16th Annual Pharma Anti-Counterfeiting, Serialization & Supply Chain Security 2025
16th Annual Pharma Anti-Counterfeiting, Serialization & Supply Chain 2025
17th & 18th September, 2025
Hilton Washington Dulles Airport, United States
5 Reasons
to attend the event

Knowledge
Gain insights from experts, researchers, and professionals to stay updated on the latest pharma advancements.

Convenience
Attend sessions from anywhere, eliminating travel hassles while accessing high-quality content at your own pace.

Cutting-Edge Insights
Discover the latest trends, innovations, and breakthroughs shaping the future of the pharmaceutical industry.

Networking
Connect with peers, industry leaders, and collaborators to exchange ideas and explore new opportunities.

Practical Takeaways
Walk away with actionable strategies, real-world case studies, and learn best practices to implement in your work.

Knowledge
Gain insights from experts, researchers, and professionals on the latest pharma advancements.

Convenience
Attend sessions from anywhere, eliminate travel hassles & access quality content at your own pace.

Cutting-Edge Insights
Explore the latest trends, innovations, and breakthroughs driving the future of the pharmaceutical industry.

Networking
Connect with peers, industry leaders, and collaborators to exchange ideas and explore new opportunities.

Practical Takeaways
Walk away with practical strategies, case studies, and proven best practices to apply in real-time.
Event Speakers
Download Brochure
Event Schedule
Meet to learn and network with your conference colleagues.
09:00 - Chairperson opening remarks
Speaker

MARK KARHOFF
Principal Consultant, SCM, Life Sciences, Serialization
Ten Count Consulting
09:10 – AI’s Coming Impact on Supply Chain Professionals: Drawing Parallels from Adjacent Industries to Identify Key Skills of the Future
AI & SCM
• What do supply chain leaders, cybersecurity experts, and capital market traders have in common? Uncover the surprising overlap and learn how supply chain professionals can future-proof their careers by adopting the mindset and skills driving success across these high-stakes fields.
• Gain insight into must-have capabilities like AI literacy, data interpretation, and adaptive thinking, which are essential tools for thriving in increasingly autonomous and predictive supply chains.
• Walk away with a future-ready mindset—understand the parallels between supply chain transformation and quantitative finance, and how you can prepare your team for what’s next.

ANTHONY PULEO
Director, Data Science
AstraZeneca
09:40 – Analytical Technologies for the Authentication of Counterfeit Drug Products
ANALYTICAL TECHNOLOGIES
• This presentation will provide insight into ongoing counterfeit trends and describe the roles and responsibilities of BMS in combating drug product counterfeiting.
• Real suspect product investigations submitted to BMS will be highlighted, including counterfeit tablets and biologics.
• Analytical techniques such as microscopy, vibrational spectroscopy (IR, Raman), UV-Vis, and chromatography are typically used during these forensics analyses.
• Portable technologies are also utilized to detect potential counterfeits in the field.
Speaker

BRITTANY HANDZO
Senior Scientist, Forensics & Innovative Technologies
Bristol-Myers Squibb
10:10 – Solution Provider Presentation
For sponsorship opportunities please contact info.uk@virtueinsight.com
10:40 – Morning Networking Coffee / Tea & Discussion
11:10 – Keynote Panel Discussion: Counterfeit Drugs: Challenges & Opportunities for Effective Solutions.
CHALLENGES & OPPORTUNITIES
• Understanding the scale and consequences for public health and patient safety.
• Evaluating existing policies and identifying gaps in enforcement across different regions.
• Assessing vulnerabilities and implementing strategies to protect the pharmaceutical supply chain.
• Exploring tools like blockchain, AI, and advanced serialization to combat counterfeiting.
• Discussing the financial toll on healthcare systems and the ethical considerations in combating counterfeit drugs.
• Cross-Sector Collaboration – Highlighting the role of partnerships among governments, pharmaceutical companies, NGOs, and tech providers.
• Developing strategies to raise awareness about counterfeit drugs and their risks
Moderator

MARK KARHOFF
Principal Consultant, SCM, Life Sciences Serialization
Ten Count Consulting
Panellists

SCOTT HUFFMAN
Associate Director, Forensics & Innovative Technologies
Bristol-Myers Squibb

