Product Development
Biotech & Pharmaceutical
Our expert teams are ready to support you through every step of the pharmaceutical product development process, leveraging our scientific, clinical and commercial expertise to help you maximize value at each stage.
Research & IP Evaluation Expertise
Our life science intellectual property practice provides analysis, assessment and strategic advice on life science IP. The practice is focused on both helping clients extract maximum value from their IP portfolios and supporting companies and investors conducting IP due diligence.
Cytopharma has considerable experience in working with academic research institutions and has worked with many universities, public- and third-sector research institutes, and research charities worldwide. We also undertake intellectual property due diligence on behalf of investor or acquirers, to support a transaction or asset…
Read moreContact us
Discuss our consulting services for the pharma & biotech industries with us.
Preclinical Strategy & Execution
Whether your product is a small molecule or biologic, Cytopharma can provide tailored assistance to help you plan and advance your program. This includes expertise in the complex CMC, safety and toxicology, and translational medicine aspects of today’s…
Read moreClinical Development
Our seasoned pharmaceutical physicians and functional specialists work to ensure that your program is on the optimal path foward, balancing risk and value, while responding to changes in the external environment. Cytopharma’s core team leverages 150+ industry-experienced, clinical development strategy and operations consultants, with backgrounds…
Read moreRegulatory Affairs
Our regulatory affairs consultants can help you devise effective regulatory strategies to place you on the best path torward regulatory approval, helping you avoid regulatory delays and overcome critical regulatory hurdles. We also provide hands-on support, including assistance with…
Read moreCMC Consulting
Whether you’re developing an oral small molecule, an autologous cell therapy, or anything in between, our CMC pharma experts can support your pipeline in the US and Europe. Each of our consultants brings significant industry experience and specialized knowledge across…
Read moreInterim Chief Medical Officer
Cytopharma has a number of CMO-level clinical MDs in our consulting group, who support our biotech clients as interim Chief Medical Officers, during for example, periods of extended search for a full-time individual. These scientific leaders are capable of overseeing flagship…
Read moreAbout our product development capabilities
From preclinical strategy to hands-on clinical development support, Cytopharma provides a range of product development services covering the full product life cycle. Our consultants average 20-30 years of industry experience, allowing them to draw on significant first-hand knowledge to help clients progress optimally, while navigating today’s increasingly competitive, complex and rapidly-changing drug development environment.
Our core team leverages our Expert Network, which contains over 150 expert product development consultants who specialize in specific technologies and disease areas, across the below functional disciplines:
- Oncology
- Biotechnology
- Biostatistics/Biometrics
- Chief Medical Officer
- Clinical Operations
- Clinical Quality Assurance
- Clinical Strategy/Oversight
- CMC-Manufacturing
- CMC-Regulatory/Quality
- Discovery-Biology
- eCTD-Regulatory Publishing
- Intellectual Property
- Medicinal Chemistry
- Medical/Technical Writing
- Pharm. Dev./Formulation
- Preclinical Pharmacology
- Project/Program Management
- Regulatory Affairs
- Supply Chain
- Toxicology/Safety Pharm.