Social Media Monitoring und Social Response Management

Umfassende Lösungen für regulatorische Anforderungen im Bereich Social Media.

Erfahrungen und Kompetenzen im Bereich Community Management

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Maßgeschneiderte Community-Management-Services

Dienstleistungen, die individuell auf Ihre Bedürfnisse zugeschnitten sind.

Maßgeschneiderte Community-Management-Services

Dienstleistungen, die individuell auf Ihre Bedürfnisse zugeschnitten sind.

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Multilinguale Services

35+ Sprachen

Multilinguale Services

35+ Sprachen

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Hochqualifizierte Expert*innen

Unser Team ist auf AE‑ und PQC‑Berichterstattung spezialisiert und steht für exzellenten Service.

Hochqualifizierte Expert*innen

Unser Team ist auf AE‑ und PQC‑Berichterstattung spezialisiert und steht für exzellenten Service.

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Globales Serviceangebot

Wir bieten Erfahrungen mit Community-Management-Services auf der ganzen Welt unter Einhaltung der Vorschriften verschiedener Aufsichtsbehörden.

Globales Serviceangebot

Wir bieten Erfahrungen mit Community-Management-Services auf der ganzen Welt unter Einhaltung der Vorschriften verschiedener Aufsichtsbehörden.

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Kompetenzen mit verschiedenen Plattformen

Facebook, Instagram, LinkedIn, X und mehr.

Kompetenzen mit verschiedenen Plattformen

Facebook, Instagram, LinkedIn, X und mehr.

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Social Media Monitoring Services

ProPharma überwacht sorgfältig die Social-Media-Kanäle unserer Kund*innen und achtet dabei auf auftretende unerwünschte Ereignisse oder Produktbeschwerden. Sobald wir etwas Meldepflichtiges entdecken, dokumentieren wir es umgehend und melden es innerhalb der vorgeschriebenen Frist, um sicherzustellen, dass keine wichtigen Informationen verloren gehen.

Social Response Management

ProPharma geht aktiv auf Kommentare und Anfragen von Verbrauchern auf verschiedenen Social-Media-Plattformen ein und agiert dabei in Ihrem Namen. Wir verwenden von Kund*innen genehmigte standardisierte Antworten, die speziell auf diese Interaktionen zugeschnitten sind. Ob wir öffentlich auf Kommentare unter Beiträgen oder privat über Direktnachrichten antworten, ProPharma stellt sicher, dass jede Interaktion professionell, angemessen und nicht werblich ist. Mit diesem Service entfernt ProPharma auch unangemessene Kommentare aus Ihren Beiträgen, um das professionelle Image Ihres Unternehmens zu wahren.

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Kontaktieren Sie uns zu unserer Expertise im Bereich Community-Management Service

Wir haben es uns zur Aufgabe gemacht, die Gesundheit und das Wohlbefinden der Verbraucherinnen durch umfassendes Community-Management zu verbessern. Ganz gleich, ob Sie zuverlässige Social-Media-Monitoring-Dienstleistungen oder einen Komplettservice einschließlich Social Response Management benötigen, unser Expert*innenteam steht Ihnen gerne zur Verfügung.

News & Insights

From Feasibility to First Patient In: Streamlining Study Start‑Up with Confidence

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From Feasibility to First Patient In: Streamlining Study Start‑Up with Confidenc...

Discover how ProPharma streamlines clinical trial study start-up, ensuring predictable activation and reducing risks from feasibility to first patient in.cl

QMSR Explained: Key Changes from FDA QSR to the New Quality Management System Regulation

Juli 23, 2026

QMSR Explained: Key Changes from FDA QSR to the New Quality Management System Re...

The FDA's transition to the QMSR simplifies compliance, emphasizing risk management and aligning with global standards for medical devices compared to QMR.