SCOTT OULTON
Chief of Forensics
Drug Enforcement Administration

JOHN SCHETTINI
Supply Chain Director
Bayshore Pharmaceuticals

MICHAEL STEPANOVIC
Assistant Professor
UNC Eshelman
12:00 – Revolutionizing Manufacturing: Your Strategic Guide to Embracing Industry 4.0
MANUFACTURING – INDUSTRY 4.0
• Maximizing Manufacturing Efficiency
• Using advanced analytics to foresee equipment issues and minimize downtime
• Implementing real-time monitoring and analytics to ensure product consistency and regulatory compliance
• Adapting production processes to enable smallbatch, patient-specific drug manufacturing
• Reducing waste and optimizing energy use through eco-friendly production methods
• Innovations like blockchain, quantum computing, and advanced biomanufacturing shaping the next phase of pharma production
12:30 – Networking luncheon
13:20 – Keynote Panel Discussion: Streamlining Success: Advanced Supply Chain Strategies for Pharma
SUPPLY CHAIN STRAGIES
• Current trends, challenges, and opportunities in the pharmaceutical supply chain for betterment
• Strategies to identify, mitigate, and manage risks, including disruptions, regulatory compliance, and quality control
• Best practices for balancing supply and demand while minimizing waste and costs
• Integrating eco-friendly processes to meet global sustainability goals
• Building strong partnerships with suppliers, distributors, and other stakeholders for seamless operations
• Emerging technologies and strategies shaping the future of pharmaceutical supply chains
Moderator

MARK KARHOFF
Principal Consultant, SCM, Life Sciences
Serialization, Ten Count Consulting
Panellists

MAHFUZA AHMEDIN
Director, Packaging Tech Transfer & Validation
AstraZeneca

VICKRAM SRIVASTAVA
NJ, Head of Supply Chain – North America
Sun Pharma

HARRY GREEN
Global Manufacturing Operations Senior Leader
SupplyChain & Enterprise Lean Transformation
Novavax

MICHAL NOWINA KONOPKA
Director US Supply Chain
Kedrion Biopharma
14:10 - Lessons Learnt from GMP Compliance in Emerging Markets
Speaker

EYAD SALMAN
Principle Manager
Genentech
14:40 – How Augmented Reality is Revolutionizing Pharmaceutical Packaging?
AR
• Minimize Errors, Maximize Efficiency: Leverage AR technology to reduce human errors and enhance operational precision in pharmaceutical packaging processes.
• Compliance Meets Innovation: Ensure adherence to stringent regulatory standards by seamlessly integrating AR into critical workflows.
• Elevating Quality and Integrity: Safeguard product quality while streamlining operations with cutting-edge AR-driven solutions.
• With AR-driven tracking and monitoring, stakeholders gain better control and transparency across the packaging process
• AR integrates compliance checks into workflows, ensuring adherence to stringent pharmaceutical regulations
• By reducing errors and waste, AR optimizes resource usage, ultimately lowering operational costs
Speaker

HUMBERTO VEGA
Chemical Engineer
Retired, Former JnJ
15:10 - Afternoon Networking Coffee / Tea & Discussion
15:40 – Recent Federal and State Enforcement Efforts Pertaining to Supply Chain Security
This presentation will provide an overview of laws used to enforce supply chain security, including enforcement of the Drug Supply Chain Security Act and the SAFE DOSES Act, as well as a survey of recent federal enforcement actions and nationwide supply chain enhancement used in the accreditation process.
Panellists

ANDREW J. HULL
Director, FDA, DEA, & Healthcare Enforcement Litigator
Hyman Phelps & McNamara

KARLA L. PALMER
Director, FDA and DEA Investigations
Hyman Phelps & McNamara
16:10 – Panel Discussion: Regulatory Frontlines: Global Updates and Strategies to Combat Counterfeit Drugs
REGULATORY
• Global Regulatory Requirements: Navigating compliance standards across regions, including the EU (FMD) and the U.S. (DSCSA).
• Recent Regulatory Developments: Highlighting updates from key global frameworks
• Exploring how different countries and regions address counterfeit drugs through legislation and enforcement.
• Discussing the importance of aligning regulatory measures to ensure global consistency.
• Evaluating the effectiveness of regulatory actions through monitoring and reporting mechanisms.
• Identifying unique issues faced by low- and middle-income countries and potential solutions.
• Exploring collaborations between regulators, industry players, and international organizations to strengthen anti-counterfeiting efforts.
Moderator

