Global Contact Center

Unser erstklassiges Contact Center ist spezialisiert auf Unternehmen in den Bereichen Medizin, Pharmazie und Biologie und rund um die Uhr, 365 Tage im Jahr, erreichbar.

200

MAH-Partnerschaften

Schließen Sie sich mehr als 200 angesehenen Marketing Authorization Holdern (MAHs) an, die auf unsere Expertise und erstklassige Dienstleistungen unseres Contact Centers vertrauen und so eine nachhaltige und erfolgreiche Partnerschaft eingegangen sind.

10000

Medizinprodukte

Bewältigen Sie problemlos die Komplexität produktbezogener Anfragen. Wir bearbeiten täglich global Anfragen zu mehr als 10.000 Produkten. Ihre Kund*innen können auf präzise und schnelle Informationen vertrauen.

500000

Anfragen pro Jahr

Verlassen Sie sich auf unsere Erfahrung und Expertise, um auch hohe Anfragevolumen zu bewältigen – mit über einer halben Million bearbeiteter Anfragen jährlich. Die Kommunikation mit Ihren Kund*innen ist bei uns in kompetenten Händen.

Best-in-Class Global Contact Center Services

Global contact center support icon

Contact Center - 24/7/365

Profitieren Sie von lückenloser Unterstützung durch unser Contact Center, das rund um die Uhr, 365 Tage im Jahr, verfügbar ist, um Ihre Kund*innen jederzeit, sowohl tagsüber...

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Contact Center - 24/7/365

Profitieren Sie von lückenloser Unterstützung durch unser Contact Center, das rund um die Uhr, 365 Tage im Jahr, verfügbar ist, um Ihre Kund*innen jederzeit, sowohl tagsüber als auch nachts, zu ünterstützen.

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Erreichbarkeit in mehr als 35 Sprachen

Überwinden Sie Sprachbarrieren mit Hilfe unseres multilingualen Teams. Wir bieten diesen Service in mehr als 35 Sprachen und gewährleisten so ein reibungslose...

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Erreichbarkeit in mehr als 35 Sprachen

Überwinden Sie Sprachbarrieren mit Hilfe unseres multilingualen Teams. Wir bieten diesen Service in mehr als 35 Sprachen und gewährleisten so ein reibungslose Kommunkation mit Ihrer internationalen Kundschaft.

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Partnerschaften von durchscnnittlich mehr als 10 Jahren

Bauen Sie langfristige Beziehungen mit einem Partner auf, der sich über die Jahre bewährt hat. Die Zusammenarbeit mit unseren Kund*innen ist...

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Partnerschaften von durchscnnittlich mehr als 10 Jahren

Bauen Sie langfristige Beziehungen mit einem Partner auf, der sich über die Jahre bewährt hat. Die Zusammenarbeit mit unseren Kund*innen ist von Dauer, durchschnittlich über 10 Jahre und spiegelt das Vertrauen und die Zuverlässigkeit wider, die unsere Partnerschaften auszeichnen.

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Globaler Contact Center Support

Durch unsere weltweit strategisch positionierten und nahtlos integrierten Contact Center bieten wir maßgeschneiderte Lösungen, die den Anforderungen von Unternehmen jeder Größe gerecht werden. Unser erfahrenes Team von Contact Center-Expert*innen steht bereit und unterstützt Sie bestmöglich in den Bereichen

Unsere globalen Contact-Center-Dienste bieten pharmazeutischen Unternehmen rund um die Uhr Unterstützung. Unser Team setzt sich aus erfahrenen Apotheker*innen, Pflegekräften und anderen Gesundheitsfachkräften (Health Care Provider, HCP), Absolvent*innen der Lebenswissenschaften sowie qualifizierten Kundenservice-Mitarbeiternden zusammen. Sie fungieren als Erweiterung Ihres Teams, übermitteln wichtige Produktinformationen in den Bereichen Arzneimittel-/Geräteinformationen sowie Produktsicherheit und übernehmen die Patient*innenbetreuung und kommerzielle Dienstleistungen.

