Asphalion Knowledge Centre

Asphalion Knowledge Centre is a leading online training platform for Biotech, Pharma, and Medtech professionals. It offers specialized courses taught by expert trainers familiar with EU and US regulations, ensuring a relevant learning experience. Courses cater to diverse learner needs, enabling flexible, self-paced learning worldwide. The center is committed to promoting continuous learning and professional excellence. 

Explore our courses and contact us for guidance.

Curso Ctis Asphalion Knowledge Centre

Advanced training on the Clinical Trials Information System (CTIS)

Discover the keys to successful CTIS portal management and learn its key functionalities through this comprehensive course, featuring live demonstrations and expert guidance.
Date: September 17
English |
Online
Internal Auditors Iso 13485

Internal Auditors ISO 13485

Unlock ISO 13485:2016 auditing expertise. Master compliance, audit essentials, and boost your medical device quality management skills.
Dates TBD
English |
Online
Key Points In The Elaboration Of Psurs For Medicinal Products And Medical Devices

Key points in the elaboration of PSURS for medicinal products and medical devices

Master the art of PSURs: Unveil the safety and efficacy of medical products through expert-led analysis and risk assessment.
Dates TBD
Spanish |
Online
Elaboration Of Safety Management Plan For Clinical Trials

Elaboration of safety management plan for clinical trials: key points and recommendations

Ensure trial safety with precision: Craft a robust Safety Management Plan to safeguard participants and ensure regulatory alignment.
Dates TBD
English |
Online
Quality Management System In Compliance With Iso 13485

Establishment of a Quality Management System in compliance with ISO 13485

Learn ISO 13485:2016 Quality Management Systems. Implement, maintain, and certify compliance. Two 4-hour sessions for medical device professionals.
Dates TBD
English |
Online
Pharmacovigilance System Implementation By Sme Mah

Pharmacovigilance system implementation by SME MAH. Challenges and recomendations.

Navigate PV compliance with ease: Tailored strategies for SME MAHs to optimize safety and streamline operations.
Dates TBD
Spanish |
Online
Post-Marketing Surveillance According To Mdr Regulation

Post-Marketing Surveillance (PMS) according to MDR regulation: key points and challenges

Stay ahead in medical device safety: Master the MDR’s PMS requirements to excel in market surveillance and patient care.
Dates TBD
English |
Online
Pharmacovigilance Literature Searches In The Digital Age

Pharmacovigilance literature searches in the digital age

Empower your pharmacovigilance with digital-age strategies for literature searches – stay compliant and informed!
Dates TBD
Spanish |
Online
Fundamentals For Clinical Affairs

Fundamentals for Clinical Affairs

Explore Fundamental Clinical Affairs for Medical Devices: Ensure Compliance and Patient Safety with Expert Guidance.
Dates TBD
English |
Online
Borderline And Classification Of Medical Devices

Borderline and Classification of medical devices

Learn to classify medical devices in compliance with EU regulations. Understand borderline cases. 4-hour session for medical device professionals and developers.
Dates TBD
English |
Online
Medical Device Risk Management

Fundamentals for medical device Risk Management

Gain insights into ISO 14971:2019-compliant medical device risk management. Understand risk assessment, control, and safety compliance in the product lifecycle.
Dates TBD
English |
Online
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As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.

Memberships & PartnershipS

Catalonia.health
Catalonia Trade & Investment - ACCIÓ
Team PRRC
Veeva Certified Partner
Navarra Health Cluster
Cluster MAD eHealth

Quality Management System

Innovative SME

SDGs

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As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.

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