Building Relationships with Sites: The Hidden Driver of Faster Start-Ups

Juli 20, 2026

Building Relationships with Sites: The Hidden Driver of Faster Start-Ups

Discover effective strategies for building relationships with clinical trial sites to streamline the study start-up process and enhance activation timelines.

ProPharma Advances Technology Enablement Strategy with AI-Assisted Capability for ANDA Submission Development

Juli 8, 2026

ProPharma Advances Technology Enablement Strategy with AI-Assisted Capability fo...

ProPharma unveils an AI-assisted capability to enhance ANDA submission development, improving efficiency and maintaining regulatory excellence for clients.

ProPharma Welcomes Kevin van Dooren to Strengthen Integrated EU Regulatory and HTA Capabilities

Juni 18, 2026

ProPharma Welcomes Kevin van Dooren to Strengthen Integrated EU Regulatory and H...

ProPharma welcomes Kevin van Dooren as Vice President, HEOR and Market Access, strengthening integrated EU regulatory, HTA, reimbursement, and market access capabilities for life sciences companies.

ProPharma Appoints Adrian Pencak as Chief Commercial Officer

Mai 27, 2026

ProPharma Appoints Adrian Pencak as Chief Commercial Officer

ProPharma announces Adrian Pencak as Chief Commercial Officer, bringing 25 years of leadership experience to enhance global commercial capabilities and client partnerships.

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 Inspection-Ready AI: Building Quality Frameworks That Keep Pace with Innovation - ProPharma

Juli 23, 2026

Inspection-Ready AI: Building Quality Frameworks That Keep Pace with Innovation

As artificial intelligence becomes increasingly embedded across life sciences, organizations face a growing challenge: ensuring quality and compliance frameworks evolve alongside rapidly advancing...

Case Study Ensuring Continuity of Neonatal Vitamin Prophylaxis During a Product Shortage: A Regulatory and Pharmacovigilance-Led Solution - ProPharma

Juli 15, 2026

Ensuring Continuity of Neonatal Vitamin Prophylaxis During a Product Shortage: A...

Product shortages involving essential medicines can create significant clinical and regulatory challenges, particularly when vulnerable patient populations depend on uninterrupted access to...

Case Study Meeting Patients Where They Are: Delivering Global Clinical Support for Time-Sensitive Research - ProPharma

Juni 17, 2026

Meeting Patients Where They Are: Delivering Global Clinical Support for Time-Sen...

Conducting clinical research for rare pediatric populations presents unique operational challenges, particularly when eligible patients may be born anywhere in the world and require immediate...

From Feasibility to First Patient In: How to Streamline Study Start-Up  

September 30, 2026

From Feasibility to First Patient In: How to Streamline Study Start-Up  

Clinical trial delays often begin long before study conduct, with critical decisions made during feasibility and study start-up shaping the success of the entire trial. Join this webinar to discover...

Tech Meets Touch: Evaluating Empathy and AI in Medical Information Delivery

Juni 4, 2026

Tech Meets Touch: Evaluating Empathy and AI in Medical Information Delivery

Artificial intelligence (AI) is a hot topic in Medical Information (MI), yet real-world evidence of its impact in regulated, human-led MI environments remains limited. Hear practical, evidence-based...

Foundations of a Compliant EU–UK GMP–GDP Supply Chain: From Importation to Distribution

Juni 2, 2026

Foundations of a Compliant EU–UK GMP–GDP Supply Chain: From Importation to Distribution

A compliant and efficient EU–UK GMP–GDP supply chain requires a clear understanding of roles, responsibilities, and operational integration across importation, certification, and distribution...

News & Insights

From Feasibility to First Patient In: Streamlining Study Start‑Up with Confidence

July 27, 2026

From Feasibility to First Patient In: Streamlining Study Start‑Up with Confidenc...

Discover how ProPharma streamlines clinical trial study start-up, ensuring predictable activation and reducing risks from feasibility to first patient in.cl

QMSR Explained: Key Changes from FDA QSR to the New Quality Management System Regulation

July 23, 2026

QMSR Explained: Key Changes from FDA QSR to the New Quality Management System Re...

