For Businesses & Organisations

Elevate Your Workforce with Expert GxP Compliance Training

Customised regulatory compliance training designed for pharma and biotech organisations. Aligned with USFDA, MHRA, EMA, and WHO-GMP standards — delivered virtually by industry experts.

GxP Compliant ISO 9001:2015 Certified Virtual Delivery Structured Reporting

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Workforce Development

Elevate Your Team's Compliance Capability

Zypliance partners with pharmaceutical and biotech organisations to deliver targeted, role-relevant GxP training programmes — building a culture of compliance from the ground up.

Tailored to Your Organisation
Training customised to your SOPs, processes and regulatory environment
ISO 9001:2015 Backed Quality
All programmes developed under our certified Quality Management System
Measurable Outcomes
Structured pre/post assessments with documented compliance improvement reporting
100% Virtual Delivery
Flexible online sessions — no travel costs, scheduled around your operations

Our Training Solutions

Industry Compliance Training Solutions

Comprehensive GxP programmes built for regulated pharma and biotech environments.

About Zypliance Industry Training

Zypliance is a specialist pharma compliance education provider offering bespoke training programmes for organisations operating in regulated pharmaceutical and biotechnology environments. Our training is built for real-world application — covering GxP principles, quality systems, data integrity and regulatory expectations across international markets.

USFDA Aligned MHRA Aligned EMA Aligned WHO-GMP Aligned ISO 9001:2015

Our Approach

We begin with a training needs analysis to understand your team's compliance maturity, then design a structured programme with defined learning objectives, interactive delivery, and measurable competency outcomes aligned to your regulatory obligations.

Pricing Model

Our training is offered on a per-person / per-head basis, allowing organisations to scale training efficiently according to team size. Contact us for a tailored quote based on your programme requirements and number of participants.

Delivery Format

All training is delivered 100% virtually through live interactive sessions facilitated by subject matter experts with hands-on pharma industry experience — ensuring relevant, practical learning across your entire team regardless of location.

Reporting & Documentation

On completion, your organisation receives a structured training completion report with individual assessment scores and competency records — supporting your audit readiness and training documentation requirements.

Why It Works

The Benefits of Zypliance Training

Tangible compliance improvements that protect your operations and people.

Reduced Onboarding Time

Bring new hires up to GxP compliance standards faster with structured, role-relevant programmes that accelerate competency.

Documentation Discipline

Build strong data integrity habits and ALCOA+ documentation practices across your team — reducing errors and deviation incidents.

Audit Confidence

Teams trained to international regulatory standards are better prepared to face USFDA, MHRA, EMA and WHO inspections with confidence.

Measurable Improvement

Pre and post-training assessments demonstrate competency gains and provide documented evidence of compliance improvement.

Structured Reporting

Completion certificates and training records for every participant — audit-ready documentation at your fingertips.

Flexible & Scalable

From a team of 10 to 500+, our virtual delivery model scales seamlessly to your operational needs.

Delivery Model

What We Cover

Regulatory standards and training topics available across all programmes.

Regulatory Standards Covered

Our programmes are aligned with the world's leading pharmaceutical regulatory authorities:

USFDA — 21 CFR Part 11, 210, 211
MHRA — UK Good Manufacturing Practice
EMA — EU GMP Annex 1 & 11
WHO Good Manufacturing Practice
ICH Q10 Pharmaceutical Quality System

Training Topics Available

GMP Fundamentals Data Integrity & ALCOA+ QMS Implementation Computer System Validation Deviation & CAPA Management Change Control Aseptic Technique Contamination Control Audit Preparation Risk Management SOP Writing & Review GxP Documentation Supplier Qualification Cleanroom Standards