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News - Why I Value Attending PFS & Injectable Drug Devices Europe

December 2025 | Fatima Sanfourche, Global Senior Director for QA & RA Compliance, Medical Devices, Combination Products & eHealth, Bayer


As an Advisory Board member and speaker at the PFS Europe Conference, I see this event as an opportunity to stay informed and connected within the evolving field of injectable drug delivery. The industry faces complex challenges, from regulatory requirements to sustainability considerations, and having a forum to discuss these openly is important.


I attend because the conference provides a space for practical dialogue. It’s not just about presentations; it’s about listening to different perspectives and understanding how others approach similar issues. These conversations often highlight trends and solutions that might not be immediately visible in day-to-day work.


What do I take away from the experience? Primarily, a broader view. Hearing from professionals across pharma, biotech, and device development helps me understand where the sector is heading and what that means for patient safety and product design. It’s also a chance to reflect on how we can improve processes collectively rather than in isolation.


Networking is another aspect I value. Meeting peers and exchanging ideas in person often leads to collaborations or simply a better appreciation of the challenges others face. These interactions make the work feel less siloed and more connected.


This year, I will be presenting on “Navigating Global Compliance and Sustainability Mandates: Strategies for Aligning with Evolving Regulations and Regional Variations.” My session will explore compliance challenges, sustainability mandates in the pharmaceutical industry, and practical strategies for integrating these considerations into regulatory planning.


For me, PFS Europe is about learning and contributing to discussions that matter. It’s a chance to share experiences, gain insights, and return to work, for 2026, with a clearer sense of the bigger picture.


About the Author
Fatima Sanfourche is an experienced regulatory affairs professional with a strong focus on compliance in pharmaceutical development. As an Advisory Board member for PFS Europe, Fatima brings extensive expertise in navigating global regulatory frameworks and supporting innovation in drug-device combination products.
 



WHAT IS CPD?

CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

CPD AND PROFESSIONAL INSTITUTES

There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

GLOBAL CPD

Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

CPD Certificates

We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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