Customer service professional in a contact center wearing headset asking a coworker-a-question
Several business professionals having fun at a business meeting

Zuverlässige und erstklassige Lösungen

Das globale Contact Center spielt eine zentrale Rolle in Pharma- und Gesundheitsunternehmen, denn es muss präzise und schnell Informationen für medizinische Fachkräfte, Patient*innen und die Öffentlichkeit bereitstellen. Eingehende Anfragen werden, unabhängig von ihrer Komplexität, nach Dringlichkeit und Art priorisiert und von unserem spezialisierten Team detailliert beantwortet und dokumentiert.

Unsere spezialisierten Fachkräfte (Subject Matter Experts, SMEs) und unsere medizinische Redaktion sind bestens darauf vorbereitet, maßgeschneiderte Antworten zu erstellen. Durch den Einsatz verschiedener Kommunikationskanäle liefert das Contact Center Informationen an Gesundheitsdienstleister, Patient*innen und andere Stakeholder und hält dabei strengste regulatorische Richtlinien und Vertraulichkeitsstandards ein. Kontinuierliche Schulungen und Qualitätskontrollmaßnahmen werden eingesetzt, um höchste Servicestandards zu gewährleisten. So wird unser globales Contact Center zu einer unverzichtbaren Ressource für die präzise und zuverlässige Weitergabe von Produktinformationen sowie die schnelle Betreuung von Patient*innen.

Contact-Center-Standorte weltweit

US UK and Europe Asia Pacific

North America

europe

Asia Pacific

Raleigh (HQ) 

107 West Hargett St.
Raleigh, NC 27601

1-888-242-0559

Berlin 

Siemensdamm 62
13627 Berlin

+49 (0) 30 85606878 - 0

North Yorkshire

Thomas House,
Olliver, Aske, Richmond
North Yorkshire, DL10 5HX

+44 (0)1748 828800

Melbourne (Hawthorn) 

Suite 6, Ground Level
452 Johnston Street
Abbotsford, VIC 3067

+61 3 8814 7900

Hyderabad

2nd Floor, South Wing
JVP SOFT
No 5, Software Units Layout
Madhapur, Hyderabad- 500 081
Telangana, India

+91 966 611 1980

Tokyo 

5-27-5 Sendagaya, Shibuya-ku (suite 13-101, 13-102, 13-113, 13-130)

+81 3 6277 4041

Makati City

7th Floor Office F
Armstrong Corporate Center
HV Dela Costa Ave.
Salcedo Village
Makati City

+61 38814 7900

Shanghai

Room 04N162, 4/F, Annex
No. 138 Huaihai Middle Road
Huangpu District
Shanghai

+61 38814 7900

Contact-Center-Standorte weltweit

US

Down arrow - click here to expand section.
Raleigh (HQ) 

107 West Hargett St.
Raleigh, NC 27601

1-888-242-0559

UK and Europe

Down arrow - click here to expand section.
Berlin 

Siemensdamm 62
13627 Berlin

+49 (0) 30 85606878 - 0

North Yorkshire

Thomas House,
Olliver, Aske, Richmond
North Yorkshire, DL10 5HX

+44 (0)1748 828800

Asia Pacific

Down arrow - click here to expand section.
Melbourne (Hawthorn) 

Suite 6, Ground Level
452 Johnston Street
Abbotsford, VIC 3067

+61 3 8814 7900

Hyderabad

2nd Floor, South Wing
JVP SOFT
No 5, Software Units Layout
Madhapur, Hyderabad- 500 081
Telangana, India

+91 966 611 1980

Tokyo 

5-27-5 Sendagaya, Shibuya-ku (suite 13-101, 13-102, 13-113, 13-130)

+81 3 6277 4041

Makati City

7th Floor Office F
Armstrong Corporate Center
HV Dela Costa Ave.
Salcedo Village
Makati City

