Your event should be here ! To publish, manage, promote... To learn or to be formed ... Online registrations

Site language : English - Français
Ref : 32752
Event :PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

Dates :Thursday March 18th, 2021 - Friday March 19th, 2021

Location :Virtual Seminar
6201 America Center Drive
Suite 240
95002 San Jose, United States

Type :Conference & Seminar - International audience

Accreditation :--


 

Further information

Editorial

In this two day workshop conference we will review the EMA and FDA requirements regarding Risk Based Audits of the PV system and Quality System. The course will focus on the design of the PV audit strategy, identification of the PV processes and entities subject to PV audit (define the PV audit universe), development of risk assessment methodology, development of procedures/tools to monitor PV processes and activities, and implementation of the PV audit strategy plan. Additionally, we will review methods of quality oversight and management of third parties performing PV activities.
 

Objectives

  • Understand the legal requirements and health authority expectations for a risk based audit program and current interpretation. Plan, develop and implement the PV Audit Strategy Plan, which includes the following processes:
    • Develop a high-level PV audit strategy
    • Identify the PV activities and processes subject to PV audit
    • Develop risk assessment criteria
    • Identify the PV audit universe – entities subject to PV audit
    • Categorize the entities subject to PV audit
    • Perform risk assessments
    • Prioritize entities for audit according to relative risk
    • Prepare a 3-5 year PV audit plan
  • Identify procedures/tools to monitor PV quality of third parties


 

Program

Day 01(9:00 AM - 5:00 PM EDT)
  • 09.00 AM: Session Start
  • Review of FDA and EMEA requirements for risk based PV audits
  • The pharmacovigilance system and the quality system
  • Strategic level audit planning
  • Hands on exercise
  • PV activities and processes subject to PV audit
  • Risk assessment criteria
  • The PV audit universe - all entities subject to PV audit
  • Safety data exchange agreements (SDEAs) and vendor contracts
Day 02(9:00 AM - 5:00 PM EDT)
  • Stability (shelf-life) studies
  • Categorization of the entities (PV Audit Universe)
  • Risk assessments
  • Prioritization of entities for audit according to relative risk
  • 3-5 year PV audit plan
  • Hands on exercise
  • Procedural documents, e.g. SOPs
  • Identify procedures/tools to monitor PV quality for oversight of third parties
  • Q & A

Speakers

Cynthia is an accomplished executive director and chief compliance officer with over 17 years’ experience providing first-to-market solutions to the challenges sponsor face whilst using risk management strategies to mitigate ones in the future. She is an industry expert with contributions to over 450 sponsor programs with proven track record of optimization, quality, compliance, and fiscal responsibility. Cynthia is a certified Quality Assurance (QA) and Regulatory Affairs (RA) executive, principal consultant and published biotechnologist with an emphasis in fabricating quality-based process and product development strategies in regulated pharmaceutical, medical device and biopharma industries. In her tenure she has lead strategic partnerships to solve the complexities of the life science industry by providing tailored expertise with the time and resources necessary to mitigate the challenges sponsors face with expertly sourced solutions. She drives QBD initiatives into corporate portfolios to which traverse all phases of development and deployment from a financial, operative, quality, and regulatory vantage. As an expert in national and international GxP regulations, standards and guidance's, her expertise has been engaged as an international HA consultant for over 7yrs with support that traverses all product development phases to deploy best in class programs for industry sponsors including, but not limited to, Gilead, Daichi-Sankyo, Bristol Myers Squib, Amgen, Abbott, Novartis, and Roche.


 

Organizing committee

Complianceonline

Location

Map and directions
Conference address :
Virtual Seminar
6201 America Center Drive
Suite 240
95002 San Jose
United States
tel : +1-888-717-2436
Map and directions

Further information

To access the information you need to be connected. Creating an account is easy and free!

Log to your account
Register on Doctorama

Details

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation Pharmacy
pharmacovigilance audit strategy planning, good pharmacovigilance practices, pv audit strategy plan, risk based pharmacovigilance audits, pharmacovigilance audit plan, fda pharmacovigilance audits, pharmacovigilance audit checklist, pharmacovigilance auditing training
Professionals
-- -- --
--

Other

For more information on PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation, plsase contactr ComplianceOnline

To display announcer website, obtain a letter of invitation, you must be logged

Log to my account
Register on Doctorama


Recommend this event