Case study: creating a blueprint for pharmaceutical distribution - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Case study: creating a blueprint for pharmaceutical distribution





Prior to the appointment of NYK, AZ's manufacturing plants had operated independently and been responsible for managing their own transportation. As such, the union with NYK represented a radical departure from the pharma company's previous transportation model. The project also encouraged AZ's supply chain to move from a push system to a pull system through the introduction of lean manufacturing and supply chain principles.

Key objectives for NYK

  • Secure competitive pricing rates.
  • Establish common quality and security standards across Europe.
  • Exploit opportunities to co-load product from multiple AZ plants.
  • Exploit opportunities to co-load product with other pharmaceutical manufacturers within NYK's established panEuropean pharmaceutical network.
  • Develop long-term cost reduction and continuous improvement culture.
  • Achieve environmental benefits as a result of decreased air and road transport.

Implementation

Not underestimating the challenges of implementing such a major change, the companies worked closely together to ensure a seamless transition to the new systems. Product integrity was the first priority. The early development of service level agreements and standard operating procedures both between AZ and NYK, and, perhaps more importantly, NYK and its subcontractors, ensured that quality was builtin from the beginning.

To minimize risk elements, a phased implementation plan was produced to allow sites to:

  • Be managed on an individual basis.
  • Have training and operational issues addressed.
  • Have hauliers audited.
  • Have common standards achieved.
  • Have processes designed and tested.

Environmental considerations

Until recently, quality and load integrity were the principal considerations when selecting logistics partners and, because of this, major pharmaceutical customers tended to demand dedicated vehicle solutions, which can create attendant inefficiencies. Whilst quality and integrity remain primary considerations, two further issues are also gaining importance: cost and the environment. As a consequence, pharmaceutical manufacturers are showing increasing willingness to share resources to improve asset utilization (particularly through better vehicle fill) and to reduce costs.

Co-loading

NYK operates a central 'control tower' that provides a 'helicopter' view across Europe, allowing centralized planning of the panEuropean transportation operation to maximize vehicle utilization, reduce costs and deliver environmental benefits. Through its network of European subcontractors and partners, NYK was able to provide AZ with a robust, consistent pan-European transport network with a single point of contact and also provided opportunities for AZ to consolidate volumes with volumes from other pharmaceutical manufacturing customers. Whilst shared-user networks are well established and widely used in other sectors, the sharing of vehicles by pharmaceutical manufacturers is unprecedented.

Plans from AZ's sites are received a week in advance, which enables NYK's planning team to identify load consolidations, triangular routes and roundtrip opportunities across all sites. NYK then contacts the sites to discuss potential changes that will enable maximum load consolidation and produces agreed plans, which are circulated to all sites.


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
What is the single greatest threat to maintaining manufacturing processes at your facility?
Quality issues
Facility/environment problems
Process development problems
Production equipment downtime
Raw material supply problems
Regulatory restrictions
Business decisions to limit production
Quality issues
67%
Facility/environment problems
0%
Process development problems
0%
Production equipment downtime
0%
Raw material supply problems
33%
Regulatory restrictions
0%
Business decisions to limit production
0%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Patent Settlements Become More Risky
Praise and Perils for Biotechnology Patent Policy
Risk-Mitigation Strategies in Drug Manufacturing for Emerging Markets
Quality Focus: Ensuring Raw Material Transparency
Advertising of Prescription Drugs  Keeping it Honest and Balanced

Click here