+61 38814 7900

Shanghai

Room 04N162, 4/F, Annex
No. 138 Huaihai Middle Road
Huangpu District
Shanghai

+61 38814 7900

Global Contact Center Experts

  • Rajul Jain Bio Photo

    Rajul Jain

    President, Medical Information

    View Bio

  • Dave Bezick Bio Photo

    Dave Bezick

    Senior Director, Medical Information

    View Bio

  • Hannah Hunter Bio Photo

    Hannah Hunter

    Senior Director, Medical Information

    View Bio

  • Katie Tonge Bio Photo

    Katie Tonge

    Senior Director, Medical Information

    View Bio

  • Leanne Shaw Bio Photo

    Leanne Shaw

    Senior Director, Medical Information

    View Bio

  • Valerie Huh Bio Photo

    Valerie Huh

    Director, Global Innovation and Implementation

    View Bio

  • Victoria Evans Bio Photo

    Victoria Evans

    Director, Medical Information

    View Bio

  • Emily Bevington Bio Photo

    Emily Bevington

    Associate Director, Global Innovation and Implementation

    View Bio

  • Ana Ming Bio Photo

    Ana Ming

    Senior Global Innovation and Implementation Manager

    View Bio

Rajul Jain has over 20 years of international experience in Medical Information (MI), Pharmacovigilance (PV), Technology, and Program Management. With an extensive educational background including an MBA, Engineering degree, PMP, Medical Affairs Competency Certificate (ACMA), and various other healthcare certifications, she brings a wealth of knowledge to her roles. She is currently President of Medical Information in ProPharma with responsibility for oversight and expansion of global contact center operations. Prior to this, she managed all of the MI programs for IQVIA and technology and automation solutions for MI/PV programs. Rajul is passionate about improving business processes and fostering innovative solutions in the healthcare and pharmaceutical industry.

Dave brings over 15 years of Medical Information Contact Center Management and Operations experience. A licensed Registered Nurse, he began his career as a front-line Medical Information Specialist and has continually advanced into roles of increasing responsibility within the Medical Affairs industry. He is currently the Senior Director, Medical Information Service Delivery (Operations and Account Management) at ProPharma. Dave's passion for the patient and HCP experience is evident in his approach to staff selection, employee development and operational excellence of his teams.

Hannah is the Senior Director of Medical Information (MI), Europe at ProPharma, where she leads dedicated client services across the continent. With 18 years of experience in Medical Information, Hannah has supported pharmaceutical companies globally. She is passionate about the evolution of MI to better meet the needs of customers and clients. As a proven leader, Hannah excels in guiding and inspiring her team to achieve excellence. She places a strong emphasis on the provision of telephone-based MI, recognizing its importance as the primary channel for MI inquiries and its potential for excellent service delivery. Additionally, she is focused on leveraging technology to enhance the efficiency and effectiveness of medical information teams.

Katie has over 16 years of Medical Information outsourcing experience, as well as contact centre management, and is passionate about using Medical Information to improve the health and safety of patients. She enjoys working with clients to suggest innovative and commercially sustainable options for their Medical Information needs. She has a track record of establishing service levels and KPIs with clients to ensure the highest standards for customers.  She also has Project Management experience in helping clients transition from in-sourced services to an outsourced Medical information solution.

Leanne brings 15 years of Medical Information Contact Center Management and Operations experience across Europe and Asia Pacific. Leanne begun her career in this space as a UK Medical Information Specialist and has continually advanced into roles of increasing responsibility including client management, operations management, and project leadership. Leanne is currently the Senior Director of Medical Information Services for JAPAC at ProPharma. Leanne’s key focus on service evolution and customer excellence helps deliver JAPAC services to the highest standard of success.

Valerie Huh brings over 20 years of experience in the pharmaceutical and healthcare industries, with expertise in global operations and process improvements. She holds a Doctor of Pharmacy (Pharm.D.), a degree in Chemistry, and an MBA with a certificate in business analytics. In her current role, she leads innovation and technology enablement in Medical Information and supports business expansions, driving forward strategic initiatives to enhance service quality and operational efficiency.

