Pharmacovigilance managers and PV professionals with a number of years of experience.
This interactive course will cover the following subjects:
PV isn’t always black and white
PV interaction with Quality
Signals to Safety Variations
Pharmacovigilance System Master File and its challenges
Third party agreements
Risk management
UK Updates
Key Performance Indicators workshop
Discussion/Questions
Target audience:
Pharmacovigilance managers and PV professionals with a number of years of experience.
PIPA is a membership association for professionals working within the fields of medical information, pharmacovigilance and related functions in the pharmaceutical industry.
PIPA provides training, events, guidance, resources and networking opportunities to assist our members in their roles.
Background
During the early 1970’s information officers within the UK pharmaceutical industry identified areas of common interest and became increasingly aware of the need to exchange ideas and experiences to further their professional development. As a result, the Association of Information Officers in the Pharmaceutical Industry (AIOPI) was formed in 1974.
In 2005, AIOPI rebranded to PIPA in recognition of the growing number of members working within the field of pharmacovigilance.
PIPA’s membership now includes professionals who work in a variety of pharmaceutical information management roles, from entry level through to senior management:
medical information
pharmacovigilance
Code compliance
medical affairs
medical scientific liaison
regulatory affairs
scientific research information
business information
A growing number of members come from pharmaceutical companies outside the UK and from agencies, consultancies and service providers.
Aims
PIPA aims to:
provide a forum for the exchange of experience and the advancement of all aspects of medical, scientific and technical information handling relating to the pharmaceutical industry
facilitate friendly communication amongst those who have a special interest in this subject
encourage the maintenance and development of professional standards in all aspects of medical information and pharmacovigilance work
encourage and facilitate the development of relevant skills and their application to medical information and pharmacovigilance work
promote the professions within the pharmaceutical industry and to other professional and trade associations
Obtaining a marketing authorisation for a veterinary medicine can be a costly and time-consuming process and this practical two-day course will equip participants with the key information to achieve a successful application.
Partnerships between pharmaceutical companies are now commonplace for a range of activities. To ensure that all parties meet their obligations, many agreements need to include pharmacovigilance wording, either as part of contracts or more frequently as separate documents.
This module provides advanced training over five days on the principles of drug safety assessment (pharmacovigilance, PV), pharmacoepidemiology (PEp) and pharmacoeconomics (PEc) applied during the development and marketing of medicines.
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