Maximize Your Professional Development at These Signature Events
Registration is now open for ISPE's Process Validation and Process Validation Statistics Conferences! Join us 12 – 15 September in Bethesda, Maryland to take advantage of these exceptional technical forums for those knowledgeable in process validation and statistics. Discover why:
90% of the attendees would recommend these conferences to their colleagues
Attendees rated the sessions/presentations Good or Excellent on their quality and relevance
19 international attendees from 13 different countries, other than the US, attended these conferences in 2016
ISPE 2017 Process Validation ConferenceOutcomes that Matter: Benefits of Implementing the Process Validation Lifecycle 12 – 14 September 2017 Explore each of the three stages in the validation lifecycle, and delve into areas that present significant challenges and opportunities.
Implementation of continuous process verification and qualification
Industry standard practice on confidence and reliability level Small molecule API validation's relation to drug product
Small molecule API validation's relation to drug product
ISPE 2017 Process Validation Statistics Conference Leveraging Statistics in the Process Validation Lifecycle 13 – 15 September 2017 Gain insights and practical approaches to meet the increasing expectations for the use of statistics across the product lifecycle.
Interpret and implement statistical elements of regulatory guidance
Leveraging risk assessment and risk management in the PV lifecycle
QbD approach in analytical method development and validation
Register by 1 August to save $200 or more. To learn more and save while doing it, register for both these signature conferences and receive an additional 25% discount!
The ISPE GAMP® Guide: Records and Data Integrity provides you with principles and practical guidance on meeting current expectations for the management of GxP regulated records and data—ensuring that they are complete, consistent, secure, accurate, and...
"Pharma needs to ensure it pays attention to how patients feel about the way they are taking their medication. By listening to patients, pharma can help simplify adherence for the patient."
This is just one of the messages Christine Milligan, as Team...
Phillip Lyman and David Burgos of CRB Consulting Engineers, Inc., presented a case for implementing a process simulation approach in the session, “Improving Package Line Efficiency with Simulation.” Assumptions, input data and a typical model...