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J.K. Beugelink (MSc Pharm) has gained an extended experience in Regulatory Affairs. During a period of 30 years he has written more than 800 registration dossier parts, among which more than 500 expert reports.
He gained experience on Research Departments of a Contract Research Organization (CRO) and a pharmaceutical company. Moreover, J.K. Beugelink has been working as a Project Pharmacist on Manufacturing and Quality Assurance/Quality Control Departments of two bigger pharmaceutical companies. He has about 25 years of experience on Regulatory Affairs Departments of pharmaceutical companies, and more than 12 years as an entrepreneur.