Current Issues with the Medicine Supply Chain

Online Training Id: GPP-030

Credits: 6



GBP 410.00

GBP 410.00

This course identifies the changes in Pharmacy Practice standards and introduces the measures necessary to improve Pharmaceutical Practice standards to achieve the Quality ,safety and efficacy necessary for a Patient focused Service in the future

This course will review the potential treats to the Global Medicines Supply Chain and identify the measures necessary to exclude Counterfeit and adulterated medicines and improve delivery performance bay using Block chain technology and Vendor qualification to verify quality  and Enterprise Resource Planning to improve delivery performance of medicines and a clear understanding of the principals of supply chain management.

Credits: 6 CPD / CME

No. of Hours: 6 hrs

Learning Objectives: 

On completion of this course the delegate will have an understanding of

  • Stock shortages and the measures necessary to avoid
  • Measures necessary to exclude of counterfeit and adulterated medicines
  • The application of Block Technology and Track and trace to verify the origin of stock
  • The application of ERP software to carry out the processes of; Product requestioning Planning process - Procurement and Purchasing -Vendor qualification & Quality Management and controlled distribution to wholesalers.
  • The application of LIMS (Logistics Information Management Software) to manage stock in Hospital and Community Pharmacies

Who Should Enroll:

ALL Persons involved in the Practice of Pharmacy which should include – Pharmaceutical Production, Distribution, Wholesale, Hospital and Community Pharmacies who are Dispensing medicines to the patient


Steve Jolley 

Steve Jolley is a subject matter expert in all areas of global safety compliance and signal detection, and is a frequent speaker at leading industry events.

Steve has 35 years’ experience in drug safety & pharmacovigilance and has worked with over 250 clients in North America, Europe, Japan, India, China, the Middle East and Africa. He holds degrees in mathematics and computer science from Cambridge University, England. He is an Adjunct Professor at Rutgers University and teaches part of their Master's degree in Drug Safety and Pharmacovigilance.

Steve is a featured speaker with FDA, EMA and MHRA at conferences and webinars on auditing, signaling and data mining. He is a member of DIA’s training faculty and is an instructor for DIA’s Clinical Safety and Pharmacovigilance Certificate Program. In 2010 Steve was elected as chairman of the DIA’s Clinical Safety and Pharmacovigilance steering committee for North America.

Steve began his career in the pharmaceutical industry in 1985 when he founded DLB Systems, a supplier of computer systems for clinical trials and adverse event reporting to many of the leading life science companies worldwide. DLB was acquired by eResearch Technologies in 1997; since then Steve has worked as an independent consultant.



Online Training Highlights
Duration: 6 hrs
Released On: 06/17/2021
Downloadable Resources: 
Case Studies: 
Need Help?

We can walk you through your program options and Subscriptions please contact us