R & D

When we at partner 4 health enter in collaboration with Research & Development departments, we thrive to balance the rigorous work that a product development requires and the flexibility and pragmatism that our real world voices, building on the curiosity and the creativity that should characterize this segment in pharmaceutical and biotechnology companies. In addition, we enhance the awareness about other aspects that may affect the value of the product and how to handle them to bring the product to the patient. At the end of the day, what matters most is how the consumer, within his/her environment, could benefit from the developed product.

 

From the design of your development strategy to the reporting of study results, partner 4 health can support your R&D activities, especially through:

 

 

  • Portfolio evaluation, gap analysis & clinical development planning
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  • Experts’ interviews and contextual analysis of their feedback
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  • Investigators panel organization and coordination, expert report writing with meeting transcription and synthesis
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  • Clinical trial protocol and questionnaires conception, design, and writing prepared to ICH-GCP standards
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  • Clinical study reports (CSR) and integrated safety and efficacy summaries writing and editing (interim, final and abbreviated, according to ICH E3 format)
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  • Investigator brochures writing and editing with regular updates including safety reports
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  • Biostatistics support including meta-analysis of in-house data
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