RAM BALANI
CEO/Founder
eSTARHelper
Panellists

ANNA LUCZAK
Director, Regulatory Affair and Patient Safety
McKesson

TRACY NASARENKO
VP of Community Engagement, Healthcare
GS1

ALADIN ALKHAWAM,
Former Director Global Serialization
Par Pharmaceutical
17:00 – Closing remarks by chairperson and End of day 01 conference
17:10 – 18:15 – Networking Drinks
09:00 - Chairperson opening remarks
Speaker

MARK KARHOFF
Principal Consultant, SCM, Life Sciences, Serialization
Ten Count Consulting
09:10 – AI’s Coming Impact on Supply Chain Professionals: Drawing Parallels from Adjacent Industries to Identify Key Skills of the Future
AI & SCM
• What do supply chain leaders, cybersecurity experts, and capital market traders have in common? Uncover the surprising overlap and learn how supply chain professionals can future-proof their careers by adopting the mindset and skills driving success across these high-stakes fields.
• Gain insight into must-have capabilities like AI literacy, data interpretation, and adaptive thinking, which are essential tools for thriving in increasingly autonomous and predictive supply chains.
• Walk away with a future-ready mindset—understand the parallels between supply chain transformation and quantitative finance, and how you can prepare your team for what’s next.

ANTHONY PULEO
Director, Data Science
AstraZeneca
09:40 – Analytical Technologies for the Authentication of Counterfeit Drug Products
ANALYTICAL TECHNOLOGIES
• This presentation will provide insight into ongoing counterfeit trends and describe the roles and responsibilities of BMS in combating drug product counterfeiting.
• Real suspect product investigations submitted to BMS will be highlighted, including counterfeit tablets and biologics.
• Analytical techniques such as microscopy, vibrational spectroscopy (IR, Raman), UV-Vis, and chromatography are typically used during these forensics analyses.
• Portable technologies are also utilized to detect potential counterfeits in the field.
Speaker

BRITTANY HANDZO
Senior Scientist, Forensics & Innovative Technologies
Bristol-Myers Squibb
10:10 – Solution Provider Presentation
For sponsorship opportunities please contact info.uk@virtueinsight.com
10:40 – Morning Networking Coffee / Tea & Discussion
11:10 – Keynote Panel Discussion: Counterfeit Drugs: Challenges & Opportunities for Effective Solutions.
CHALLENGES & OPPORTUNITIES
• Understanding the scale and consequences for public health and patient safety.
• Evaluating existing policies and identifying gaps in enforcement across different regions.
• Assessing vulnerabilities and implementing strategies to protect the pharmaceutical supply chain.
• Exploring tools like blockchain, AI, and advanced serialization to combat counterfeiting.
• Discussing the financial toll on healthcare systems and the ethical considerations in combating counterfeit drugs.
• Cross-Sector Collaboration – Highlighting the role of partnerships among governments, pharmaceutical companies, NGOs, and tech providers.
• Developing strategies to raise awareness about counterfeit drugs and their risks
Moderator

MARK KARHOFF
Principal Consultant, SCM, Life Sciences Serialization
Ten Count Consulting
Panellists

SCOTT HUFFMAN
Associate Director, Forensics & Innovative Technologies
Bristol-Myers Squibb

SCOTT OULTON
Chief of Forensics
Drug Enforcement Administration

JOHN SCHETTINI
Supply Chain Director
Bayshore Pharmaceuticals

MICHAEL STEPANOVIC
Assistant Professor
UNC Eshelman
12:00 – Revolutionizing Manufacturing: Your Strategic Guide to Embracing Industry 4.0
MANUFACTURING – INDUSTRY 4.0
• Maximizing Manufacturing Efficiency
• Using advanced analytics to foresee equipment issues and minimize downtime
• Implementing real-time monitoring and analytics to ensure product consistency and regulatory compliance
• Adapting production processes to enable smallbatch, patient-specific drug manufacturing
• Reducing waste and optimizing energy use through eco-friendly production methods
• Innovations like blockchain, quantum computing, and advanced biomanufacturing shaping the next phase of pharma production
12:30 – Networking luncheon
13:20 – Keynote Panel Discussion: Streamlining Success: Advanced Supply Chain Strategies for Pharma
SUPPLY CHAIN STRAGIES
• Current trends, challenges, and opportunities in the pharmaceutical supply chain for betterment
• Strategies to identify, mitigate, and manage risks, including disruptions, regulatory compliance, and quality control
• Best practices for balancing supply and demand while minimizing waste and costs
• Integrating eco-friendly processes to meet global sustainability goals
• Building strong partnerships with suppliers, distributors, and other stakeholders for seamless operations
• Emerging technologies and strategies shaping the future of pharmaceutical supply chains
Moderator

