Meet Our Experts

Please select a topic:

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

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

                    Clinical Development
                  
        Biomarkers
Biostatistics
Business Development
Clinical Development Phase I
Clinical Development Phase II-III
Drug Safety
Due Diligence
Health Economics and Market Access
Imaging
Licensing
Interim Management
Knowledge Management
Life-cycle Management
Medical Affairs
Medical Devices
Pharmacogenetics
PK-PD
R&D Strategies
Submission Support
Translational Medicine

                    Regulatory Affairs and Compliance
                  
        Conformity Assessment
CTAs
Drug Safety
Due Diligence
GxPs
Life-cycle Management
Medical Devices
Pharmacovigilance
Quality Assurance
Quality Systems
Regulatory Affairs
Regulatory Databases
Regulatory Strategies
Scientific Advice Procedures
SOPs
Submissions

                    Business Strategy & Development, Intellectual Property and Corporate Design
                  
        Agreements & Contracts
Business Development
Business Representation
Commercial Strategy
Commercial Operations
Communication
Corporate Design
Corporate Finance
Funding Opportunities
General Management
Intellectual Property
Interim Management
Law
Licensing
M&As
Market Research
Marketing
Sales
Social Media
Trademarks

Experts for: Preclinical Development

Michael HildebrandExpert 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 HendriksExpert for Pre- and Early Clinical Drug Development
Non- and Early Clinical Anticancer Drug Development
Scientific and Medical Writing
Charlie BrindleyExpert for Pre-clinical and Clinical Pharmacokinetics
PK-PD modelling
Allometric scaling from animals to man
GLP and GCP Report Writing
Matthias BräutigamExpert for drug research and preclinical development
Imaging agents
Imaging technologies
Medicated devices
Jens HoffmannExpert for Research and Drug Discovery in Oncology
Validation and characterization of oncology targets
Tumor models, stem cells
Biomarker identification, translational research
Frank S. ZollmannExpert for Pre-/ Clinical Drug Development
Safety pharmacology, toxicology, pharmacogenomics
Integrated preclinical & clinical development up to PoC
Clinical pharmacology
Pascal PillerExpert for Project Management and Contract Research
Full range Test Laboratory Service for REACH/Preclinic
Regulatory Affairs Service / Material Safety Data Sheets
Product safety-tests, in-vitro tests and SVHC analyses
Jürgen ConradExpert for public funding of R&D
Identification of European funding opportunities
Planning of R&D projects according the funding rules
Coordinating of contract negotiations
Project management of funded projects
Wolfgang M. RoßbergExpert for non-clinical drug safety and development
Investigative toxicology
Regulatory toxicology
Evaluation of in-/out-licensing candidates