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Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

206

Analytical Methods Development

Clinical Research

121

Clinical Research Network Development

Clinical Trial Material Supply

Clinical Trials

Show More (4)

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Drug Product Manufacturing

Formulation Development

Submissions Management

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Defining the Value of Medical Affairs

Evidence Generation

101

Clinical Trial Concepts

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Early Development

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Clinical Research *

Clinical Reporting

Abstract & Poster Development

Clinical Study Report Writing

Manuscript Development

Product Development

206

Analytical Methods Development

Clinical Research

121

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

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

Internal Audit Support

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

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 *

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

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

Transparency & Disclosure

Clinical Disclosure

Clinical Transparency

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Clinical Data Automation

Lab Automation Systems

Supply Chain Automation

Data & Analytics

Advanced Analytics

Artificial Intelligence

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Telemedicine Platforms

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Early Development

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About

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101 East River Drive, E Hartford, CT 06108, USA

Novotech

Accelerating Clinical Trials in Asia Pacific

Novotech is a leading Asia-Pacific CRO providing clinical development services across all phases of drug development. With extensive operations across APAC and the US, Novotech offers deep regional expertise combined with operational excellence. Novotech accelerates clinical trials through faster patient recruitment and high-quality data. Key therapeutic areas include oncology, infectious diseases, liver disease, and rare diseases.

Novotech leverages strong relationships with medical institutions, regulators, and KOLs throughout APAC to ensure efficient study start-up and successful study completion. The CRO offers a full range of services including medical and regulatory consulting, data management, biometrics, pharmacovigilance, and more. Novotech has a team of over 2500 professionals across 45 offices in 16 countries.

Accelerating Clinical Trials in Asia Pacific

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Novotech

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Accelerating Clinical Trials in Asia Pacific

Accelerating Clinical Trials in Asia Pacific

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