MARK KARHOFF
Principal Consultant, SCM, Life Sciences
Serialization, Ten Count Consulting
Panellists

MAHFUZA AHMEDIN
Director, Packaging Tech Transfer & Validation
AstraZeneca

VICKRAM SRIVASTAVA
NJ, Head of Supply Chain – North America
Sun Pharma

HARRY GREEN
Global Manufacturing Operations Senior Leader
SupplyChain & Enterprise Lean Transformation
Novavax

MICHAL NOWINA KONOPKA
Director US Supply Chain
Kedrion Biopharma
14:10 - Lessons Learnt from GMP Compliance in Emerging Markets
Speaker

EYAD SALMAN
Principle Manager
Genentech
14:40 – How Augmented Reality is Revolutionizing Pharmaceutical Packaging?
AR
• Minimize Errors, Maximize Efficiency: Leverage AR technology to reduce human errors and enhance operational precision in pharmaceutical packaging processes.
• Compliance Meets Innovation: Ensure adherence to stringent regulatory standards by seamlessly integrating AR into critical workflows.
• Elevating Quality and Integrity: Safeguard product quality while streamlining operations with cutting-edge AR-driven solutions.
• With AR-driven tracking and monitoring, stakeholders gain better control and transparency across the packaging process
• AR integrates compliance checks into workflows, ensuring adherence to stringent pharmaceutical regulations
• By reducing errors and waste, AR optimizes resource usage, ultimately lowering operational costs
Speaker

HUMBERTO VEGA
Chemical Engineer
Retired, Former JnJ
15:10 - Afternoon Networking Coffee / Tea & Discussion
15:40 – Recent Federal and State Enforcement Efforts Pertaining to Supply Chain Security
This presentation will provide an overview of laws used to enforce supply chain security, including enforcement of the Drug Supply Chain Security Act and the SAFE DOSES Act, as well as a survey of recent federal enforcement actions and nationwide supply chain enhancement used in the accreditation process.
Panellists

ANDREW J. HULL
Director, FDA, DEA, & Healthcare Enforcement Litigator
Hyman Phelps & McNamara

KARLA L. PALMER
Director, FDA and DEA Investigations
Hyman Phelps & McNamara
16:10 – Panel Discussion: Regulatory Frontlines: Global Updates and Strategies to Combat Counterfeit Drugs
REGULATORY
• Global Regulatory Requirements: Navigating compliance standards across regions, including the EU (FMD) and the U.S. (DSCSA).
• Recent Regulatory Developments: Highlighting updates from key global frameworks
• Exploring how different countries and regions address counterfeit drugs through legislation and enforcement.
• Discussing the importance of aligning regulatory measures to ensure global consistency.
• Evaluating the effectiveness of regulatory actions through monitoring and reporting mechanisms.
• Identifying unique issues faced by low- and middle-income countries and potential solutions.
• Exploring collaborations between regulators, industry players, and international organizations to strengthen anti-counterfeiting efforts.
Moderator

RAM BALANI
CEO/Founder
eSTARHelper
Panellists

ANNA LUCZAK
Director, Regulatory Affair and Patient Safety
McKesson

TRACY NASARENKO
VP of Community Engagement, Healthcare
GS1

ALADIN ALKHAWAM,
Former Director Global Serialization
Par Pharmaceutical
17:00 – Closing remarks by chairperson and End of day 01 conference
17:10 – 18:15 – Networking Drinks
09:00 - Chairperson opening remarks
Speaker

PABLO MEDINA
Principal, Operations Strategy, Serialization & DSCSA
Ten Count Consulting
09:10 – DEA controls in the manufacturing equipment sector primarily those involving tableting and encapsulating equipment to include dies, molds, critical parts, etc
TACKLING COUNTERFEIT DRUGS
Speaker

