chevron_left Categories

Other related webinars

Essential Regulatory Perspectives and Best Clini...

Monday, 7th February, 2011
Time : 01:00 PM EST | 10:00 AM PST

Biggest challenge for Pharmaceuticals/ Biotechno...

Tuesday, 22nd February, 2011
Time : 10:00 AM | 07:00 AM

Critical aspects of applying QbD to pharmaceutic...

Friday, 6th May, 2011
Time : 02:00 PM | 11:00 AM

Biologics Battlefield: Opportunities and Obstacl...

Thursday, 30th June, 2011
Time : 02:00 PM | 11:00 AM

Vital Success/Failure Regulatory Perspectives an...

Thursday, 15th September, 2011
Time : 02:00 PM | 11:00 AM

Good Laboratory Practices (GLP) Compliance and A...

Friday, 11th November, 2011
Time : 02:00 PM | 11:00 AM

Good Clinical Practice (GCP): FDA Regulations, S...

Thursday, 26th January, 2012
Time : 02:00 PM EST | 11:00 AM PST

Orphan Drugs in Europe – How to use observatio...

Friday, 1st June, 2012
Time : 02:00 PM EST | 11:00 AM PST

Implementing the Compliant Good Laboratory Pract...

Friday, 10th August, 2012
Time : 02:00 PM EST | 11:00 AM PST

An overview of an innovative patient-centric ser...

Wednesday, 12th September, 2012
Time : 02:00 PM EST | 11:00 AM PST

An overview of Translational Medicine

Friday, 21st September, 2012
Time : 02:00 PM EST | 11:00 AM PST

Optimizing Site Selection for Global Clinical Tr...

Friday, 26th October, 2012
Time : 02:00 PM EST | 11:00 AM PST

Optimal clinical supply planning for global drug...

Friday, 16th November, 2012
Time : 02:00 PM EST | 11:00 AM PST

Patient Recruitment & Retention Management in Cl...

Monday, 10th December, 2012
Time : 02:00 PM EST | 11:00 AM PST

GMP's for Dietary Supplements: Keys to Success w...

Thursday, 30th October, 2014
Time : 01:00 PM EST | 10:00 AM PST

Is It Safe? A Cautionary Tale and Practical Guid...

Friday, 9th January, 2015
Time : 02:00 PM EST | 11:00 AM PST

How To Reconcile ICH GCP With RISK BASED Monitor...

Thursday, 19th March, 2015
Time : 11:00 AM IST | 06:30 PM BET

Orphan Drugs : Regulation and Reimbursement Cond...

Friday, 22nd July, 2016
Time : 01:00 PM EST | 10:00 AM PST

Panel Discussion on Best Practices to Clinical T...

Friday, 10th March, 2017
Time : 04:00 PM IST | 11:30 AM BST

FDA Requirements for Good Clinical Practice’s ...

Friday, 7th July, 2017
Time : 04:00 PM IST | 11:30 AM BST

Implementation of Pharmaceutical Quality system ...

Friday, 17th November, 2017
Time : 01:00 PM EST | 10:30 AM PST

FDA Guidance for ICH GCP E6 R2 Means for Sponsor...

Thursday, 27th September, 2018
Time : 04:00 PM IST | 03:30 AM PDT

Managing Human Error in Quality Systems: Human E...

Friday, 17th July, 2020
Time : 01:00 PM EST | 10:00AM PST

FDA approvals of Orphan Drugs and Rare Diseases:...

Friday, 24th July, 2020
Time : 01:00 PM EST | 10:30 AM PST

FDA approvals of Orphan Drugs and Rare Diseases:...

Friday, 26th August, 2022
Time : 01:00 PM EST | 10:00 AM PST

Good Documentation Guideline (Chapter <1029> USP...

Friday, 11th November, 2022
Time : 01:00 PM EDT | 10:00 AM PST

FDA - Investigating OOS results

Friday, 17th March, 2023
Time : 01:00 PM EDT | 10:00 AM PDT

Best Practices for FDA's Investigating Deviation...

Friday, 26th May, 2023
Time : 01:00 PM EDT | 10:00 AM PDT

Recorded Webinar

Optimal clinical supply planning for global drug development

timelapse 60 mins with 10-15 mins of Q and A

Note:

This webinar occured in the past
Along with recorded webinar, copy of presentation slides will be shared
Recorded Webinar can be played unlimited times

Speaker/Presenter

Short Abstract

Clinical Trial Materials (CTM) and comparators are often expensive and sometimes scarce items on the critical path to completing a clinical trial. Multiple investigator sites (often in different countries), each with variable startup schedules and uncertain patient accrual rates make planning and management of inventory positions difficult and shipping costs significant. Therefore, major issue in clinical supply planning is cost optimization, and at the same time :

This presentation will cover the following areas :

  • Alignment of manufacturing production schedule and sites demand.
  • Management of inventory levels
  • Mitigation of stock-out risk and optimization of overages
  • Optimization of shipment schedule & package size


Comprehensive solution is based on combined usage of powerful mathematical tools including optimization tool (cost minimization, optimal delivery schedule and package size), simulation tool (stock-out risk assessment and analysis of risk mitigation strategies), predictive patient recruitment models, and others. Case study will illustrate proposed approach.


Apply for this webinar

Who should attend

CEOs, VPs, Directors, Heads, Managers working within:

  • Clinical Affairs
  • Compliance Specialists and Officers
  • Clinical Trials
  • Quality Professionals
  • Drug Development
  • Consultants, Contractors/Subcontractors
  • Anyone Interested in Learning More About Clinical Trial Materials

Content Disclaimer

Contents in our website are from external websites. Links to and content from external website are provided for the convenience of users. Biopractice.com takes no responsibility for the content of such links and websites.

//