Project Management - Development teams
We offer you a wide range of services, from coordinating an individual trial up to coordination of a development program.
Welcome
DGr Pharma provides expert drug development consultancy, supporting biotech and pharmaceutical companies in navigating complex development pathways with confidence.
Working in close collaboration with preclinical and clinical R&D teams, we deliver strategic guidance and hands-on support across nonclinical, clinical, and CMC development — from early discovery through to IND/CTA submission.
Our team combines deep industry and regulatory expertise, helping to guide decision-making, optimise development plans, support execution, and mitigate risk at every stage of the programme.
Our services
Non-clinical development
We can assist you with the operational aspects of your project and help you to define the non-clinical development program …
Clinical development - consultancy
We can assist you with the operational aspects of your project and help you to define your clinical development strategy…
Pharmacokinetics - Data analysis
We have a strong history of analyzing drug concentration-time data that derive from all stages of drug development studies…
Chemistry, Manufacturing & Control (CMC)
DGr Pharma’s department of Chemistry, Manufacturing & Control (CMC) can assist you with an extensive range of activities …
Regulatory affairs
DGr Pharma provides expert opinions on regulatory-related questions and procedures and liaises to regulatory authorities.
Quality
The Quality Assurance Unit (QUA) at DGr Pharma is responsible for the Quality Management System, which is based on the OECD Guidelines of Good Laboratory Practice (GLP).
IT and Data Storage
Integrity and security of records and data is essential throughout the product life cycle of any pharmaceutical company from R&D up to marketing.
Latest news
DGr Pharma is hiring a Document Manager, (e-)Archivist and Personnel File Administrator
DGr Pharma is looking for a highly organised and detail-oriented Document Manager, (e-)Archivist and Personnel File Administrator to join our team in Breda, the Netherlands. This part-time, office-based position (16 hours per week) plays an important role in supporting document management, physical and electronic archiving, personnel file administration, and office coordination. Working within a GLP-regulated […]
Open position for a Senior Consultant Clinical Pharmacology and Pharmacokinetics
We are looking for a Senior Consultant Clinical Pharmacology and Pharmacokinetics to join our team. If you are interested, please visit LinkedIn