Clinical Trial Supply Europe 2023

2023 will see the return of the Clinical Trial Supply Europe conference to Milan where pharma, large and small, alongside biotechs will have the opportunity to discuss, debate and consider new technologies and processes to streamline supply chain operations.

15 - 16

March

2023
  • NH Milano Congress Centre, Italy
  • Complimentary
  • Why attend?
  • Agenda
  • Speakers
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  • Sponsors
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Why attend?

WHAT TO EXPECT FOR 2023?

Clinical Trial Supply Europe is the meeting place for the pharmaceutical and biotechnology community to discover how to excel in clinical supply strategy as well as form key connections for long-term success.

350+

Attendees

55+

Exhibitors

20+

Speakers

85%

Attendees at Director+ level

350+

Attendees

55+

Exhibitors

20+

Speakers

85%

Attendees at Director+ level

See What It's All About

Agenda

  • 15 Mar 2023
  • 16 Mar 2023
Expand All

Streams

Stream one

Clinical Supply Logistics and Operations

Stream two

Clinical Supply Technology and Innovation

11:15 AM

PANEL DISCUSSION: Uncovering new trends and technological advancements for the European clinical supply chain: what’s new for 2023?

  • Considerations for clinical supply chains in Europe for 2023: how have Brexit, the Russia-Ukraine conflict, and other factors impacted trial supply?
  • An overview of emerging technologies and processes to support clinical supply chains in Europe
  • How the Clinical Trial Regulation and other regulatory factors are impacting European clinical supply chains
  • Opportunities created by data-driven technologies such as AI and machine learning for clinical supply chains
  • Linking everything back to the patient: how new clinical supply technology will benefit patients in clinical trials

Speakers

11:45 AM

Reserved for N-Side

12:15 PM

CASE STUDY: Designing a direct-to-patient distribution model for your clinical supply chain

  • Benefits to patients of direct-to-patient models: how can DTP make clinical trials more accessible?
  • Implementing a DTP strategy that works for your clinical study
  • Understanding how DTP can optimise supply chain flexibility for clinical trials

Speakers

12:45 PM

Reserved for Medidata

1:15 PM

Lunch and networking

2:30 PM

PANEL DISCUSSION: Making a success of direct-to-patient for your clinical trials

  • Considerations when designing a DTP strategy
  • Navigating regulatory frameworks, both in Europe and beyond
  • Identifying vendors and partners in order to deliver DTP successfully
  • Understanding the benefits of DTP from a patient perspective and the importance of this
  • Overcoming common pitfalls and hurdles in DTP

Speakers

3 PM

Reserved for 4G Clinical

3:30 PM

How clinical trial supply managers can reduce the patient burden from a fear reduction perspective

  • Understanding where patient concerns lie when participating in clinical trials and what pharma companies can do to mitigate against these
  • Aiming to reduce the burden of trial participation on patients as much as possible: where are pharma companies falling short?
  • What more needs to be done when it comes to patient accessibility for clinical trials?
  • The benefits of systems like direct-to-patient for increasing patient accessibility for clinical trials

Speakers

4:30 PM

Incorporating technology to increase clinical supply chain efficiency

  • Assessing emerging technologies: what is available for improving supply chain efficiency?
  • How effective use of data and data management tools can help streamline your supply chain
  • Training staff and logistics partners on up to date technology: overcoming hurdles surrounding this

Speakers

5 PM

Reserved for IQVIA

Speakers

7:30 AM

Registration and refreshments

8:20 AM

Chairperson’s opening remarks

Speakers

8:30 AM

Transforming our supply chain by investing in key capabilities: processes, people and digital

  • Developing a new strategy to build a leading supply organisation capable of dealing with an ever increasing and complex portfolio
  • How a digital transformation will enable significant business value in terms of increasing efficiency and driving down waste

Speakers

9 AM

Reserved for Suvoda

9:30 AM

Innovating your clinical trial supply chain: what to think about in 2023

  • Re-assessing your thinking: understanding how clinical trials can be a source of value and development
  • Identifying the opportunities to innovate across your clinical trial supply lifecycle
  • Clinical supply as a critical link in clinical trials: how to work collaboratively and effectively with clinical operations teams

