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
Scientific Writing

                    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
In Vitro Diagnostics
IVD
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
In Vitro Diagnostics
IVD
GxPs
Life-cycle Management
Medical Devices
Pharmacovigilance
Quality Assurance
Quality Systems
Regulatory Affairs
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: GxPs

Siglinde Dürr

Expert for Quality Assurance

Implementation of Quality Systems according to GMP, GCP or ISO regulations
Conduct quality audits (GMP/GCP/ISO)
Develop and implement Standard Operating Procedures
Project management of funded projects

Pascal Piller

Expert 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