Alhena Consult - Regulatory Affairs & Drug Development Email Formats

About Alhena Consult - Regulatory Affairs & Drug Development

Alhena Consult supports you throughout the development cycle of your products including project management, registration, pharmacovigilance and post MAA activities – whether you are a start-up or a large, established pharma company. We provide advice of the highest calibre along with enhanced operational support and our team works hand in glove with you – fully engaged until the successful completion of the project. Alhena's expertise includes the following areas: • Drug Development • European Regulatory Affairs • Project Management • Pharmacovigilance • Scientific writing Alhena’s team members have a distinct set of knowledge and experience in assisting start-ups and small and medium enterprises (SMEs), which needs are different than the ones of large pharmaceutical companies in terms of consultancy services and operational supports. In order to provide the best services possible, Alhena adapts its services to its clients’ needs and works with dedicated experts, as required by the projects. Both types of companies develop molecules, biologics from research to market. However, there is such a contrast in terms of manpower and R&D financial investments, and start-ups require a different level of care when it comes to risk assessment. Whereas SME will require more hands-on support on all aspects of development (strategy, operational supports …), a large pharmaceutical company will require more ad hoc help throughout periods of increased activity. All these types of services are provided by Alhena.

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