Services
The services Dekking Consultancy can provide include, but are not limited to:
- Advice and hands-on support in the field of Project Management for development of pharmaceutical products in preclinical early research & development phase.
- Execution of outsourced studies especially for analytical- and preclinical studies according to GCP principles including,
- Development of Study design
- Selection of the right Contract Research Organization (CRO) or External Service Provider (ESP)
- Support of Contract Negotiations
- Supervising the drafting of a Quality Agreement
- Study Execution including study oversight services: quality compliance monitoring, progress and result monitoring, data integrity checks
- Reporting
- Selection of the right service provider for your “Proof of Concept” studies of pharmaceutical products in Early Research and Development phase (preclinical studies and sample analysis) considering: Knowledge
Capability, Quality, Price (competitive bid), Capacity
- Scientific Writing Support
- e.g.: Writing of Project licenses for the Dutch “Centrale Commissie Dierproeven” (CCD) for execution of animal studies within The Netherlands.
- e.g.: Writing of Project licenses for the Dutch “Centrale Commissie Dierproeven” (CCD) for execution of animal studies within The Netherlands.
- Trainings for conducting scientific studies at a high-quality level (GCP compliant)
If, based on my experience and CV, you have another question or assignment, please feel free to contact me so we can discuss possibilities.
