Can we use these certificates in our LMS / quality management system?

Yes. Certificates are provided as downloadable PDFs and can be uploaded to any LMS or QMS.

Q Do you offer customised training content?

Our current courses are standardised and regulatory-aligned. For fully customised content, contact us to discuss your requirements.

Q How quickly will we receive a group quote?

We respond within 24 hours with a group quote and enrollment details. Simply contact us with your team size, courses required, and target completion date.

Ready to Train Your Team?

Contact us with your team size, courses required (GMP, GCP, GDP, EU GMP — or a combination), and target completion date. We respond within 24 hours with a group quote and enrollment details. Or email us directly: info@gxptrainings.com

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