Search
Close this search box.
Logo Asphalion

News and Events

Stay in touch with the latest news and upcoming events featuring Asphalion

Andre Mota New Operations Director 3

New Consultancy Operations Director | André Mota

Good news at Asphalion! We are thrilled to announce that André Mota has been appointed Consultancy Operations Director! André holds a Pharmacist Degree and has pursued postgraduate studies in Pharmaceutical Technology, alongside a comprehensive training program in business management. As a Regulatory Affairs Expert, his proficiency spans across various domains, including the quality of human medicinal products, regulatory affairs management, and project management. Previously, André has excelled in roles such as RA Director for CMC & Life-Cycle Management, where he demonstrated exceptional leadership and strategic planning skills. As he says, “I’m excited to embrace this new challenge and to step

More News & Events

High Risk Medical Devices Pilot Ema

NEWS | High-risk medical devices pilot

EMA has launched a pilot to give scientific advice on the intended clinical development strategy and proposals for clinical investigation for certain high-risk medical devices.

More +
Timeline Pms Journey

EVENT | EMA PMS Info Day

EMA is holding a new public event with the purpose to provide a comprehensive understanding of Product Management Service (PMS) and its implications on other EMA digital services with the objective to introduce the core concepts of PMS, ensuring that all attendees have the chance to understand its implementation.

More +
20Th Biosimilars Conference

EVENT | 20th Biosimilar Medicines Conference by MFE

During these two interactive days, actors of the healthcare community alongside world experts in biosimilar medicines will gather and debate the evolving biosimilar medicines landscape and emerging trends. Discussion will focus on sharing good practices and setting collective aims to achieve the depth, breadth and speed of the use of biosimilar medicines as a lever to untap their transformative value.

More +
New Insight On The Implementation Of Mdr Article 17

NEWS | New Insight on the Implementation of MDR Article 17

Article 17 of Regulation (EU) 2017/745 (Medical Device Regulation – MDR) regulates the reprocessing of single-use devices (SUDs) with relevance for the European Economic Area (EEA) which may only take place where permitted by national law and in accordance with this article.

More +

Search or filter

  • Filter by category

Schedule a Free Meeting

Schedule here a free 30-minutes meeting with one of our consultants and tell us about your project, challenges or doubts. 

We will be happy to assist you!

Schedule a meeting