YOUR SATISFACTION IN ACHIEVING TECHNICAL & REGULATORY SUCCESS IS OUR PRIORITY
Helping companies help patients!
Engagement Flexibility
We recognize the global nature of drug development and are flexible to working with your colleagues in different geopgraphies/time zones.
Providing High Quality Services
We endeavor to provide quality and value in our engagements with customers.
Achieving Regulatory Milestones
We strive to help companies meet or exceed regulatory milestones.
Our promise
Committment
Fast, reliable
service
We are committed to provide quality services that are aligned with customer priorities and timelines.
Impact & Value
Expert
consulting
We will leverage our broad knowledge of the drug development and regulatory approval process to bring impact and value to customer projects.
Our team
Our team of consultants has 75+ years of experience in the Pharmaceutical Industry.
Jadwiga Martynowicz, DM, MS
Consultant
With over 30 years of experience in pharmaceutical regulatory affairs, Jadwiga can help you develop global regulatory strategies, provide input into design of clinical trials, prepare for meetings with health authorities, and prepare high quality marketing authoriization applications.
Robert Jerzewski, PhD
Consultant
With over 40 years of Pharmaceutical Industry experience and 8 NDAs, Bob can help you with formulation & process development, technology transfer, outsourcing network management, alliance management and strategy development engagements.
Contact us
Telephone: +1 908 281 0645
E-mail: mailto:robert.jerzewski@neokee-pharma.com
Address: 162 North Street, Belle Mead, NJ 08502 USA
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