Providing the key link between pharmaceutical companies and regulating bodies, we work to ensure life-saving treatments and diagnostics are delivered to patients in a safe and timely manner. Guiding and advising our clients, we are involved in every stage of bringing medicines and medical devices to global markets.

MEANINGFUL

We are involved in countless meaningful projects that bring positive change to science – offering new cutting-edge and life-changing medicine and medical devices for patients and medical experts worldwide.

FAMILY

We are a close-knit and growing team of passionate individuals who recognise each other’s achievements and help one another grow. Each with different fields of knowledge and interests - but unified by a thirst for regulatory affairs.

Here at RApport, our people are our greatest asset.

GROWTH

We encourage our team constantly learn, by supporting employee-led development in the direction of their choice. Offering funding for training and apprenticeship programs, RApport is keen to support individual growth and success. Regularly offering opportunities for career development, we will encourage you in any direction you want to go. To learn more about who we are, please visit rapportss.com

Hear from our employees - 

"At RApport, I have gained the confidence to achieve beyond my expectations. The ongoing guidance from my team and regular training sessions have enabled me to challenge myself, utilising my knowledge to support and lead client projects. It is clear to me that whatever career development pathway I choose whether it be project managing a brand marketing campaign or learning about cosmetic regulatory, I will be supported and encouraged throughout my entire career." - Lauren Nickson, Regulatory Affairs Officer

"When I first started working at RApport, I came from a physics background and was new to the world of regulatory. However, the support I have received for my career growth has been exceptional. Last year, I was given the opportunity to train in medical devices and even received my Green Belt certification. This has opened up a whole new world of medical devices, their requirements, and regulations for me. In a short period of time, I have been involved in carrying out Gap Assessments for Quality Management Systems, creating QMS systems for many clients, and making them ISO 13585 and EU MDR compliant.

RApport offers significant prospects for career development and advancement. Regular mentoring sessions with my manager have proven to be highly beneficial for professional growth. Working at RApport provides exposure to multiple projects related to CMC, regulatory strategy, labelling, and other areas of Regulatory Affairs, facilitating exploration of diverse career paths and specialisations.

I am grateful to be working with an amazing, supportive team and brilliant leadership. I am looking forward to exciting future ventures!" - Maryam Tahoor, Regulatory Affairs Officer