Meet Our Experts

Please select a topic:

                     
                    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
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                    Non-clinical Research and Development
                  
        Contract Research Service
Disease Models
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Due Diligence
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Interim Management
Oncology
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Pharmacokinetics
Pharmacology
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R&D Strategies
REACH
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Toxicology

                    Clinical Development
                  
        Biomarkers
Biostatistics
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Clinical Development Phase I
Clinical Development Phase II-III
Clinical Operations
Clinical Study Management
Drug Safety
Due Diligence
In Vitro Diagnostics
IVD
Health Economics and Market Access
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Interim Management
Knowledge Management
Life-cycle Management
Medical Affairs
Medical Devices
Pharmacogenetics
PK-PD
Quality Risk Management
R&D Strategies
Submission Support
Translational Medicine
Vendor management
Vendor selection

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

                    Business Strategy & Development, Intellectual Property and Corporate Design
                  
        Agreements & Contracts
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Interim Management
Law
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Social Media
Trademarks

Experts for: Interim Management

Michael Hildebrand

Expert for CMC, Biopharmaceuticals and QP topics

CMC support from research to life cycle management
Formulation development and Quality Control
GMP and Qualified Person support

Hans Hendriks

Expert for Pre- and Early Clinical Drug Development

Scientific and Regulatory Medical Writing (Oncology, Inflammatory Diseases)
Non-Clinical and Early Clinical Anticancer Drug Development