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: GxPs

Mónica Unger-BadyExpert for Regulatory Compliance in Pharmaceutical Industry
Analysis, individual consultation, implementation
Project management, interim management
Business analysis
Coaching and Training
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
Siglinde DürrExpert 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