FAQs

We work with individual clinical research professionals and organisations involved in the development, management, conduct and oversight of clinical research. Our clients include pharmaceutical and biotechnology companies, medical device manufacturers, sponsors, contract research organisations (CROs), research sites, healthcare organisations and emerging life science businesses.

Our flexible services can support a single learner, a growing research team or an international organisation requiring training or consultancy across multiple functions.

Our clinical training is created by experienced subject-matter experts who understand how regulatory requirements apply in real research environments. We focus on explaining not only what the requirements say, but why they matter and how they influence day-to-day clinical practice.

Courses are designed to be clear, engaging and scientifically grounded, using practical explanations and interactive learning to move beyond a purely “tick-box” approach to compliance training.

Integrity’s courses are developed and reviewed by clinical research and training professionals with relevant industry experience. Their practical knowledge helps ensure that course content is accurate, understandable and applicable to the responsibilities learners face in real clinical research settings.

Our courses are regularly reviewed and updated when relevant regulations, standards or recognised industry guidance change. The applicable course page will identify the framework or version covered, helping individuals and organisations select training aligned with their current requirements.

GCP training is relevant to people whose work affects the conduct, management, oversight or reporting of clinical research. This may include investigators, research nurses, study coordinators, clinical project managers, clinical research associates and monitors, sponsor and CRO teams, quality assurance professionals, medical writers, data management teams and regulatory affairs personnel.

The appropriate training should reflect the individual’s role, responsibilities, study type and the regulations or standards applicable to the research.

Integrity Clinical Compliance provides GCP training through self-paced online courses, and bespoke corporate programmes. Our training portfolio includes courses addressing important clinical research requirements, including ICH Good Clinical Practice E6(R3) and ISO 14155:2026 for medical device clinical investigations.

Please visit our online course catalogue for the latest available courses and the standards covered by each programme.

ICH GCP E6(R3) provides an international Good Clinical Practice framework for clinical trials of investigational products. ISO 14155:2026 is the international Good Clinical Practice standard specifically addressing clinical investigations of medical devices involving human participants.

The right course therefore depends on the type of clinical research you conduct and your responsibilities within it. Some professionals and organisations may need training in both frameworks. Integrity can help you identify the most appropriate training for your team.

Yes. All of our courses allow learners to complete training flexibly from a suitable computer or device. Courses are self-paced, enabling learners to work through the content around their professional commitments and revisit material when needed during their access period.

We also provide tailored corporate training for organisations that require team-based learning.

There is no single refresher interval that is appropriate for every role or organisation. Refresher training should take account of applicable regulations and guidance, sponsor or employer requirements, internal procedures, changes to a person’s responsibilities and significant updates to GCP standards.

Many organisations set their own defined refresher cycle, usually every 2 years, and require additional training when important regulatory changes occur. Integrity can support organisations in reviewing their training needs and identifying potential knowledge gaps.

Yes. Integrity provides training relevant to pharmaceutical, biotechnology and medical device research. Because different frameworks can apply, learners should select the course that matches their research type and responsibilities; for example, ICH GCP E6(R3) training for applicable clinical trials or ISO 14155:2026 training for medical device clinical investigations.

All our online courses include an assessment. Assessment and pass requirements vary between courses and will be explained within the relevant course information and learning programme.

Completion time varies according to the subject, depth of content, learner’s pace and how many of the additional resources you choose to access. The estimated duration is provided on the individual course page. As courses are self-paced, learners can work through the material in a way that suits their existing knowledge and professional commitments.

Unless stated otherwise on the relevant course page or purchasing agreement, online courses are available for up to two years from enrolment. The course must be completed within the applicable access period to receive a completion certificate.

Corporate access arrangements may differ where they form part of an agreed training package.

Yes. Integrity’s flexible online courses are designed to be completed at your own pace. You can pause your learning and return during the course access period, making the training easier to fit around work and other commitments.

