Pharmaceutical & BioTech

Our services along the whole product lifecycle
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Discover all our Pharmaceutical & BioTech services

Drug Development Regulatory Affairs Market Access Pharmacovigilance Quality & Compliance Case Studies

Drug Development

Drug Development Strategy Gap Analysis SME Status Orphan Drug Designation (ODD) Scientific Advice Pediatric Investigation Plan (PIP) PRIME (PRIority MEdicines) scheme CMC Regulatory solutions Clinical Trial Application (CTA) Due Diligence

Regulatory Affairs

Registration Strategy Marketing Authorization Application (MAA) CMC Regulatory solutions Dossier Development Life cycle management Due Diligence Launch readiness Advertising & Promotion

Market Access

Early Access Programs Market Access Strategy Pricing & Reimbursement Dossier Health Economic Models Negotiation with Health Authorities Pricing & Reimbursement maintenance Joint Clinical Assessment (JCA) Integrated strategy and execution in the European markets

Pharmacovigilance

QPPV Services EudraVigilance services Pharmacovigilance System Master File (PSMF) Local Pharmacovigilance

Quality & Compliance

Quality & Compliance

Case studies

Every client is unique.
Every healthcare product is unique.
But some regulatory challenges are common.


RPN can provide you with tailored solutions to effectively achieve your objectives.

Due Diligence for Acquisition

Regulatory Pathway for ATMP

Local Comprehensive Support

A Global RA Function

Accelerating ODD and Approval

Streamlining Global Compliance

EU Presence for US company

Global Life-Cycle Management

Navigating NCE Development

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