Our lead consultant, Patrick, has over a decade of experience working with biotechnnology and pharmacaeutical companies of all types. From early stages of drug discovery, through regulatory approval and all stages of clinical phases, KendallPharma have provided clients with:

• Long-term project oversight and management.
• Clinical strategy planning consultancy.
• CRO/CDMO partner liaison and management.
• Clinical research lead and guidance, including pre-clinical and clinical study design and oversight.
• Advice and consulting input and report generation in a broad range of therapeutic areas.

KendallPharma offers include generation of comprehensive range of clinical and scientific documentation generation, including:
• Gap analysis reports
• TPP analysis and competitor profiling.
• Pre-clinical and clinical stage study protocol design.
• Clinical research development planning.
• Therapeutic target analysis and review.
• Scientific writing inc. Journal articles and systematic reviews.
• Press and promotional material.

Working to suit clients in full-time, contracting or consultancy capacities, Patrick’s strong experience and knowledge, communication skills and clear decision-making are here to support you.

We have the experience and expertise to support our clients whatever their clinical and scientific needs. To talk with us about your project or requirements, please do not hesitate to contact us via email: kendallpharma@gmail.com or with the contact form on this site.