Staying ahead in the ever-evolving world of Medical Device and Pharmaceutical Regulations is crucial to the success of every medical device and pharmaceutical company. The constant changes and updates can be overwhelming, making it challenging for professionals to stay informed and adapt to the new regulatory landscape.
At our exclusive webinar, we bring you the opportunity to dive deep into the most important regulatory updates of 2023 that impact medical device and pharmaceutical companies. Led by our expert presenter, Martin King, who brings over 40 years of global experience in the industry, we’ll provide you with invaluable insights and guidance.
Join us for the Important Regulatory Highlights for Pharma and Medtech for 2023/24 webinar, where we will equip you with the knowledge you need to navigate the regulatory challenges in the upcoming year. Whether you’re a seasoned professional or new to the field, this webinar is designed to empower you with the latest information and industry trends.
Who Should Attend:
All levels with regulatory interest in Pharmaceuticals and Medical Device
- Skill Level: Novice, Intermediate , Expert
By attending this webinar, you will:
- Gain an overview of the highlights of 2023 that impact the pharmaceutical and medical device regulatory landscape.
- Understand the regulatory shifts and industry innovations to expect in 2024.
- Acquire the knowledge you need to stay ahead and succeed in your daily business operations.
- Get a chance to engage with our expert during the Q&A session
Don’t miss out on this valuable opportunity to stay informed and gain a competitive edge!
Special event information:
Live attendees will receive a complimentary certificate of attendance.
Martin KingQA/RA Business Enabler
Martin brings extensive global experience from working throughout the life-science Pharmaceuticals and Medical device value chain. His strong business acumen and diverse technical engineering background has guided him through a 40+ year career with Medical Devices and Pharmaceuticals. He has executed successful Regulatory Submissions on 6 of the seven continents.
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If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days.
Yes, our event partners will email you the event recording within several weeks.