Regulatory Affairs · Frankfurt / Rhine-Main · WRPA Bad Homburg
Regulatory Affairs Consultant for pharmaceutical companies in Frankfurt and Rhine-Main
Interim Regulatory Affairs Management and program leadership from a single source – with an office in Bad Homburg, 20 minutes from Frankfurt. On site with you in the region, remote for projects across DACH and the EU.
Why local?
Regulatory consulting with short distances.
Short distances
Workshops, kick-offs and stage-gate meetings on site in Frankfurt, Darmstadt, Wiesbaden, Mainz, Offenbach or the Taunus, without travel overhead.
Hybrid as needed
On site at the start and at critical milestones, remote in between.
German and English
Communication with BfArM and PEI in German, steering of international teams in English.
Services
What I take on for you.
Interim RA Management
Variations, renewals, PSUSA, authority liaison, dossier maintenance
Learn more → – Interim RA ManagementVariations & Lifecycle Management
Type IA, IB and II variations, renewals and lifecycle planning across products and markets.
Learn more → – Variations & Lifecycle ManagementeCTD v4.0 Project Coordination
Plan the move to eCTD v4.0, clarify requirements, manage tool vendor and timeline.
Learn more → – eCTD v4.0 Project CoordinationDiagnostic Sprint
Two weeks, fixed price EUR 5,000, up to 5 products and 3 markets
Learn more → – Diagnostic SprintProfile
Julius Vincenz Weidlich
Julius Vincenz Weidlich, Interim Regulatory Affairs & Program Manager. Over 20 years in the pharmaceutical industry, including 9 years of Regulatory Affairs in more than 100 markets and 8 years of project and program management (PMP). Based in Bad Homburg v.d.H.
Next step
A project in Frankfurt or Rhine-Main?
Tell me briefly about your project — or book a 30-minute call directly.