ICH
ICH Efficacy Guidelines — E2 Pharmacovigilance Series
The international E2 guideline family covering clinical safety data management and post-approval pharmacovigilance.
Open official page Free official-source directory
Go to the organization that owns the information.
Search direct links to official regulator, public-agency, standards-body, terminology, reporting-system, and safety-information pages.
52 official links16 regions coveredFree to use
Directory review11 August 2026
PiVily provides navigation and short functional descriptions. Linked content remains owned and maintained by the official source. The directory is reviewed quarterly.
Search the directory
Official pages across the PV ecosystem.
Use region and category filters or search for a regulator, system, standard, or topic. All results open the publisher's external website.
What you can searchRegulators · Standards · Reporting systems · Terminology · Guidance · Safety information
52 official links match
ICH / MedDRA MSSO
MedDRA
The standardized medical terminology used to support regulatory communication and safety-data exchange.
Open official page CIOMS
CIOMS Publications
Consensus reports and working-group publications spanning drug safety, benefit-risk, pharmacoepidemiology, and research ethics.
Open official page World Health Organization
WHO Pharmacovigilance
WHO's overview of global pharmacovigilance, safety monitoring, systems strengthening, and related networks.
Open official page World Health Organization
WHO Programme for International Drug Monitoring
The international framework connecting national pharmacovigilance centres for shared learning and signal detection.
Open official page World Health Organization
WHO Pharmacovigilance Collaborating Centres
A directory of collaborating centres supporting global pharmacovigilance capacity and technical work.
Open official page European Medicines Agency
Good Pharmacovigilance Practices (GVP)
The EU's modular guidance for the conduct of pharmacovigilance by marketing-authorisation holders and regulators.
Open official page European Medicines Agency
Pharmacovigilance Risk Assessment Committee (PRAC)
Committee agendas, minutes, meeting highlights, members, and documents for EU medicine-safety oversight.
Open official page European Medicines Agency
PRAC Recommendations on Safety Signals
Published recommendations arising from PRAC's assessment of safety signals for human medicines.
Open official page European Medicines Agency
EudraVigilance
The EU system for managing and analysing suspected adverse-reaction reports involving authorised medicines and clinical trials.
Open official page European Medicines Agency
Real-World Evidence at EMA
EMA resources describing the use of real-world data and evidence across regulatory decision-making.
Open official page Heads of Medicines Agencies
CMDh — Human Medicines
Coordination-group materials for mutual-recognition and decentralised procedures, including safety-related outcomes.
Open official page Continue with PiVily
Use the platform for what comes next.
Read the analysis, build context for your development, or learn through responsible peer exchange.
Structured request