Speakers

10 AM

Reserved for Edo Madussi

Speakers

10:30 AM

Morning refreshments and networking

11:15 AM

Forecasting and demand planning in the supply chain: preparing for uncertainty

  • Ensuring flexibility in your budget supply strategy to cater for unexpected situations
  • Demand planning when there is uncertainty around patient enrolment: the importance of communicating with your clinical operations team
  • Learnings from the COVID-19 pandemic and the Russia-Ukraine conflict in terms of managing clinical supply in times of uncertainty

Speakers

11:45 AM

Reserved for Berlinger

12:15 PM

Getting your pharmaceutical products seamlessly into the US: what you need to know

  • Breaking down all that you need to know about CBP and other agency importation requirements to facilitate clinical supply shipments
  • Receive detailed information on how to correctly declare biological products at the US border (Ports of Entry)
  • Discover which biological products may have transportation restrictions that must be factored into your clinical supply chain strategy
  • Review case examples of non-compliant shipments

Speakers

12:45 PM

Reserved for Almac

Speakers

1:15 PM

Lunch and networking

2:30 PM

Effective strategies for sourcing comparators and placebos

  • Accessing supply: ensuring your supply chain is robust and planning timelines to avoid delays
  • Managing regulatory hurdles when importing comparators from overseas
  • What to consider in order to ensure your comparator sourcing processes meet cost and waste targets

Speakers

3 PM

Holistic approach to effective clinical trial supply strategies: beyond comparator sourcing

  • Biosimilar and generic product benefits and regulatory framework
  • Competitive advantage: Bolar exemption in practice
  • Why science and not wholesale mindset should drive your approach

Speakers

3:30 PM

PANEL DISCUSSION: Running your clinical trial internationally: overcoming logistical challenges to maximise supply chain efficiency

  • Regulatory considerations when shipping across borders, both within Europe and cross-continent
  • Shipping biologics cross-border: what you need to know, and how to prepare in advance for this
  • How geopolitical factors have influenced clinical supply chains in Europe and how to mitigate the impact of this
  • Assessing the benefits of air, sea, road and rail as methods of transporting drugs around Europe

Speakers

4 PM

Afternoon refreshments and networking

4:30 PM

Supply chain efficiency and data driven performance

  • Using technology to improve your systems while remaining cost-effective
  • Best practice in ensuring your supply chain is as efficient as possible
  • Measuring supply chain KPIs and identifying areas of weakness

Speakers

5 PM

Reserved for Abacus Medicine

5:30 PM

IMP during the Ukrainian conflict: an inspiring story of humanity

  • A case study of how Galapagos kept their clinical supplies running in Ukraine this year
  • Crisis management: key takeaways in keeping supply chains running smoothly during times of crisis
  • Learnings from disruption to European supply chains as a fallout of the Russia-Ukraine conflict

Speakers

6 PM

Chairperson’s closing remarks

Speakers

Streams

Stream one

Clinical Supply Logistics and Operations

Stream two

Clinical Supply Technology and Innovation

9 AM

PANEL DISCUSSION: Automation in clinical supply chains: what level of automation can you incorporate?

  • Analysing cost vs benefit of automation in supply chains: at what point does automation become cost effective?
  • Understanding risks associated with automating supply chains
  • How IRT and simulation system capabilities can help manage supply chains automatically

Speakers

9:30 AM

Reserved for Calyx

10 AM

FIRESIDE CHAT: The clinical to commercial transition in packaging: managing and aligning different prime directives

  • Choosing packaging options when taking your drug from a clinical trial to market: an overview of key considerations to take into account
  • Should we be designing packing for trial drugs with commercialisation in mind?
  • Communicating effectively with your commercial department: how to ensure design of the best possible commercial packaging

