Extreme Transportation Challenges

Life Sciences, Pharmaceutical Regulation, Pharmaceutical, Pharma Manufacturing & Supply Chain,
  • Wednesday, April 23, 2014

Today’s complex world of clinical supply chain requires a proactive risk planning strategy to account for the wide variety of investigational product temperatures and the challenges involved with moving sensitive products across geographies, temperature and time zones.

Euan Douglas from Fisher Clinical Services will provide insights on how to address these challenges, updates on regulatory requirements and examples of new technology that can assist with monitoring and compliance.

Speaker

Euan Douglas, Global Project Director, Fisher Clinical Services

Euan’s career has always been in distribution and logistics, project management and risk analysis. Firstly, with a textile distributor in Bristol, then with American Express and most recently in the Clinical Trial environment with Fisher Clinical Services. Since 2006, Euan has been involved in many key initiatives at Fisher Clinical Services, particularly in the definition, launch and execution of new services related to global Clinical Trials.

A key member of the Strategic Client Relationships Group, Euan has been instrumental in creating the Logistics Knowledge Base which enables clients to maximize efficiencies and reduce costs while minimizing risk across the Clinical Trial Supply Chain. Euan is also a qualified PPI Process Manager and plays a key role in process improvements. He received his BA (Hons) in Business Administration from the University of Brighton.

Message Presenter

Who Should Attend?

Clinical teams, plus professionals in clinical supplies, logistics and outsourcing

Xtalks Partner

Fisher Clinical Services

Fisher Clinical Services is the world’s leading provider of clinical supply chain services.

With a network of cGMP facilities strategically located across the globe to support the conduct of clinical trials, we offer worldwide support for all aspects of clinical supply management including comparator, co-medication and ancillary supply sourcing, packaging, labeling, distribution, storage, through to returns and destruction. With more than twenty years of experience exclusively focused on clinical trials, we can offer guidance and full logistics support across all types of clinical programs and projects.

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