Program and Project Management Consulting in Drug Development

Empowering Your Organization Throughout the Drug Development Journey:
From Defining Strategy to Achieving Success

About Us

     RP3 Management Consulting Inc. is committed to enabling the biotechnology and pharmaceutical industries to transform the quality of life for patients worldwide. We do this by guiding teams through meaningful change, culminating in the achievement of the organization’s critical goals.

Our mission is to leverage our unique blend of knowledge and real-world experience to deliver exceptional fractional Program and Project Management, as well as change management leadership consulting services; so our clients can successfully navigate the complexities of drug development and commercialization.

From start-ups to established companies, from early in vivo/in vitro preclinical to IND studies and through to pivotal clinical study read-outs, RP3 aligns, directs, and secures project stakeholder commitment to deliver successful project outcomes across the spectrum of preclinical, manufacturing, regulatory and clinical development activities, and market introduction.

RP3 will Guide, Orchestrate and Deliver your strategic initiatives.

Why choose RP3?

1- Proven Track Record of Business Success

Increased Revenues

Optimized Organizational Operations:

Proven Track Record of Business Success

2- Extensive Industry Experience

0 +
years in Drug Development
0 +

years in Program and Project Management

0 +

Projects ≤ $10M USD Budget

Examples of Project/Activity Oversight
project-activity Drug Development Program

Innovators

Generics

Pre-IND/CTA

Submission

Health Authority Requests

Marketing Authorization

Physicochemical Properties

Formulation & Analytical Development

Clinical Trial Material

Registration

Engineering Validation/Commercial

Phase 1

Phase 2

Phase 3 (single site)

In vitro & In vivo ADME

Safety Pharmacology

Toxicology

Carcinogenicity

DRF studies

PK

project-activity Drug Development Program

Innovators

Generics

Pre-IND/CTA

Submission

Health Authority Requests

Marketing Authorization

Physicochemical Properties

Formulation & Analytical
Development

Clinical Trial Material

Registration

Engineering
Validation/Commercial

Phase 1

Phase 2

Phase 3
(single site)

In vitro & In vivo
ADME

Safety
Pharmacology

Toxicology

Carcinogenicity

DRF studies

PK

3- Highest Standard Qualifications
We bring the highest level of expertise to every project. With proven experience and qualifications in project management and change management, we deliver results through a disciplined, structured approach that meets industry best practices. Trust us to provide the strategic guidance and operational excellence you need to drive successful outcomes.
certified desktop
Our principles
icon guide - Project Management Consulting
Guide
We offer expert fractional program and project management, as well as change management leadership to help your team navigate the complexities of drug development and commercialization, with clarity and purpose.
icon orchestrate -Project Management Consulting
Orchestrate
We align people, processes, and resources to drive your strategic initiatives forward, ensuring seamless collaboration and keeping projects on track for success.
icon deliver - Project Management Consulting
Deliver
We are committed to delivering results that make a lasting impact. From preclinical research through clinical trials, regulatory approvals and market introduction, we ensure your projects achieve successful outcomes that positively impact patients worldwide.

View our services to see how RP3 can drive your projects to success?

Merci

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