Comprehensive GXP Training Programs
At EPiC we are able to use our technical knowledge, industry experience, and expertise as ex MHRA Inspectors, to help companies educate their staff to gain the required understanding of GXP, and the importance of compliance, in order to protect patient safety and facilitate the manufacture and supply of safe and efficacious high-quality products and ensuring the robustness and reliability of clinical trial data used in regulatory decision making.
Our experts use their industry experience and technical knowledge to educate and mentor your staff, including Senior Managers, on GXP requirements and the importance of compliance. We will support you in ensuring your personnel are trained and competent to generate reliable clinical trials data and manufacture and supply safe and effective products.
Regulatory GXP Compliance Training
This training focuses on the global regulatory environment, including guidelines set by bodies such as the FDA, EMA, ICH and WHO. It helps companies ensure compliance with these regulations, minimizing the risk of penalties and product recalls.
GXP Quality Management Systems (QMS) Training
This service includes training on the development and maintenance of robust QMS, covering documentation, record-keeping, and the roles and responsibilities of various personnel. It ensures that companies can uphold GXP regulations consistently.
GXP Refresher Courses
These are designed for professionals who need to stay updated with the latest GXP changes to legislation and guidance and gain an awareness of planned future changes. Refresher courses help maintain a high level of competency and awareness in the industry and are an essential part of building resilient systems to ensure compliance.
GXP Customised Training Solutions
We can also offer tailored training programs to meet the specific needs of an organisation. This can include on-site training, workshops, and seminars focused on particular aspects of GXP relevant to the company’s operations.
These services are essential for ensuring that pharmaceutical manufacturing and clinical trial processes are safe, efficient, and compliant with regulatory standards, ultimately safeguarding patient safety and product efficacy.
Why Choose EPiC for your GXP Training & Education
Our team comprises former regulatory inspectors with extensive experience in the pharmaceutical industry. This unique perspective allows us to provide insights and guidance that are both practical and aligned with current regulatory expectations. Our trainers have first-hand knowledge of what inspectors look for during audits and inspections, ensuring that your team is well-prepared. EPiC offers a wide range of training programs tailored to meet the specific needs of your organisation.
Next Steps
Ready to elevate your GXP compliance efforts? Contact EPiC today to learn more about our training programs and how we can support your organisation’s compliance journey.