Global Pharmaceutical Consultants GXP Consultancy

Contract QP, RP, RPI and Compliance Monitor Services

Contract QP, RP, and RPi Services

EPiC has consultants within our consortium of ex Regulatory experts who are eligible to act as Contract Qualified Person (QP), Responsible Person (RP) and Responsible Person (import) (RPi) and can provide contract QP, RP, and RPi services to support holders of Manufacturing and Import authorisations and Wholesale Distribution Authorisation holders to meet the legal obligations as a licence holder.

contract qp rp and compliance monitor services

In addition to exercising due diligence to ensure compliance with applicable regulatory requirements and published guidance, our consultants have the added benefit of being able to provide expert advice on technical and quality issues adding value and mentorship to develop inhouse Quality Assurance knowledge and capabilities.

Compliance Monitor

A number of consultants working for EPiC have been deemed eligible by the MHRA to act as Compliance Monitors (CM) in MHRA’s pilot compliance monitor programme for GMP/GDP remediation supervision activities.

We provide experienced and qualified personnel to support you in meeting your regulatory obligations. Many of our consultants are eligible to be named on Manufacturing and Wholesale Dealer Licences and a number are eligible to act as Compliance Monitors. 

We regularly support companies who have been referred to CMT or IAG, leading root cause analysis workshops, advising on the response to the inspection findings, developing remediation plans, and assisting with implementation.

Why Choose EPiC for Contract QP, RP, and RPi Services

Our team of former inspectors and industry experts brings a wealth of experience and knowledge, and many of our consultants are eligible to be named as Contract Qualified Person (QP), Responsible Person (RP), and Responsible Person (import) (RPi) on licenses.

By contracting EPiC to provide these services, you will not only meet your regulatory obligations but also benefit from valuable insights into technical and quality issues, enhancing your company’s in-house Quality Assurance knowledge and capabilities.

Additionally, our consultants, who are eligible to act as Compliance Monitors in MHRA’s pilot program, have extensive experience in MHRA Compliance Management Team (CMT) and Inspection Action Group (IAG) processes, making EPiC well-equipped to support your post-inspection remediation needs.

Next Steps

Ready to ensure your compliance with regulatory requirements and enhance your quality assurance capabilities? Contact EPiC today to learn more about our Contract QP, RP, and RPi services. Our team of ex-regulatory experts are here to support you in meeting your legal obligations and providing valuable mentorship.

Additionally, take advantage of our Compliance Monitor services for GMP/GDP remediation supervision. Let EPiC guide you through post-inspection remediation with expert advice and comprehensive support.