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Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

204

Analytical Methods Development

Clinical Research

120

Clinical Research Network Development

Clinical Trial Material Supply

Clinical Trials

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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113

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Defining the Value of Medical Affairs

Evidence Generation

101

Clinical Trial Concepts

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Internal Medical Education

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Research Gap Analysis

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Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

204

Analytical Methods Development

Clinical Research

120

Clinical Research Network Development

Clinical Trial Material Supply

Clinical Trials

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 (1)

Observational Research

Show Less (1)

Study Operations & Management

113

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

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Statistical Analysis Planning

Show Less (1)

Commercialization *

Brand Planning & Activation

Brand Vision & Positioning

Campaign Concept Testing

Multi-Channel Campaign Launch

Customer Engagement

Omnichannel Optimization

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Patient Facing Solution Design

Patient Journey Analysis

Retention Program Effectiveness

Show More (1)

Strategic Account Management

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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

101

Clinical Trial Concepts

Health Economics Modeling

Internal Medical Education

Patient Journey Mapping

Research Gap Analysis

Scientific Communications Development

Market Access Advisory Panels

Payer Advisory Board Strategy

Strategic Communications Planning

Competitive Publications Analysis

Publication Planning

Scientific Platform Planning

Strategic Stakeholder Engagement

Advisory Board Strategy

KOL Relationship Management

Stakeholder Influence Mapping

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Risk Evaluation & Minimization

Risk Management Evaluation

Safety Communications

Safety Systems

Safety Data Analytics

Safety Data Intake & Triage

Safety Signal Evaluation

Quality & Mfg *

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Calibration & PM Programs

Deviation Investigations

Equipment Maintenance

Facility Maintenance Programs

Facility Security Management

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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

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Compliance

153

Agency Meeting Support

Dossier & Application Development

eCTD Publishing & Validation

Pre-Submission Advisory Meetings

Regulatory Compliance

Labeling & Promotions

Core Data Sheet Management

Labeling Strategy Development

Maintenance & Renewals

Post-Approval Safety Reporting

Promotional Material Compliance

Variations & Supplements

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Clinical Disclosure

Clinical Transparency

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Clinical Data Automation

Lab Automation Systems

Supply Chain Automation

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Advanced Analytics

Artificial Intelligence

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Telemedicine Platforms

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Early Development

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About

Evidence Generation

Research Gap Analysis

Pharmacovigilance

Safety Systems

Safety Data Analytics

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Headquarters

265 Franklin Street, Suite 1101, Boston, MA 02110, USA

biologit

Transform Your Literature Monitoring with AI-Powered Efficiency

biologit offers a comprehensive SaaS platform for automated literature screening and safety surveillance. Powered by AI, their solution delivers up to 70% productivity gains for pharmacovigilance teams. With configurable workflows, integrated search across global and regional sources, and automatic de-duplication, biologit streamlines safety screening for drugs, devices, cosmetics and more. Hosted on secure EU data centers, the platform is validated, GxP-ready and CFR-11 compliant.

Their consultancy services provide qualified support including EU QPPV and RPPV roles. With expertise across human, veterinary and medical device safety, biologit enables sponsors, MAHs and applicants to implement robust pharmacovigilance programs.

Transform Your Literature Monitoring with AI-Powered Efficiency

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