eRISE Conference
- powered by eRA & ePI Summit

11-12 May 2027 | Munich, Germany

Where Health Authorities, Industry, and Healthcare Professionals Connect to Explore the Future of Life Sciences Information

Perfect networking opportunity for industry and agency experts

2 Days full of presentations, break-out sessions and user group meetings

Exclusive evening event as part of the conference ticket

eRISE: electronic Regulated Information & Smart Ecosystems Conference

Welcome to eRISE, the premier platform powered by eRA and ePI Summit, bringing together health authority representatives, industry leaders and healthcare professionals to connect, learn, and share a common stage.

For many years, our eRA Conference has been a trusted forum for regulatory professionals, known for its strong community, practical discussions, and high-quality content. Building on this success, we are happy to expand the conversation: In 2027, the eRA Conference, in collaboration with cormeo, will join forces with the ePI Summit to create eRISE.

By bringing together health authorities, industry leaders, and healthcare professionals, eRISE creates new opportunities to explore the future of regulated information, exchange perspectives, and address shared challenges across the life sciences landscape.

While the scope is broadening, the foundations remain the same: The expert-led content, collaborative atmosphere, and strong sense of community that have defined the eRA Conference will continue to be at the heart of the event.

Rooted in the eRA experience. Expanded through new perspectives. Welcome to eRISE.

Visit the event website

Who should attend?

eRISE offers participants a unique mix of expertise, perspectives, and solutions, connecting the entire regulated information lifecycle from submission to patient. Created and realized by cormeo, eRISE connects customers, partners, and friends of EXTEDO, Docuvera, Rote Liste, and medicines.ie.
Thus, attendees gain access to a wide range of discussions and expert presentations covering the creation, management, and distribution of regulated information as well as the latest important developments like electronic product information (ePI), eCTD v4, or cloud-based regulated spaces (CRS). Whether you’re deep in regulatory submissions, shaping the next generation of patient information, or exploring how AI and structured data will transform the industry, at eRISE you will be where these worlds meet.

Organizations

Life sciences companies: originator and generic pharmaceutical companies, biotech firms, marketing authorization holders, and CROs that create, manage, and submit regulatory content and product information
Regulatory authorities: national and international regulators shaping data standards such as ePI and eCTD, and their implementation
Industry associations: organizations representing the interests of the pharmaceutical industry and contributing to the development and adoption of standards
Compendia & medicines information providers: organizations that curate, publish, and distribute trusted medicines information to healthcare professionals and patients

Functions within these organizations:

Regulatory Affairs & Operations
Product Information & Labelling
Medical Writing & Medical Affairs
Quality
Drug Safety / Pharmacovigilance
Clinical
CMC (Chemistry, Manufacturing & Controls)
Other functions working with regulated information: specialists dealing with data standards such as eCTD, ePI, FHIR, and IDMP, including data management and digital and process owners

Asphalion is a leading international provider of scientific, regulatory, and safety consulting solutions in the life sciences sector, with over 25 years of experience.

We offer strategic advice, expert consulting, operational support, and full outsourcing services for all types of products in every therapeutic area, covering non-clinical and clinical development, CMC, dossier writing, regulatory procedures, vigilance, eSubmissions and data management for pharma, biopharma and medical devices clients.

Asphalion has a team of 20+ members devoted to Data Management and eSubmission that uses the latest regulatory intelligence technologies to help Pharma and MedTech companies align internal processes and information. Our experts work together with key stakeholders, delivering successful, high-quality results.

Our Data Management Unit helps Pharma and MedTech companies sort existing data to generate a unique source of true, compliant with ISO IDMP, NVR or EUDAMED standards, facilitating alignment of internal processes and information. Our subject matter experts work together with EMA and other regulatory stakeholders, what results in successful, high-quality results.