Using our years of experience in Product Development/Manufacturing/Project Management roles we can assist or autonomously conduct 'due diligence' activities to support your company’s expanding portfolio.
This can be applied to all dosage forms and all stages of development from candidate selection molecules through to compounds in Phase 3 clinical trials or even post-filing or post-registration products. Secure data storage can be provided as well as on-site review of data packages world-wide as required.
Due Diligence reports can be conducted as an independent third party reviewer or fully on behalf of a client brief. All work conducted under full client confidential disclosure agreements (CDAs) as required. Full reports can be issued detailing findings and if needed remedial plans and risk assessments.
Please contact us to discuss your specific requirements.