Staying up to date with Regulation, Signal and Risk Management during the Covid-19 Pandemic
October 8th–9th, 2020
As Pharmacovigilance systems are changing significantly around the world, it is very important companies remain updated at all times. Adding to this the rising demand for drugs, the amplified need for novel therapeutics development via extensive clinical trials and the world population growth made drug manufacturers to start to pay more attention to Pharmacovigilance field as public anxiety about safety increases.
Furthermore the growth of artificial intelligence and combination products, signal management is ever more important. It is important to meet the right people and understand the regulatory changes with IDMP, combo products as well as being prepared for inspections and audits.
On this B2B event participants will have the chance to learn more about this challenging era and the latest developments in Pharmacovigilance and Drug Safety with the main key players in this field.
This event will be focusing on trends on Regulatory Challenges, Signal Detection, Data Management, Risk management, Audit & Inspection and New Technology applied to Pharmacovigilance procedures.
We invite you to discuss and debate these challenges in a dialogue amongst top professionals in Pharmacovigilance.
Impacts of PV on Covid-19
Improving Signal surveillance
Artificial Intelligence in Signal Detection
Combination products – Regulation, trials, and risk management
The role of data mining in Pharmacovigilance and its benefits
IDMP standards and strategy
Developing a pharmacovigilance risk management plan with a risk minimization action plan (RiskMAP) for high risk products
Understanding how Artificial Intelligence is transforming pharmacovigilance
Evaluation of quality and manufacturing in production
Audits and Inspections
Strengthening Pharmacovigilance quality management system
Impact of AI in Pharmacovigilance
Upcoming regulatory changes
Application of data analytics in Pharmacovigilance processes to increase speed of signal detection
Who Should Attend:
CEOs / Presidents / MDs, CCOs/CMOs/CDOs, Chief Executives, Directors, Vice Presidents, Department Heads, Leaders, and Managers specialising in:
Assurance & Compliance
Clinical Data Management
Adverse Drug Reactions
Clinical Trial Management
Research & Development
Regulatory Affairs and Compliance
Data management and data mining
PV Inspection and Audit Readiness
Patient Support Programs
Medical Product Safety Assessment
Phase IV/Postmarketing Safety
International and regional health authorities and regulators
Clinical Research Organization (CRO) service providers
Business Process Outsourcing (BPO) service providers
Risk Management Software developers
Pharmacovigilance Audit Firm’s
Pharmacovigilance consultancy service providers
Contract Research Organizations
Adverse Event/Case Management Service Providers
Safety Database Providers for Case Management
Healthcare Translation Agencies
Technology Vendors/Portal Service Provider
For any enquiry on regards to special offers & group discounts please contact us directly at: email@example.com
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