Continuously parsing official EU and national health policy sources via structured and unstructured feeds, normalizing data into a unified, queryable index.
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EMA - European Medicines Agency
Centralized drug authorizations and pharmacovigilance updates
EMA Regulatory Guidelines
Clinical trial protocols, GMP standards, and regulatory procedures
EC Public Health
Regulatory developments and compliance requirements
EC Digital Health
Regulatory developments and compliance requirements
EC AI Act & Regulation
Regulatory developments and compliance requirements
EC Data Strategy
Regulatory developments and compliance requirements
European Health Data Space
Regulatory developments and compliance requirements
EC Pharmaceutical Strategy
Regulatory developments and compliance requirements
EC Medical Devices
Regulatory developments and compliance requirements
EC Clinical Trials
Regulatory developments and compliance requirements
EUR-Lex Official Journal
EU directives, regulations, and implementing acts in healthcare
EUnetHTA 21
Regulatory developments and compliance requirements
Heads of Medicines Agencies
Regulatory developments and compliance requirements
EUDAMED
Regulatory developments and compliance requirements
Clinical Trials Information System (CTIS)
Regulatory developments and compliance requirements
EDQM - European Pharmacopoeia
European Pharmacopoeia standards and quality control
EC Competition - Pharma Sector
Regulatory developments and compliance requirements
UK MHRA
UK pharmaceutical licensing and post-market surveillance
UK NICE
Cost-effectiveness assessments and clinical practice guidelines
UK DHSC
UK health policy statements, consultations, and impact assessments
UK Drug Safety Update
Regulatory developments and compliance requirements
UK Care Quality Commission
Regulatory developments and compliance requirements
NHS Digital/England
NHS app updates, digital transformation, and data standards
UK Health Research Authority
Regulatory developments and compliance requirements
NHS Transformation Directorate
Service changes, clinical guidelines, and commissioning policies
UK ICO - Health Sector
Regulatory developments and compliance requirements
Scottish Medicines Consortium
Regulatory developments and compliance requirements
BfArM (Federal Institute for Drugs)
German drug approvals, clinical trial authorizations, and risk assessments
BfArM DiGA Fast Track
German drug approvals, clinical trial authorizations, and risk assessments
German Federal Ministry of Health
Regulatory developments and compliance requirements
gematik (German Digital Health)
E-prescription standards, health card updates, and telematics infrastructure
IQWiG (German HTA)
Regulatory developments and compliance requirements
G-BA (Federal Joint Committee)
German benefit assessments and reimbursement decisions
Paul-Ehrlich-Institut
Vaccine approvals and blood product regulations in Germany
BSI - Healthcare Cybersecurity
Regulatory developments and compliance requirements
DIMDI Medical Device Database
Regulatory developments and compliance requirements
ANSM (French Medicine Agency)
French drug safety monitoring and clinical trial authorizations
Haute Autorité de Santé (HAS)
French drug reimbursement decisions and medical device evaluations
French Ministry of Health
French healthcare system reforms and public health campaigns
CNIL - Health Data
Regulatory developments and compliance requirements
ANS - French Digital Health Agency
Regulatory developments and compliance requirements
CEPS - Drug Pricing Committee
Regulatory developments and compliance requirements
AIFA (Italian Medicines Agency)
Regulatory developments and compliance requirements
Italian Ministry of Health
Regulatory developments and compliance requirements
Agenas - Italian HTA
Regulatory developments and compliance requirements
AEMPS (Spanish Medicine Agency)
Regulatory developments and compliance requirements
Spanish Ministry of Health
Regulatory developments and compliance requirements
Spanish Health Technology Institute
Regulatory developments and compliance requirements
CBG-MEB (Dutch Medicine Agency)
Dutch medicine evaluations and pharmacovigilance activities
Dutch Ministry of Health
Dutch healthcare insurance updates and quality standards
RIVM - Dutch Health Institute
Dutch public health research and vaccination programs
Zorginstituut Nederland
Regulatory developments and compliance requirements
FAMHP (Belgian Medicine Agency)
Belgian pharmaceutical oversight and clinical trial approvals
INAMI-RIZIV (Belgian HTA)
Regulatory developments and compliance requirements
Swissmedic
Swiss drug approvals and medical device certifications
Swiss Federal Office of Public Health
Regulatory developments and compliance requirements
Swedish Medical Products Agency
Regulatory developments and compliance requirements
TLV (Swedish HTA)
Regulatory developments and compliance requirements
Danish Medicines Agency
Regulatory developments and compliance requirements
NoMA (Norwegian Medicines Agency)
Regulatory developments and compliance requirements
EU HTA Regulation Implementation
Regulatory developments and compliance requirements
EU AI Act Implementation
Regulatory developments and compliance requirements
European Health Data Space
Regulatory developments and compliance requirements
MyHealth@EU Cross-Border Services
Regulatory developments and compliance requirements
HTA Coordination Group
Regulatory developments and compliance requirements
ACT EU - Accelerating Clinical Trials
Regulatory developments and compliance requirements