A white background with a few lines on it

Circle Life Sciences Resource Library

Circle LifeSciences as part of CSR Group has a community of over 30,000 people, and we gather exclusive insights and reports for the Pharma world.

Dive into all our resources for free!

Industry Insights

Free Resources

Job Descriptions

Community Access

The looming shadow of the QP Talent Gap

The pharmaceutical industry faces a looming crisis: a significant shortage of qualified persons (QPs). This crucial role, responsible for ensuring the quality, safety, and compliance of medicines, is experiencing a growing demand that outpaces supply. This report delves into the factors contributing to this shortage, its potential consequences, and proposes solutions to ensure a sustainable future for the pharmaceutical industry and, ultimately, patient safety.Dive into the industry challenges, insights and more around the QP talent shortage and how best to address this

Dowload now

A person is holding a book titled the learning shadow of a talent gap.

A person is holding a tablet that says `` is your pharmaceutical business in regulatory remediation ? ''

Are regulatory pressures threatening your business?

Navigating the complexities of regulatory remediation can be daunting, time-consuming, and costly. The stakes are high—facing potential production shutdowns, costly recalls, legal penalties, and damage to your company’s reputation. But it doesn't have to be this way.

Download our free help guide now

Empowering the Next Generation:The Role of Experienced QPs as Mentors

In the pharmaceutical industry, the role of Qualified Persons (QPs) is crucial in ensuring product quality and regulatory compliance.

However, newly qualified QPs often face significant challenges in transitioning from academic knowledge to practical application.

This white paper highlights the successful implementation of our structured mentorship programme for new QPs, utilising experienced QP contractors as mentors.

Download our free help guide now

A book titled empowering the next generation : the role of experienced qps as mentors

A brochure about how contractors can support uk ops in meeting mhra documentation requirements.

How Contractors Can Support UK QPs in Meeting MHRA Documentation Requirements?

In the ever-evolving landscape of clinical research, the UK's regulatory framework for clinical trials continues to present both challenges and opportunities for Contract Research Organisations (CROs). A significant aspect of this framework involves the documentation requirements set forth by the Medicines and Healthcare products Regulatory Agency (MHRA) for Qualified Persons (QPs) under the UK's MIA(IMP) licences. For CROs operating in the UK, ensuring compliance with these documentation requirements is crucial for the successful import of Investigational Medicinal Products (IMPs) into Great Britain.

Download our free resource now

Trusted to Power