QUALITY. ASSURED.
Invest in quality to promote a culture of confidence
Our team provides a wealth of experience from a variety of backgrounds, with specialist insight to complement a range of areas. Client focussed, dedicated and knowledgeable you can rely on JensonR+ to provide a thorough and complete quality and compliance service.
Reassuringly diligent.
Our team can ensure your quality system is tailored, robust and compliant.
Boasting trained auditors and compliance system experts our eye for detail will ensure a robust system and quality focus.
From the fine details to the big ideas JensonR+ has got you covered.
OUR TEAM
Specialised and experienced
Our specialist team is experienced in Good Distribution Practice (GDP), Good Manufacturing Practice (GMP) Good documentation Practice, Compliance for Medical Devices and Medicines. As well as Quality Assurance, Quality Management Systems, Project coordination and management, Auditing and delivering high-quality training. Our RPs adhere to the Cogent Gold Standard and we work to GxP Industry Standards to maintain quality systems. Our talented Auditors have also completed and passed the CQI and IRCA certified (QMS) Lead Auditor Course.
Great experience working with JensonR+, especially Chloe. Very professional, organised and friendly support from day one to the completion of contract. I found their understanding of GDP and Quality systems are best in the Pharma and Biopharma industry. Good thing with JRP is that they have all the departments and come very handy if the client need arises.
Chloe Child is very knowledgeable and an experience Quality Person. She is approachable and a hardworking professional.
Chloe led our MHRA session very well and we had a good outcome despite it being announced within two weeks of her assignment. She followed up the inspection with a remediation plan implemented it meticulously within the stipulated timeframe. She keeps up-to-date with GDP knowledge, learns about the problems within the industry and quickly applies it to the client to avoid compliance issue and keep to current GDP.
Read the latest updates from our Quality Team
Inspections
The Quality Team at JensonR+ have been incredibly busy, with three successful MHRA GDP inspections in as many days, one routine inspection and two new applications, for our clients.
Introducing Mark King
Introducing Mark King,
our new Associate Director of […]
First IMP Batch
We’re pleased to announce that our team at JensonR+ have released our first Investigational Medicinal Products (IMP) batch. Our quality team have made the final sign-off marking the culmination of the quality process through which a batch of IMP has been shown to conform to all aspects of Good Manufacturing Practice (GMP).
MHRA Compliance Monitor (CM) programme – Inspection readiness – Part 2
From April 2022 the MHRA will be introducing a programme to improve the supervision of appropriate companies who are at Inspection Action Group (IAG) stage to assist with inspection readiness.