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.
Increased Revenues
Optimized Organizational Operations:
years in Program and Project Management
Projects ≤ $10M USD Budget
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
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
View our services to see how RP3 can drive your projects to success?