Speakers

10:30 AM

Reserved for Parexel

11 AM

Morning refreshments and networking

8 AM

Registration and Refreshments

8:50 AM

Chairperson’s opening remarks

Speakers

9 AM

Choosing a manufacturing partner: what to consider when selecting a CMO

  • Preparing for a clinical trial: choosing the right CMO to manufacture your product
  • Balancing cost with quality when selecting a CMO
  • Understanding increasing complexity in clinical setup with different CMOs and shared sponsoring
  • Ensuring the best setup to work constructively with your CMO
  • Handling expectations and getting the relationship right

Speakers

9:30 AM

Reserved for Biocair

Speakers

10 AM

Harnessing the benefits of e-labelling: accelerating packaging and labelling processes through technological innovation

  • E-labelling as a patient friendly solution
  • Emphasizing the value of e-labelling for your supply chain planning: overcoming the expiration date hurdle
  • Navigating the risks and the rewards; considering costs, timelines, contingency plans and patient safety
  • Understanding the drive behind the development of e-label technology: success stories vs lessons learned

Speakers

10:30 AM

Reserved for TSS

11 AM

Morning refreshments and networking

11:30 AM

PANEL DISCUSSION: Operational agility: the importance of maintaining flexibility in your clinical supply chain

  • With trials more and more complex, how do you ensure supply chain operations are agile and flexible?
  • What can we do to be as flexible as possible to handle changes in demand, particularly when shipping internationally?
  • Ensuring you are prepared for a crisis: what the pandemic has taught us about being prepared for every eventuality

Speakers

12 PM

Reserved for DHL

12:30 PM

Vendor management: the importance of aligning vendors and sponsors under one shared goal to deliver your trial

  • Handling vendors when working remotely: tips for fostering a strong relationship virtually
  • How much oversight do you need to have over your vendors and partners, and how involved should you be in the process?
  • Overcoming challenges involved when working with multiple vendors in order to ensure everyone’s goals are in line

Speakers

1 PM

CASE STUDY: Incorporating e-labelling into your clinical trial supply processes

  • Navigating regulatory hurdles around e-labelling, in particular the new Clinical Trial Regulation
  • How e-labelling can improve the patient experience and thus engagement and retention in trials
  • Using e-labels as a way to increase efficiency and reduce costs: where are the main benefits and opportunities?

Speakers

1:30 PM

Lunch and networking

2:30 PM

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

During the roundtable discussion session, the conference hall will be divided into two ‘zones’. Delegates can choose which zone they would like to join. Each zone will be led by a table moderator and will focus on a different challenge within clinical trial supply. After 45 minutes, delegates will have the opportunity to swap and choose a different table, and each roundtable will run twice.

 

ROUNDTABLE 1: Selecting vendors and partners for your supply chain: key considerations

Ilaria Rondinone, Clinical Trial Supply Co-ordinator, Chiesi Group

 

ROUNDTABLE 2: Usage of internal systems for outsourced manufacturing steps

Chiranth Hulgur, Senior Manager Clinical Supply Chain Data and Analytics, CSL Behring

 

ROUNDTABLE 3: Forecasting the unexpected: how to handle unforeseen circumstances to reduce impact to clinical supply chains

Ruth Barbero, Associate Director Global Clinical Supply Chain, Incyte

 

ROUNDTABLE 4: The pros and cons of just in time labelling: what to consider when adopting this as a strategy

Dr Kamal Amin, Head of Clinical Supplies Management, Galderma

 

ROUNDTABLE 5: End2End visibility in clinical trial supply

Ulrich Mengel, Associate Director, CTS Business Operations, CSL Behring

Speakers

4 PM

Chairperson’s closing remarks

Speakers

Speakers

Select a speaker to learn more

Back
Edo Madussi
Managing Director, Euromed Pharma

Edo Madussi is the Managing Director, of Euromed Pharma US and Business Unit head of the Clinical Trial Division at the Petrone Group.

His business experience combined with his academic background and four spoken languages - English, German, French, and Italian - brought him to develop an extensive network within the global clinical supply chain space.  He is currently developing one of the latest ventures of the Petrone Group: a US-based integrated platform to support Clinical Trial Sponsors and other industry players around the world with a wide range of services in the R&D space.

