About

Welcome to ZIMABio Consulting Solutions

At ZIMABio, we combine deep expertise with innovative solutions to redefine CMC consulting for biotech and pharmaceutical clients.

Our mission is to guide your therapies from discovery to regulatory approval, ensuring they reach patients in need. We provide a comprehensive suite of consulting services, supporting every stage of development—from preclinical and clinical phases to product approval and post-marketing strategies.

OUR SERVICES

Principal Consultant & Founder at ZIMABio Consulting Solutions LLC

Emina Osmancevic MSc.
Global Regulatory CMC Expert | Biotech & Pharma Operations Leader


With over 20 years in clinical, commercial, and biotechnology sectors, Emina Osmancevic is a strategic leader in regulatory CMC, specializing in product licensure, lifecycle management, and regulatory compliance for the pharmaceutical and biologics industries. Her extensive expertise includes oncology, immuno-oncology, gene therapy, and rare disease therapeutics, making her a sought-after leader & consultant for complex drug development and regulatory strategies. Known for a people-centric approach, Emina mentors cross-functional teams, fostering growth and collaboration to meet strategic regulatory milestones.


Emina has a Postgraduate degree in Chemistry Sciences, from the Syracuse University (2007) and a Bachelor of Science Degree in Chemistry, from the Utica College of Syracuse University, in New York State. 



www.linkedin.com/in/emina-osmancevic

https://www.linkedin.com/company/zimabio-cmc/


CONTACT US

Our Vision

Our vision is to be a trusted leader in biotech consulting, driving the transformation of innovative ideas into life-saving therapies. We strive to set new standards of excellence by empowering biotech pioneers to navigate the complexities of drug development with confidence and precision.

At ZimaBio, we are dedicated to providing exceptional consulting services tailored to the unique needs of biotech companies. With expertise in CMC consulting, clinical development, and regulatory affairs, we bridge the gap between groundbreaking science and the patients who need it most, creating a future where innovation leads to impactful health outcomes worldwide.

Our Mission

Our mission is to empower biotech innovators at every stage of the drug development journey, providing expert guidance and strategic solutions from initial discovery to regulatory approvals and beyond. With an unwavering commitment to excellence and precision, we help our clients navigate the complexities of product development, overcoming challenges in manufacturing, clinical advancement, and compliance with global regulatory standards.

We are dedicated to ensuring that groundbreaking therapies not only succeed in development but also reach the patients who need them most—safely, effectively, and efficiently. Through our collaborative approach, we work hand-in-hand with our partners to deliver tailored strategies that align with their goals while addressing the evolving demands of the healthcare landscape.

Our ultimate aim is to advance healthcare worldwide, enabling life-changing innovations to improve lives and create lasting, positive impacts on global well-being. At ZimaBio, we are driven by the belief that every therapy we help bring to market is a step closer to a healthier, more hopeful future.

Our Values

Our values define who we are and guide everything we do:

Integrity:  We uphold the highest ethical standards, ensuring transparency, accountability, and trust in every interaction.

Collaboration: We believe in the power of teamwork, fostering strong partnerships with our clients and within our organization to achieve shared goals.

Innovation:  We are committed to pushing boundaries, embracing creative solutions, and leveraging cutting-edge expertise to deliver exceptional outcomes.

These principles drive us to excel in our mission to support our partners and create meaningful impacts in the biotech and pharmaceutical industries.

Our commitment to these values guides every aspect of our work, fostering trust and collaboration with stakeholders across the entire spectrum of drug development—from early research and clinical trials to regulatory approvals and post-marketing support. These principles ensure we build strong, enduring partnerships while consistently delivering excellence at every stage of the process.

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