TODD BOYETT
Chemical Investigations Section, Diversion Control Division,
Drug Enforcement Administration
09:40 – Pioneering Innovations and Best Practices in Pharma Logistics
LOGISTICS / COLD STORAGE
• Ensuring adherence to global standards for safety, quality, and transportation of pharmaceutical products
• Strategies to address temperature excursions, supply disruptions, and logistical challenges
• Exploring cutting-edge solutions for temperature stability and product protection
• Implementing eco-friendly practices to reduce the environmental impact of cold chain logistics
• Enhancing transparency and accountability through advanced tracking and reporting systems
• Emerging technologies and innovations set to redefine the landscape of pharmaceutical logistics
Speaker

HUMBERTO VEGA
Chemical Engineer
Retired, Former JnJ
10:10 – Solution Provider Presentation
For sponsorship opportunities please contact
info.uk@virtueinsight.com
10:40 – Morning Networking Coffee / Tea & Discussion
11:10 - Panel Discussion with the experts - Serialization, Track & Trace - Compliance & Implementation
SERIALIZATION – TRACK & TRACE
• Role of Serialization in Fighting Counterfeits: Unique ways to enhance supply chain security.
• Challenges in Implementation: Addressing technical, operational, and financial hurdles in adopting serialization and track-and-trace systems.
• Strategies to ensure seamless collaboration between manufacturers, distributors, and retailers.
• Protecting sensitive data while maintaining transparency and compliance.
• Discussing emerging trends and their potential to revolutionize pharmaceutical supply chain management.
• What are the current requirements to follow in serialisation? How to ensure that you are up to date with all global traceability regulations?
Moderator

PABLO MEDINA
Principal, Operations Strategy, Serialization & DSCSA
Ten Count Consulting
Panellists

SENTHIL RAJARATNAM
Senior Director, Global Packaging
Eli Lilly

PAULE BELONY
Director, Packaging Product Security & Traceability
AstraZeneca

NICK VYAS
Executive Director
USC Marshall Center for Global SCM

GREGORY GOGER
Global Traceability Lead
Abbvie

ERIC MARSHALL
Principal
Leavitt Partners
12:00 – Topic TBC

ANDREY ATANASOV
Director Business Development and Sales
SoftGroup
12:30 –Networking luncheon
13:30 – Digital Accessibility in Pharma Serialization & Supply Chain
DIGITAL ACCESSIBILITY

STEPHEN FRAMIL
Corporate Global Head of Accessibility
Merck
14:00 - Panel Discussion with the experts – “Revolutionizing Pharma Supply Chains: Unlocking the Power of Emerging Technologies”
IMPACT OF TECHNOLOGY
• Using AI to forecast demand, optimize inventory, and predict disruptions in the supply chain.
• Leveraging blockchain to improve data integrity, traceability, and combat counterfeiting in pharmaceutical distribution
• Bridging the Gap: Digital Accessibility in the Modern Supply Chain
• How the Internet of Things (IoT) enables real-time tracking, monitoring, and enhanced visibility across the supply chain
• How robotic systems streamline storage, picking, and packing processes, reducing human error and improving speed
• Analyzing large datasets to gain actionable insights, optimize routes, and improve decision making across the supply chain
• Ensuring the integrity of temperature-sensitive drugs through real-time temperature monitoring and automatedalerts
• A look at upcoming technologies – Where are we heading?
Moderator

HEATHER LEIGH FLANNERY
CEO
AI MINDSystems Foundation
Panellists

ANTHONY PULEO
Director, Data Science
AstraZeneca

STEPHEN FRAMIL
Corporate Global Head of Accessibility
Merck

LENORA DIEYI
Investigator, Modeling & Simulation
GSK
14:50 – Closing remarks by chairperson and End of day conference
09:00 - Chairperson opening remarks
Speaker

PABLO MEDINA
Principal, Operations Strategy, Serialization & DSCSA
Ten Count Consulting
09:10 – DEA controls in the manufacturing equipment sector primarily those involving tableting and encapsulating equipment to include dies, molds, critical parts, etc
TACKLING COUNTERFEIT DRUGS
Speaker

