GDP - Time & Temperature Controlled Logistics l Clinical Trial Supplies Logistics Conference • 22 & 23 November 2017 • Frankfurt

 

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International Pharmaceutical/Biopharmaceutical

GDP Pharma Logistics I Clinical Trial Supplies Logistics

Symposium

 

Logidays 2017

Stream A

Stream B

 

Pharmaceutical Logistics is focused on addressing key challenges associated with commercial logistics and medicinal products shipped globally. The emphasis is optimization of the logistics process, obstacles within supply chain, importance of thermal mapping for storage and storage during transport. The overall program varies, with topics concerning educational needs to clearly understand the role of technologies such as thermal covers, data loggers and thermal packaging, but also best practices in deciding which logistic provider is most appropriate for you. While an underlying theme is focused on Good Distribution Practice in practice and best approach for Audit Preparation subject to Quality Assurance needs and the role of Qualified Person.

 

Key Regulatory and standards covered: Good Distribution Practice, FDA, Latest in Pharmaceutical Air, Land and Ocean Logistics requirements, Technical Reports for Thermal Packaging, World Health Organization among others. 

Clinical Trial Supplies Logistics is engaging an in-depth coverage of sourcing, comparator, production, storage and transportation of Investigative Medicinal Products (IMPs) and Non-Investigative Medicinal Products (NIMPs). Clinical Trial Supplies is subjugated to in-depth scrutiny where the fundamentals of decision making is shared based experience and open-unobstructed dialogue. With aid from key note industry experts thought leadership is provided as means of direct involvement in a CTS conference where you are challenged to think differently.

 

 

 

 

Key Regulatory and standards covered: Good Clinical Practices, Good Manufacturing Practice, Good Laboratory Practice, Good Distribution Practiced, European Clinical Directive and Global Standard 1 among other key standards

 

ENGAGE YOUR PEERS

 

GENEROUS BOOTH SIZE

 

LEARN FROM INDUSTRY'S LEADERS

 

SHOWCASE YOUR SERVICES

 

DEMONSTRATE YOUR CAPABILITIES

 

CREATE LONG-LASTING PARTNERSHIPS

 

 INTERACTIVE WORKSHOPS

 

DISPLAY YOUR PRODUCTS

Value of Attending

 

  • Knowledge Transfer: Two complete days dedicated to your Priorities, networking with your peers and take advantage of the opportunity to learn, share knowledge and experience, create contacts and evaluate how new technologies can better impact your work.
  • Real-World Information: Expand your knowledge and experience by being in contact with contacts from the leading pharma - biopharma companies in globally. Share knowledge within your organisation and receive current real-time updates.
  • Training: You are educated based on sharing of experience and assist your business activities with practical benchmarking. Case studies, presentations, open panel discussions and experiences shared.
  • Learning: Engage key techniques in better interpretation of key standards and regulatory requirements from the Actual Regulators who issue the compliance requirements.
  • Detailed Delegate Pack: Receive all presentations & audio of the speaker presentations, along with all educational material of the conference so that you can share the knowledge with your team and organisation.

Business Dialogue Events

Testimonials

 

Webinar Examples

Jan Walbrecker, Senior Software Developer

 

 

 

Using the Virtual Cold Chain for Cost-Effective Lane Risk Analysis

Riekert Bruinink, Senior GMP/GDP Inspector, Dutch Health Care Inspectorate, The Netherlands - Member of the GDP drafting Group of the European Medicines Agency

 

GDP Audits: Weak points when conducting GDP AUDIT based on inspections

Eugenio Filippi, Senior Manager Plasma Logistics Europe, Shire

 

 

 

3PL End-to-End Process Excellence to Ensure Uninterrupted Delivery

Florian Siedenburg, CEO, Ecocool

 

 

 

Handling Tarmac Times - Easymade!