Yes. Integrity’s online courses can be translated into 32 different languages, making specialist clinical and Good Clinical Practice training more accessible to learners around the world. This allows individual learners to access course content in their preferred available language and helps international organisations deliver more consistent training across multilingual teams.

Please check the relevant course information or contact us to confirm the languages available for the course you wish to take.

Yes. Integrity Clinical Compliance retains appropriate course completion records. You or your employer can contact us to verify the validity of a certificate, subject to the necessary identity and data protection checks.

Completing relevant training can demonstrate professional development and help you build knowledge of clinical research requirements, but it does not guarantee employment. Your course certificate and course information can be added to your professional training record or portfolio as evidence of learning.

Employers may also consider relevant experience, qualifications, competencies and role-specific requirements when recruiting.

Select the course you require from our online clinical courses page and follow the registration and secure checkout process. Available payment methods are shown during checkout.

If you need licences for multiple learners, bespoke content or delivery through your organisation’s LMS, please contact us before purchasing so we can recommend the most suitable option.

We want learners to be satisfied with their training. Refund eligibility depends on factors including when the course was purchased, whether it has been accessed or completed and whether a certificate has been issued. Please contact us if you experience any issues or problems accessing your course.

Corporate pricing may be available when an organisation purchases licences for multiple learners. Pricing depends on the selected course, number of users, access requirements and any reporting, customisation or delivery needs. Please contact us for a tailored quotation.

Yes. We can create bespoke clinical and GCP training that reflects your organisation’s SOPs, processes, terminology, study types, therapeutic areas, risk profile and learner responsibilities. Bespoke training can focus on the practical situations your teams encounter rather than relying solely on generic compliance content.

Yes. A training gap analysis can help identify the knowledge and competency requirements associated with particular roles, processes and regulatory responsibilities. Integrity can review your current training arrangements, identify potential gaps and help you develop a more structured and proportionate training approach.

Yes. We provide white-label clinical training courses that can be prepared for delivery through an organisation’s existing Learning Management System, subject to technical compatibility and the agreed project scope. This can reduce the internal time and resources required to build specialist clinical compliance training from the beginning.

Courses can also be adapted to reflect your branding and organisational requirements.

Progress and completion arrangements depend on the course platform and corporate package selected. We can discuss learner enrolment, completion records, certificate verification and any reporting requirements when preparing your corporate training proposal.

Contact Integrity Clinical Compliance with the course or subject required, approximate number of learners, preferred delivery format and target completion date. Please also tell us whether you require bespoke content, reporting, branding or integration with your LMS. We will review your needs and recommend a suitable solution.

We support sponsors, pharmaceutical and biotechnology companies, medical device businesses, CROs, research organisations and emerging life science companies. Our consultancy can be scaled to suit established organisations as well as smaller businesses that may not yet have all the required clinical expertise in-house.

Yes. Integrity can provide targeted specialist input, additional operational capacity or structured oversight for a defined period or project. We will discuss the scope, deliverables, timescale and expertise required before recommending an appropriate consultant or support model.

Yes. Our quality assurance support can help organisations assess readiness, review relevant changes to systems, records and documentation (including electronic records), identify potential gaps and prepare teams for audit or inspection activity. The exact approach will depend on your organisation, study portfolio, responsibilities and the applicable regulatory framework.

Yes. Integrity provides medical writing, quality control and document review support for clinical research organisations. We can discuss the document type, intended audience, applicable requirements, development stage and required timescale to define the appropriate scope of work.

Yes. Emerging life science companies often require experienced clinical input before they are ready to build every capability internally. Integrity can provide flexible support with clinical operations, quality, training, documentation and project oversight, helping growing businesses establish practical and compliant ways of working.

Contact Integrity Clinical Compliance with a brief description of your organisation, project, current challenge, required timescale and the type of support you believe you need. If the precise requirement is not yet clear, we can arrange an initial discussion to explore your priorities and define an appropriate scope.