TODD BOYETT
Chemical Investigations Section, Diversion Control Division,
Drug Enforcement Administration
09:40 – Pioneering Innovations and Best Practices in Pharma Logistics
LOGISTICS / COLD STORAGE
• Ensuring adherence to global standards for safety, quality, and transportation of pharmaceutical products
• Strategies to address temperature excursions, supply disruptions, and logistical challenges
• Exploring cutting-edge solutions for temperature stability and product protection
• Implementing eco-friendly practices to reduce the environmental impact of cold chain logistics
• Enhancing transparency and accountability through advanced tracking and reporting systems
• Emerging technologies and innovations set to redefine the landscape of pharmaceutical logistics
Speaker

HUMBERTO VEGA
Chemical Engineer
Retired, Former JnJ
10:10 – Solution Provider Presentation
For sponsorship opportunities please contact
info.uk@virtueinsight.com
10:40 – Morning Networking Coffee / Tea & Discussion
11:10 - Panel Discussion with the experts - Serialization, Track & Trace - Compliance & Implementation
SERIALIZATION – TRACK & TRACE
• Role of Serialization in Fighting Counterfeits: Unique ways to enhance supply chain security.
• Challenges in Implementation: Addressing technical, operational, and financial hurdles in adopting serialization and track-and-trace systems.
• Strategies to ensure seamless collaboration between manufacturers, distributors, and retailers.
• Protecting sensitive data while maintaining transparency and compliance.
• Discussing emerging trends and their potential to revolutionize pharmaceutical supply chain management.
• What are the current requirements to follow in serialisation? How to ensure that you are up to date with all global traceability regulations?
Moderator

PABLO MEDINA
Principal, Operations Strategy, Serialization & DSCSA
Ten Count Consulting
Panellists

SENTHIL RAJARATNAM
Senior Director, Global Packaging
Eli Lilly

PAULE BELONY
Director, Packaging Product Security & Traceability
AstraZeneca

NICK VYAS
Executive Director
USC Marshall Center for Global SCM

GREGORY GOGER
Global Traceability Lead
Abbvie

ERIC MARSHALL
Principal
Leavitt Partners
12:00 – Topic TBC

ANDREY ATANASOV
Director Business Development and Sales
SoftGroup
12:30 –Networking luncheon
13:30 – Digital Accessibility in Pharma Serialization & Supply Chain
DIGITAL ACCESSIBILITY

STEPHEN FRAMIL
Corporate Global Head of Accessibility
Merck
14:00 - Panel Discussion with the experts – “Revolutionizing Pharma Supply Chains: Unlocking the Power of Emerging Technologies”
IMPACT OF TECHNOLOGY
• Using AI to forecast demand, optimize inventory, and predict disruptions in the supply chain.
• Leveraging blockchain to improve data integrity, traceability, and combat counterfeiting in pharmaceutical distribution
• Bridging the Gap: Digital Accessibility in the Modern Supply Chain
• How the Internet of Things (IoT) enables real-time tracking, monitoring, and enhanced visibility across the supply chain
• How robotic systems streamline storage, picking, and packing processes, reducing human error and improving speed
• Analyzing large datasets to gain actionable insights, optimize routes, and improve decision making across the supply chain
• Ensuring the integrity of temperature-sensitive drugs through real-time temperature monitoring and automatedalerts
• A look at upcoming technologies – Where are we heading?
Moderator

HEATHER LEIGH FLANNERY
CEO
AI MINDSystems Foundation
Panellists

ANTHONY PULEO
Director, Data Science
AstraZeneca

STEPHEN FRAMIL
Corporate Global Head of Accessibility
Merck

LENORA DIEYI
Investigator, Modeling & Simulation
GSK
14:50 – Closing remarks by chairperson and End of day conference
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Event Testimonials
A huge thanks to all our sponsors, attendees and partners!
“It was a very well-run event, very much serialisation and brand protection orientated so good for those interested in those particular streams.”
“The conference was well organised and informative. It was just the right size to engage with presenters and also get to know other attendees better.”
“Very enjoyable and informative ”
Venue details
The venue is easily accessible, well-equipped with modern amenities, and offers a comfortable, professional setting for all attendees.
Venue
Hilton Washington
Dulles Airport, USA
13869 Park Center Rd,
Herndon, VA 20171,
United States
+1 703-478-2900
Venue – Hilton Washington Dulles Airport, USA
13869 Park Center Rd,
Herndon, VA 20171,
United States
+1 703-478-2900