Victoria Evans is a seasoned professional with over 10 years of experience in the Medical Information (MI) field. As the Director of Client Services at ProPharma, she leads a global team of Implementation and Client Account Managers, ensuring the successful onboarding, implementation, and maintenance of MI clients worldwide. Victoria holds a BSc in Psychology and has furthered her education with a Graduate Diploma in Law and a Legal Practice Certificate. Her passion for project management and patient safety drives her to find innovative solutions, and her focus and excellent project skills consistently help clients achieve their goals.
Emily Bevington has 9 years of experience in Medical Information Operations and Program and Project Management. She has studied BSc Biological Sciences and MSc Artificial Intelligence. With a background in technology and programming, she is competent in the design, development and deployment of technology solutions, with a particular focus on Data Science, Artificial Intelligence and Machine Learning.

Ana Ming is a highly skilled pharmacist based in Australia, with 12+ years of experience in the pharmaceutical services and healthcare industries. Currently at ProPharma, she brings expertise in medical information management, patient care, and regulatory compliance. Additionally, Ana is a certified Justice of the Peace (JP), combining her healthcare experience with a commitment to community service and ethical leadership. Her collaborative approach, coupled with a focus on innovative solutions, makes her a valuable asset in optimizing patient outcomes and advancing pharmaceutical practices.

News & Insights

AI in PV Surveillance: Aligning Innovation with Regulatory Expectations

Februar 2, 2026

AI in PV Surveillance: Aligning Innovation with Regulatory Expectations

Explore how AI is transforming pharmacovigilance while ensuring patient safety, data integrity, and regulatory compliance with insights from the 2025 CIOMS report.

Preparing for eCTD 4.0: What FDA Submitters Need to Know

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Preparing for eCTD 4.0: What FDA Submitters Need to Know

eCTD 4.0 is coming. Learn what’s changing, why early planning matters, and how FDA submitters can prepare for a smooth transition.

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outsourcing, and Quality Assurance

Januar 26, 2026

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outs...

Discover how pharmaceutical and biotech companies can elevate laboratory compliance in 2026 through GLP, strategic outsourcing, and robust quality assurance.

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero Targets

Januar 27, 2026

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero T...

ProPharma’s greenhouse gas reduction targets are validated by SBTi, aligning with the Net-Zero Standard and a commitment to reach net-zero by 2050.

ProPharma Expands Operations with New Office in Hyderabad

Dezember 11, 2025

ProPharma Expands Operations with New Office in Hyderabad

ProPharma expands with a new office in Hyderabad, enhancing innovation and growth in regulatory, clinical, and compliance services for the life sciences industry.

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

Dezember 4, 2025

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

ProPharma taps Daniel Ryan as President of Clinical Research Solutions, strengthening its clinical trial management leadership and expanding its FSP Solutions.

ProPharma Recognized for AI Excellence at ECCCSA

Januar 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

Oktober 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Case Study Setting up a Global PV System - ProPharma

Februar 5, 2026

Setting up a Global PV System

A company needed to rapidly establish a fully compliant global pharmacovigilance (PV) system, including UK/EU QPPV coverage, to meet regulatory requirements by a fixed deadline. With safety data and...

Case Study High-Volume Global Pharmacovigilance Onboarding - ProPharma

Januar 30, 2026

High-Volume Global Pharmacovigilance Onboarding

A global biotechnology sponsor faced a sudden surge in pharmacovigilance demand, with monthly ICSR volumes exceeding 30,000 cases across multiple regions. Limited internal capacity, tight onboarding...

Case Study Stabilizing High-Volume Legal Case Processing Through Structured Governance - ProPharma

Januar 28, 2026

Stabilizing High-Volume Legal Case Processing Through Structured Governance

ProPharma’s client faced escalating operational risk as high-volume legal case documentation overwhelmed their prior vendor. Thousands of documents, missed regulatory timelines, and a surge of...

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

März 12, 2026

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

Uncover the intricacies of Pharmacovigilance System Master File (PSMF) management and explore proven strategies to ensure inspection readiness, effective MAH oversight, and regulatory compliance...