Session Details:

Reserved for Edo Madussi

2023-03-15, 10:00 AM

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Ruth Barbero
Associate Director Global Clinical Supply Chain, Incyte

BSc in Pharmacy, MSc in Pharmaceutical Industry and Technology, MSc in Pharmaceutical Biotechnology. Currently studying an Executive MBA. After exploring opportunities in the academia and as community pharmacist I developed my career in the pharmaceutical industry were I have been working for about 12 years, initially in formulation and manufacturing within pharmaceutical development, and during the last 7 years in Clinical Supplies. I have worked for Almirall and AstraZeneca in Spain and for Galderma, Debiopharm and Incyte in Switzerland. I have recently moved back to Spain were I am still working for Incyte within the Global Clinical Supplies group.

Session Details:

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

2023-03-16, 2:30 PM

Session Details:

Forecasting and demand planning in the supply chain: preparing for uncertainty

2023-03-15, 11:15 AM

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Amaury Jeandrain
Senior Director, Solutions Engineering and Partnerships, N-Side

Amaury Jeandrain has a Master’s Degree in Business Engineering with a specialization in supply chain management. After working for a CRO, he joined N-SIDE where he supported the optimization of hundreds of trials from different indications and pharmaceutical companies, providing services ranging from risk-based optimization to clinical trial design and solving drug supply shortage problems. Amaury now leads a group of consultants, focusing on the extension of N-SIDE’s solutions.

Session Details:

PANEL DISCUSSION: Uncovering new trends and technological advancements for the European clinical supply chain: what’s new for 2023?

2023-03-15, 11:15 AM

Session Details:

FIRESIDE CHAT: The clinical to commercial transition in packaging: managing and aligning different prime directives

2023-03-16, 10:00 AM

Session Details:

PANEL DISCUSSION: Automation in clinical supply chains: what level of automation can you incorporate?

2023-03-16, 9:00 AM

Session Details:

PANEL DISCUSSION: Making a success of direct-to-patient for your clinical trials

2023-03-15, 2:30 PM

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Vanessa Dekou
Managing Director, CSI

Vanessa is the MD of Clinical Services International (CSI) a leading provider of Clinical Trial Supplies to the Biopharmaceutical Industry. Vanessa started her career as a research associate at Scotland Yard. Subsequently she worked for leading CROs and with some of the largest biopharmaceutical and Biotechscompanies to provide innovative solutions. She has extensive experience in drug development from Preclinical to registration and commercialization strategies and has secured product registration for several orphans and first in class drugs. She has a PhD in Cardiovascular Genetics from UCL, an MBA from Cambridge and Masters in Market Access from University m University of Lyon.

Session Details:

Chairperson’s opening remarks

2023-03-15, 8:20 AM

Session Details:

Chairperson’s closing remarks

2023-03-15, 6:00 PM

Session Details:

Holistic approach to effective clinical trial supply strategies: beyond comparator sourcing

2023-03-15, 3:00 PM

Session Details:

PANEL DISCUSSION: Running your clinical trial internationally: overcoming logistical challenges to maximise supply chain efficiency

2023-03-15, 3:30 PM

Session Details:

Chairperson’s closing remarks

2023-03-16, 4:00 PM

Session Details:

Chairperson’s opening remarks

2023-03-16, 8:50 AM

Session Details:

PANEL DISCUSSION: Operational agility: the importance of maintaining flexibility in your clinical supply chain

2023-03-16, 11:30 AM

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Arnaud Dourlens
Head of Clinical Trial Supply, Sanofi

Arnaud Dourlens is an Arts et Métiers engineer, he began his industrial career in the FMCG sector where he held growing responsibilities. Then he joined the LVMH group where he reorganized new product launches and industrial investments in the Make-up segment in order to adapt to the need for innovation and time to market, thus providing a competitive advantage. He then managed the entire portfolio of industrial launches and investments in Perfumes, Skincare and Make-up for Parfums Christian Dior Group.