The FDA's transition to the QMSR simplifies compliance, emphasizing risk management and aligning with global standards for medical devices compared to QMR.

Building Relationships with Sites: The Hidden Driver of Faster Start-Ups

July 20, 2026

Building Relationships with Sites: The Hidden Driver of Faster Start-Ups

Discover effective strategies for building relationships with clinical trial sites to streamline the study start-up process and enhance activation timelines.

Previous Post Arrow Next Post Arrow
ProPharma Advances Technology Enablement Strategy with AI-Assisted Capability for ANDA Submission Development

July 8, 2026

ProPharma Advances Technology Enablement Strategy with AI-Assisted Capability fo...

ProPharma unveils an AI-assisted capability to enhance ANDA submission development, improving efficiency and maintaining regulatory excellence for clients.

ProPharma Welcomes Kevin van Dooren to Strengthen Integrated EU Regulatory and HTA Capabilities

June 18, 2026

ProPharma Welcomes Kevin van Dooren to Strengthen Integrated EU Regulatory and H...

ProPharma welcomes Kevin van Dooren as Vice President, HEOR and Market Access, strengthening integrated EU regulatory, HTA, reimbursement, and market access capabilities for life sciences companies.

ProPharma Appoints Adrian Pencak as Chief Commercial Officer

May 27, 2026

ProPharma Appoints Adrian Pencak as Chief Commercial Officer

ProPharma announces Adrian Pencak as Chief Commercial Officer, bringing 25 years of leadership experience to enhance global commercial capabilities and client partnerships.

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 Inspection-Ready AI: Building Quality Frameworks That Keep Pace with Innovation - ProPharma

Juli 23, 2026

Inspection-Ready AI: Building Quality Frameworks That Keep Pace with Innovation

As artificial intelligence becomes increasingly embedded across life sciences, organizations face a growing challenge: ensuring quality and compliance frameworks evolve alongside rapidly advancing...

Case Study Ensuring Continuity of Neonatal Vitamin Prophylaxis During a Product Shortage: A Regulatory and Pharmacovigilance-Led Solution - ProPharma

Juli 15, 2026

Ensuring Continuity of Neonatal Vitamin Prophylaxis During a Product Shortage: A...

Product shortages involving essential medicines can create significant clinical and regulatory challenges, particularly when vulnerable patient populations depend on uninterrupted access to...

Case Study Meeting Patients Where They Are: Delivering Global Clinical Support for Time-Sensitive Research - ProPharma

Juni 17, 2026

Meeting Patients Where They Are: Delivering Global Clinical Support for Time-Sen...

Conducting clinical research for rare pediatric populations presents unique operational challenges, particularly when eligible patients may be born anywhere in the world and require immediate...

Previous Resource Arrow Next Resource Arrow
From Feasibility to First Patient In: How to Streamline Study Start-Up  

September 30, 2026

From Feasibility to First Patient In: How to Streamline Study Start-Up  

Clinical trial delays often begin long before study conduct, with critical decisions made during feasibility and study start-up shaping the success of the entire trial. Join this webinar to discover...

Tech Meets Touch: Evaluating Empathy and AI in Medical Information Delivery

Juni 4, 2026

Tech Meets Touch: Evaluating Empathy and AI in Medical Information Delivery

Artificial intelligence (AI) is a hot topic in Medical Information (MI), yet real-world evidence of its impact in regulated, human-led MI environments remains limited. Hear practical, evidence-based...

Foundations of a Compliant EU–UK GMP–GDP Supply Chain: From Importation to Distribution

Juni 2, 2026

Foundations of a Compliant EU–UK GMP–GDP Supply Chain: From Importation to Distribution

A compliant and efficient EU–UK GMP–GDP supply chain requires a clear understanding of roles, responsibilities, and operational integration across importation, certification, and distribution...

Previous Webinar Arrow Next Webinar Arrow