Meet Our Experts

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                    Chemistry, Manufacturing and Control
                  
        Audit
Biopharmaceuticals
Cell Lines
CMO & CRO Selection and Management
Due Diligence
Formulation Development
GMP
Interim Management
In Vitro Diagnostics
IVD
Life-cycle Management
Program & Project Evaluation
Qualified Person
Quality Control and Assurance
R&D Strategies
Radiopharmaceuticals
Regulatory CMC
Risk Management
Scientific Writing

                    Non-clinical Research and Development
                  
        Contract Research Service
Disease Models
Drug Discovery
Due Diligence
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Interim Management
Oncology
Pharmacodynamics
Pharmacokinetics
Pharmacology
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R&D Strategies
REACH
Scientific Marketing
Scientific Writing
Target Identification
Test Laboratory Service
Toxicology

                    Clinical Development
                  
        Biomarkers
Biostatistics
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Clinical Development Phase II-III
Drug Safety
Due Diligence
In Vitro Diagnostics
IVD
Health Economics and Market Access
Imaging
Licensing
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Knowledge Management
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Medical Affairs
Medical Devices
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PK-PD
R&D Strategies
Submission Support
Translational Medicine

                    Regulatory Affairs and Compliance
                  
        Conformity Assessment
CTAs
Drug Safety
Due Diligence
In Vitro Diagnostics
IVD
GxPs
Life-cycle Management
Medical Devices
Pharmacovigilance
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Scientific Advice Procedures
SOPs
Submissions

                    Business Strategy & Development, Intellectual Property and Corporate Design
                  
        Agreements & Contracts
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Interim Management
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Experts for: Scientific Writing

Jörg TäubelExpert for cardiac safety in drug development
Hans HendriksExpert for Pre- and Early Clinical Drug Development
Scientific and Regulatory Medical Writing (Oncology, Inflammatory Diseases)
Non-Clinical and Early Clinical Anticancer Drug Development
Wolfgang M. RoßbergExpert for non-clinical drug safety and development