During his career Arnaud held a wide variety of industrial roles. He joined Sanofi in 2017 as Production Director of a major solid oral form production site (>2.5 billion € turnover). He has been a key player in the development of the continuous improvement mindset and in the transformation of the site through IT projects, investments and activity growth following the acquisition of Boehringer Ingelheim consumer healthcare portfolio.

Since the beginning of 2020, he’s been the global head of Sanofi Clinical Supply Chain Operations, managing worldwide clinical supply teams involved in more than 300 clinical studies.

Session Details:

Innovating your clinical trial supply chain: what to think about in 2023

2023-03-15, 9:30 AM

Session Details:

PANEL DISCUSSION: Uncovering new trends and technological advancements for the European clinical supply chain: what’s new for 2023?

2023-03-15, 11:15 AM

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Sean Smith
Biological Threat Exclusion Coordinator, US Customs And Border Protection

Sean Smith is a Biological Threat Exclusion Coordinator (BTEC) for CBP in the Office of Field Operations/ Agriculture Programs and Trade Liaison/ Agro/Bio-Terrorism Countermeasures. As a BTEC, Mr. Smith is charged with supporting and developing U.S. Customs and Border Protection (CBP) operational capacity and capability in preventing tools of agro/bio-terrorism from entering the U.S.

Mr. Smith joined CBP in 2005 as an Agriculture Specialist (CBPAS) and was promoted to Supervisory CBPAS in 2008. He has served CBP in the following ports of entry: San Diego, San Ysidro, Otay Mesa and Boston Logan Airport. From 2011- 2018, Mr. Smith served as the primary Public Affairs Liaison and Border Community Liaison, respectively, for CBP in New England. He has also volunteered to assist in past domestic and international CBP disaster recovery operations, including: Hurricane Ike (2008), 'Operation Safe Return' (Haitian Relief Effort- 2010), and Hurricane Harvey, DHS Surge Capacity Force (2017).

Prior to CBP, Mr. Smith contributed to wildlife conservation for nearly a decade, completing field work on rare endemic Hawaiian birds on the Big Island of Hawaii, and raising rare and endangered birds (in some cases, extinct in the wild) at the San Diego Zoo's Avian Propagation Center. Also, Mr. Smith is a former reserve firefighter and EMT for the City of Borrego Springs in California. He holds a Bachelor of Science degree in Ecology and Systematic Biology from Cal Poly San Luis Obispo, California.

Mr. Smith, his wife, two children, one dog, and one chicken live in an old farmhouse in Massachusetts.

Session Details:

Getting your pharmaceutical products seamlessly into the US: what you need to know

2023-03-15, 12:15 PM

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Révérien Uwacu
Clinical Trial Supply Manager, UCB

Session Details:

CASE STUDY: Designing a direct-to-patient distribution model for your clinical supply chain

2023-03-15, 12:15 PM

Session Details:

PANEL DISCUSSION: Making a success of direct-to-patient for your clinical trials

2023-03-15, 2:30 PM

Session Details:

CASE STUDY: Designing a direct-to-patient distribution model for your clinical supply chain

2023-03-15, 12:15 PM

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Thomas Thoma
Head Managed Access Programs, CTS/GHT/SR, Teva Pharmaceuticals

Three University degrees at the University of Augsburg 5 years of Supply Chain Management responsibilities in automotive electronics industry 12 years of Management responsibilities in multiple roles (SCM, IT, Sales) in the pharma industry Since 2014 Head of Clinical Trial Supply (Sales) of Teva Europe. Offering Teva widest pipeline of pharmaceuticals, placebos and manufacturing for clinical trial purposes. Since 2017 Head of Global Health Tendering of Teva Global. Offering Teva widest pipeline to NGOs, GOs and UN related organizations. Married and father of three beautiful kids

Session Details:

FIRESIDE CHAT: The clinical to commercial transition in packaging: managing and aligning different prime directives

2023-03-16, 10:00 AM

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Roel van der Heijde
Facilitator & Trainer, Rotterdam And Patient Experience Association

