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Select any categories from those you have selected for your main listing. If you wish to include more categories, add them to your main listing first and after doing so, they will appear below.

Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

260

Analytical Methods Development

Clinical Research

157

Clinical Research Network Development

Clinical Trial Material Supply

Clinical Trials

110

Show More (4)

Document Management

Drug Product Manufacturing

Formulation Development

Submissions Management

Show Less (4)

Real World Data Research

Analytics Methods Development

Data Standardization & Curation

Evidence Prioritization

Late Phase Data Curation

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Observational Research

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129

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102

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117

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Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

260

Analytical Methods Development

Clinical Research

157

Clinical Research Network Development

Clinical Trial Material Supply

Clinical Trials

110

Show More (4)

Document Management

Drug Product Manufacturing

Formulation Development

Submissions Management

Show Less (4)

Real World Data Research

Analytics Methods Development

Data Standardization & Curation

Evidence Prioritization

Late Phase Data Curation

Lifecycle Evidence Generation

Show More (2)

Observational Research

Real World Evidence

Show Less (2)

Study Operations & Management

129

Patient Recruitment

Site Contracting & Payments

Site Identification & Activation

Site Relationship Management

Study Tracking & Analytics

Show More (1)

Trial Implementation

Show Less (1)

Trial Design & Planning

Data Management Planning

Enrollment Analytics

Patient Recruitment Planning

Protocol Feasibility Planning

Software

Show More (1)

Statistical Analysis Planning

Show Less (1)

Commercialization *

Brand Planning & Activation

Brand Vision & Positioning

Campaign Concept Testing

Multi-Channel Campaign Launch

Customer Engagement

Omnichannel Optimization

Patient Engagement

Patient Facing Solution Design

Patient Journey Analysis

Retention Program Effectiveness

Show More (1)

Strategic Account Management

Show Less (1)

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Billing & Reporting Operations

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Investment Performance Analytics

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Buy & Sell Side Advisory

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Market Access & Policy *

Global Market Access

Launch Sequencing

Payer Evidence Generation

Payer Relationship Management

Pricing Strategy

Reimbursement Consulting

Government Policy

Advocacy Management

Legislative Monitoring

Medical Affairs *

Defining the Value of Medical Affairs

Evidence Generation

102

Clinical Trial Concepts

Health Economics Modeling

Internal Medical Education

Patient Journey Mapping

Research Gap Analysis

Scientific Communications Development

Market Access Advisory Panels

Medical Writing

Payer Advisory Board Strategy

Strategic Communications Planning

Competitive Publications Analysis

Medical and Scientific Communications

Publication Planning

Scientific Platform Planning

Strategic Stakeholder Engagement

Advisory Board Strategy

KOL Relationship Management

Stakeholder Influence Mapping

Pharmacovigilance *

Risk Management

Risk Evaluation & Minimization

Risk Management Evaluation

Safety Communications

Safety Systems

Aggregate Reporting

Case Processing

Literature Searching

Safety Data Analytics

Safety Data Intake & Triage

Show More (3)

Safety Database Hosting

Safety Signal Evaluation

Signal Detection

Show Less (3)

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Facilities & Equipment

Calibration & PM Programs

Deviation Investigations

Equipment Maintenance

Facility Maintenance Programs

Facility Security Management

Production & Supply Chain

Clinical & Commercial Production

Labeling & Packaging

Storage & Distribution

Quality Management

Corrective Action Verification

Deviation Investigation

Quality Process Governance

Testing & Release

Batch Release Testing

Raw Material Testing

Stability Program Testing

Regulatory *

Compliance

185

Agency Meeting Support

Dossier & Application Development

eCTD Publishing & Validation

Pre-Submission Advisory Meetings

Regulatory Compliance

117

Show More (1)

Structured Content Authoring

Show Less (1)

Labeling & Promotions

Core Data Sheet Management

Labeling Strategy Development

Maintenance & Renewals

Post-Approval Safety Reporting

Promotional Material Compliance

Variations & Supplements

Transparency & Disclosure

Clinical Disclosure

Clinical Transparency

Technology & Operations *

Automation & Efficiency

Clinical Data Automation

Lab Automation Systems

Supply Chain Automation

Data & Analytics

146

Advanced Analytics

Artificial Intelligence

Data Curation

Data Visualization

Digital Health Solutions

100

5G Infrastructure

Blockchain Applications

mHealth Applications

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Telemedicine Platforms

Show More (1)

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Early Development

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345 California Street, Suite 325, San Francisco, CA 94104, USA

Paul Ehrlich Institute

Driving Innovation in Biomedicines

The Paul Ehrlich Institute is a federal agency that promotes research and testing to ensure the quality, efficacy and safety of biomedical drugs. Located in Langen, Germany, it has a long history dating back to 1896 and the pioneering work of Nobel laureate Paul Ehrlich.

With expertise spanning vaccines, blood products, gene therapies and more, the institute assesses new drug applications, monitors side effects and inspects manufacturing sites. It also operates its own labs to perform confirmatory testing. The Paul Ehrlich Institute works closely with European and global partners like the EMA and WHO to harmonize standards.

Through its research programs, it aims to advance regulatory science and the development of novel therapies for unmet needs. The institute is a go-to resource for industry and the medical community in Germany and beyond.

Driving Innovation in Biomedicines

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345 California Street, Suite 325, San Francisco, CA 94104, USA

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Paul Ehrlich Institute

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Paul Ehrlich Institute

Driving Innovation in Biomedicines

Driving Innovation in Biomedicines

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