Top Banner
Lynda Paleshnuik | May 2014 1 Copenhagen Workshop May 2014 Session outlines and objectives L. Paleshnuik Lead Quality Assessor PQT
13

Copenhagen Workshop May 2014

Feb 23, 2016

Download

Documents

ophrah

Copenhagen Workshop May 2014. Session outlines and objectives L. Paleshnuik Lead Quality Assessor PQ T. 1. Day 1 • Prequalification: Overview and update • Bioequivalence • WHOPARs and labeling • Quality assessment principles: Part I • API assessment: impurities • Specifications. - PowerPoint PPT Presentation
Welcome message from author
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
Transcript
Page 1: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20141

Copenhagen Workshop May 2014

Session outlines and objectives

L. PaleshnuikLead Quality Assessor

PQT

Page 2: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20142

Schedule of talks

Day 1• Prequalification: Overview and update • Bioequivalence• WHOPARs and labeling • Quality assessment principles: Part I • API assessment: impurities• Specifications

Page 3: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20143

Schedule of talks

Day 2• Packaging• Quality assessment principles: Part II • Pharmaceutical development• Process validation • Stability assessment: API and FPP• Collaborative procedure

Page 4: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20144

Schedule of talks

Day 3• Assessing batch records • GMP issues in quality assessment

Page 5: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20145

Your participation

Days 1 and 2• Open discussion/Q&A on the day’s topics • Participate in the exercises/discussions • Ask questions during/after talks or at the end of the day, • Collect questions for your one-on-one session

Page 6: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20146

Questions

Questions are good• The speaker will say if questions should be held for the end of their talk • Please speak slowly when posing Qs• Questions can be given to any of the facilitators, to be handled at end of day• A speaker may defer a complex question

Page 7: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20147

Your participation

Day 3• Fill out the workshop evaluation(Very important)• One-on-one breakout sessions (feedback and guidance)

Page 8: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20148

Your participation

Day 4• Written exam• Workshop wrap-up and final close

Page 9: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 20149

CTD

Common technical document

Page 10: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 201410

Acronyms!

API – active pharmaceutical ingredientBCS – biopharmaceutics classification systemCOA - certificate of analysisCTD – common technical documentEC – enteric coatedER – extended releaseFDC – fixed dose combinationFPP – finished pharmaceutical productGC – gas chromatography

Page 11: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 201411

Acronyms!

ICH – international conference on harmonizationNMRA – national medicines regulatory authorityPhInt – International PharmacopoeiaPQ/PQT – Prequalification of Medicines TeamPSD – particle size distributionQA – quality assuranceQRM – quality risk managementSPC/SmPC – summary of product characteristics

Page 12: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 201412

Acronyms!

SST - system suitability testingTRS – WHO technical report series publicationWHOPAR – WHO public assessment report

Page 13: Copenhagen Workshop May 2014

Lynda Paleshnuik | May 201456

Questions?

Questions?