Roels inspiration: “Be the change you wish to see in the world” - Ghandi Roel van der Heijde lives in Rotterdam, The Netherlands. He has a MA in International Business, is an international acknowledged NLP trainer, executive team coach and a certified death and grief counsellor. He is a driven and experienced trainer and facilitator in: - Patient Fear Reduction (for all caregivers); - Team Collaboration; - Vulnerability & Leadership; - Discrimination & Inclusion. Roels motivation: “Acknowledgement and recognition of the fears and emotions of our patients are the basis for excellent patient experience and patient safety”. “Working with Groups I experience as thoroughly fascinating and inspiring. In interaction with groups I am every time amazed by the enormous potential of practical knowledge and direct experience that lies hidden in groups and that is so easily overlooked. Herein lies the basis for excellent vulnerable leadership.

Session Details:

How clinical trial supply managers can reduce the patient burden from a fear reduction perspective

2023-03-15, 3:30 PM

Session Details:

PANEL DISCUSSION: Uncovering new trends and technological advancements for the European clinical supply chain: what’s new for 2023?

2023-03-15, 11:15 AM

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Diana Cocora
Senior Supply Chain Manager, Akamis Bio

Session Details:

Choosing a manufacturing partner: what to consider when selecting a CMO

2023-03-16, 9:00 AM

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Niklas Mattson
Director, Comparator Management, MSD

Session Details:

Effective strategies for sourcing comparators and placebos

2023-03-15, 2:30 PM

Session Details:

PANEL DISCUSSION: Operational agility: the importance of maintaining flexibility in your clinical supply chain

2023-03-16, 11:30 AM

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Daniel Fitzgerald
Director, Clinical Supplies, Galecto Inc

Session Details:

PANEL DISCUSSION: Making a success of direct-to-patient for your clinical trials

2023-03-15, 2:30 PM

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Dr Kamal Amin
Head Of Clinical Supplies Management, Galderma

Session Details:

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

2023-03-16, 2:30 PM

Session Details:

PANEL DISCUSSION: Automation in clinical supply chains: what level of automation can you incorporate?

2023-03-16, 9:00 AM

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Paula Figueiredo
Clinical Supplies Leader, Galapagos

Session Details:

IMP during the Ukrainian conflict: an inspiring story of humanity

2023-03-15, 5:30 PM

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Camillo Rossi
Associate Director, Clinical Trial Material Logistics, Eli Lilly And Company

Session Details:

PANEL DISCUSSION: Running your clinical trial internationally: overcoming logistical challenges to maximise supply chain efficiency

2023-03-15, 3:30 PM

Session Details:

PANEL DISCUSSION: Automation in clinical supply chains: what level of automation can you incorporate?

2023-03-16, 9:00 AM

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Chiranth Hulgur
Senior Manager Clinical Supply Chain Data And Analytics, CSL Behring

Session Details:

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

2023-03-16, 2:30 PM

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Ilaria Rondinone
Clinical Trial Supply Coordinator, Chiesi Group

Session Details:

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

2023-03-16, 2:30 PM

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Philip Oyewale Babatunde Olabode
Senior Manager, Supply Chain And Logistics, Bristol Myers Squibb

Session Details:

Incorporating technology to increase clinical supply chain efficiency

2023-03-15, 4:30 PM

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Gary Cunnington
Global Leader Clinical Trial Supplies Business Consultancy, Boehringer Ingelheim

Session Details:

Harnessing the benefits of e-labelling: accelerating packaging and labelling processes through technological innovation

2023-03-16, 10:00 AM

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Alexandru Marineac
International Logistics Manager, Audubon Biosciences

Session Details:

PANEL DISCUSSION: Running your clinical trial internationally: overcoming logistical challenges to maximise supply chain efficiency

2023-03-15, 3:30 PM

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Laura Gibbons
Director of Business Strategy and Portfolio Management, AstraZeneca

Session Details:

Transforming our supply chain by investing in key capabilities: processes, people and digital

