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
More great feedback for our Quality team
We pride ourselves on providing an exceptional service to our clients, but you don’t just have to take our word for it. Read what one of our clients had to say about working with our Quality team...
EMA and PIC/s Issue Concept Paper for GMP Annex 11 (Computer Systems)
A 5-page concept paper was issued by the European Medicines Association (EMA) and Pharmaceutical Inspection Co-operation Scheme (PIC/s) on 16th November 2022 with a deadline for comments by 16th January 2023.
Another happy Jenson client
We pride ourselves on being responsive to our clients and incorporate feedback into our activities. Nobody can tell you about our services better than our clients, so we’re happy to share some recent feedback that we received following a project that one of our RPs Chloe Child worked on.
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.