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

Februar 17, 2026

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

With promotional scrutiny increasing around areas such as social media, influencer campaigns, direct-to-consumer (DTC) messaging, and data-driven claims, the session walks through the characteristics...

Scaling High-Quality Medical Information Through Offshoring

Februar 11, 2026

Scaling High-Quality Medical Information Through Offshoring

Navigate the complexities of offshoring Medical Information and explore proven strategies to ensure consistent quality, regulatory compliance, and seamless global execution. Join us for an...

News & Insights

AI in PV Surveillance: Aligning Innovation with Regulatory Expectations

February 2, 2026

AI in PV Surveillance: Aligning Innovation with Regulatory Expectations

Explore how AI is transforming pharmacovigilance while ensuring patient safety, data integrity, and regulatory compliance with insights from the 2025 CIOMS report.

Preparing for eCTD 4.0: What FDA Submitters Need to Know

January 29, 2026

Preparing for eCTD 4.0: What FDA Submitters Need to Know

eCTD 4.0 is coming. Learn what’s changing, why early planning matters, and how FDA submitters can prepare for a smooth transition.

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outsourcing, and Quality Assurance

January 26, 2026

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outs...

Discover how pharmaceutical and biotech companies can elevate laboratory compliance in 2026 through GLP, strategic outsourcing, and robust quality assurance.

Previous Post Arrow Next Post Arrow
ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero Targets

January 27, 2026

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero T...

ProPharma’s greenhouse gas reduction targets are validated by SBTi, aligning with the Net-Zero Standard and a commitment to reach net-zero by 2050.

ProPharma Expands Operations with New Office in Hyderabad

December 11, 2025

ProPharma Expands Operations with New Office in Hyderabad

ProPharma expands with a new office in Hyderabad, enhancing innovation and growth in regulatory, clinical, and compliance services for the life sciences industry.

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

December 4, 2025

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

ProPharma taps Daniel Ryan as President of Clinical Research Solutions, strengthening its clinical trial management leadership and expanding its FSP Solutions.

Previous Post Arrow Next Post Arrow
ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Previous Award Arrow Next Award Arrow
Case Study Setting up a Global PV System - ProPharma

Februar 5, 2026

Setting up a Global PV System

A company needed to rapidly establish a fully compliant global pharmacovigilance (PV) system, including UK/EU QPPV coverage, to meet regulatory requirements by a fixed deadline. With safety data and...

Case Study High-Volume Global Pharmacovigilance Onboarding - ProPharma

Januar 30, 2026

High-Volume Global Pharmacovigilance Onboarding

A global biotechnology sponsor faced a sudden surge in pharmacovigilance demand, with monthly ICSR volumes exceeding 30,000 cases across multiple regions. Limited internal capacity, tight onboarding...

Case Study Stabilizing High-Volume Legal Case Processing Through Structured Governance - ProPharma

Januar 28, 2026

Stabilizing High-Volume Legal Case Processing Through Structured Governance

ProPharma’s client faced escalating operational risk as high-volume legal case documentation overwhelmed their prior vendor. Thousands of documents, missed regulatory timelines, and a surge of...

Previous Resource Arrow Next Resource Arrow
Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

März 12, 2026

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

Uncover the intricacies of Pharmacovigilance System Master File (PSMF) management and explore proven strategies to ensure inspection readiness, effective MAH oversight, and regulatory compliance...

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

Februar 17, 2026

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

With promotional scrutiny increasing around areas such as social media, influencer campaigns, direct-to-consumer (DTC) messaging, and data-driven claims, the session walks through the characteristics...

Scaling High-Quality Medical Information Through Offshoring

Februar 11, 2026

Scaling High-Quality Medical Information Through Offshoring

Navigate the complexities of offshoring Medical Information and explore proven strategies to ensure consistent quality, regulatory compliance, and seamless global execution. Join us for an...

Previous Webinar Arrow Next Webinar Arrow

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