2023-03-15, 8:30 AM

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Sam Mulligan
Digital Lead, Clinical Manufacturing And Supply, AstraZeneca

Session Details:

Transforming our supply chain by investing in key capabilities: processes, people and digital

2023-03-15, 8:30 AM

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Hadar Shaked
Clinical Supply Project Manager, Teva Pharmaceuticals

Session Details:

CASE STUDY: Incorporating e-labelling into your clinical trial supply processes

2023-03-16, 1:00 PM

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Brendan Krause
Head of International, Uber Health
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Henk Dieteren
Clinical Supply Chain Solutions Consultant, Suvoda

Session Details:

PANEL DISCUSSION: Operational agility: the importance of maintaining flexibility in your clinical supply chain

2023-03-16, 11:30 AM

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Landry Giardina
Global Head of Clinical Supply Chain Operations Innovation and Technology, Sanofi

Session Details:

Supply chain efficiency and data driven performance

2023-03-15, 4:30 PM

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Jasmin Hellwig
Associate Director Vendor Relationship Management, MSD

Session Details:

Vendor management: the importance of aligning vendors and sponsors under one shared goal to deliver your trial

2023-03-16, 12:30 PM

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Urtė Fultinavičiūtė
Healthcare Reporter, Clinical Trials Arena, GlobalData Healthcare
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Ulrich Mengel
Associate Director, CTS Business Operations, CSL Behring

Session Details:

PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

2023-03-16, 2:30 PM

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Stefan Dürr
Senior Director, Client Delivery, Cenduit IRT, an IQVIA business, Head of Drug Supply Center of Excellence

Session Details:

Reserved for IQVIA

2023-03-15, 5:00 PM

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Marcel Walraven
Key Account Director, Biocair

Session Details:

Reserved for Biocair

2023-03-16, 9:30 AM

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Marcus Wajngarten
Senior Director, Home Supply, AstraZeneca

Marcus has been realizing innovative solutions and clinical science in the Pharma space for almost 20 years.

Passionate in driving operational value with technology, the science and the patient is always in focus.

As part of AstraZeneca’s Digital Health transformation, he is aiming to bring greater value to patients faster though technology.

Marcus is gearing up AstraZeneca’s capabilities to take on De-centralized trials, with patient centricity at heart.

Session Details:

New Modalities and Their Supply Chain Challenges. CAR-T & Radiopharmaceuticals

2023-03-15, 4:00 PM

Session Details:

PANEL DISCUSSION: Making a success of direct-to-patient for your clinical trials

2023-03-15, 2:30 PM

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Margaret Radford
Unlicensed Medicine Services Manager, Almac

Session Details:

Reserved for Almac

2023-03-15, 12:45 PM

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Plan Your Visit

Venue

NH Milano Congress Centre Strada 2a, Milanofiori, Italy, 20057

Event code: CTSEU23/TCLEU23

Room rate (single): €129 (incl. VAT and breakfast)

Accommodation

Event code: CTSEU23/TCLEU23

Room rate (single): €129 (incl. VAT and breakfast)

Sponsors

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WHAT TO EXPECT FOR 2023?

 

Clinical Trial Supply Europe is the meeting place for the pharmaceutical and biotechnology community to discover how to excel in clinical supply strategy as well as form key connections for long-term success.

See What It's All About

Enquiry

Contact Us

SPONSORSHIP ENQUIRIES

Jaz Sidhu

Senior Sponsorship Manager

+44 (0) 20 7947 2755

SPEAKING OPPORTUNITIES

Louisa Manning

Producer, Clinical Trial Supply Europe

+44 (0) 20 7661 0906

MARKETING ENQUIRIES

Moona Popal

Marketing Manager

SPONSORSHIP ENQUIRIES

To enquire about sponsorship opportunities for the conference, please contact:

Jaz Sidhu

Senior Sponsorship Manager


+44 (0) 20 7947 2755

SPEAKER ENQUIRIES

To enquire about speaking opportunities for the conference, please contact:

Louisa Manning

Producer, Clinical Trial Supply Europe


+44 (0) 20 7661 0906