GMP training programmes

Practical, up-to-date GMP training for professionals in the pharmaceutical and life-sciences industry, delivered by experienced trainers.

Our GMP training covers facility design, hygiene, documentation, quality control, risk management and more, with a team of experienced trainers and a deep understanding of regulatory requirements.

Programmes are delivered on site and tailored to your dosage forms, procedures and people, with assessment so that training effectiveness can be evidenced.

Training topics

Each topic can be delivered as a standalone session or combined into an induction or refresher programme.

Facility design and GMP requirements

Designing pharmaceutical facilities that meet GMP requirements for different dose forms and routes of administration.

Good hygiene and sanitation

Principles of hygiene and sanitation in manufacturing environments to prevent contamination.

Management responsibilities

The role of management in maintaining GMP compliance and fostering a culture of quality.

Investigations, deviations and CAPA

Conducting effective failure investigations and developing corrective and preventive action plans.

Complaints, quality defects and recalls

Managing complaints, quality defects and recalls promptly and in compliance with regulatory requirements.

Cleaning validation

Principles and practice of cleaning validation to prevent cross-contamination.

Production operator certification

Certification programmes that equip operators to maintain process control and GMP compliance.

Pest control management

Effective pest-control measures for pharmaceutical facilities.

Documentation and records

Accurate, complete documentation and record-keeping for traceability and accountability.

Supplier assurance

Managing and assuring supplier quality across the pharmaceutical supply chain.

Good quality control laboratory practice

Establishing and maintaining good practice in QC laboratories for reliable results.

Validation and qualification

Process validation and equipment qualification principles and techniques.

Pharmaceutical quality systems and ICH Q10

Key elements of the pharmaceutical quality system and the ICH Q10 guideline.

Quality risk management

Principles and tools for identifying, assessing and mitigating risk in manufacturing processes.

Self-inspections

Conducting self-inspections that identify gaps and drive continuous improvement.

Change management

Managing and implementing change while maintaining GMP compliance.

Formats

Training delivered the way your site needs it

01

New-hire GMP induction

Foundation programme for new starters before they work in GMP areas.

02

Annual GMP refresher

Keeps experienced staff current with requirements and site procedures.

03

Targeted sessions

Following deviations, audits or inspections, focused on the specific gap.

04

Train-the-trainer

Equips internal quality staff to deliver and assess GMP training themselves.

How we deliver

Practical, assessed, documented

  1. Step 1

    Tailor

    Content is built around your dosage forms, procedures and equipment.

  2. Step 2

    Deliver

    Sessions run on site, led by experienced trainers using real examples from your operation.

  3. Step 3

    Assess

    Each session closes with an assessment so effectiveness can be evidenced.

  4. Step 4

    Record

    Attendance and assessment records are provided for your training files.

Training questions

Q1Are GMP training programmes necessary for employees?

Yes. GMP training is essential for employees at all levels. It ensures people understand and follow GMP requirements, perform their duties correctly and contribute to a culture of quality and compliance.

Build a training programme for your site.