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 QA+ 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 QA+ 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.
Sarah Chikhani
Head of Quality (GDP)
Read the latest updates from our Quality Team
Brexit Border Control and Tariff Update
The government have recently published a paper confirming their stance in relation to the border controls and tariffs to be placed between Ireland (EU) and Mainland UK (including Northern Ireland).
COVID-19 Transportation Legislation Update
COVID-19 has caused massive disruption to the transport industry with the number of passengers travelling between mainland UK, as well as Northern Ireland, and the EU is, at this current time, greatly diminished. Read more about the UK government's £35m investment to protect vital supplies that use these freight routes.
5 considerations for managing GDP risk and process changes during COVID-19
Disruption to the supply chain has given rise to difficulties for wholesalers in applying the safeguards in GDP to meet supply needs. Here we explain the temporary regulatory flexibilities that have been introduced to address the current exceptional circumstances.
Are you getting value from your PQR process?
Pharmaceutical companies and in particular small to medium sized ones, are in a perpetual battle to increase efficiency and reduce costs while staying GMP compliant. The always moving landscape of regulatory compliance puts significant demands on the sometimes-limited resources available to these companies. This can result in the prioritisation of activities of seemingly more importance which will inevitably, despite best efforts, lead to the neglect of others.
We would like to talk to you and we will listen.
We aim to understand your objectives, your aspirations and your ultimate goals.