We deliver on your promises
Whether a pharmaceutical, biotech or medical device company, we are your ideal mid-sized, full-service CRO.
Our in-depth expertise and long lasting experience combined with a flexible, and collaborative approach allow us to tailor our responses to each individual study.
Our clinical development capabilities span through trial Phases I-IV, across a broad range of therapeutic areas including medical devices.
We have an excellent track record for supporting a range of stakeholders in the pharmaceutical industry including sponsors and research institutions at each clinical development phase.
1700
completed
projects
85
repeat
business
88
positive
recommendation
8
site inspections
from EMA/FDA completed
Tailor-made solutions
Your effective and rigorously compliant project strategy will be tailor-made to the specific requirements of your clinical trial. Our flexibility in project design and implementation, based on our in-house expertise and experience is backed up by delivering full-service with deep expertise.
Your Regulatory and Operational Local Expert
Our highly experienced local regulatory and operational experts located in 40 countries throughout Europe and North America to support any strategic questions to optimize your design and the delivery of your project.
Delivery focused
A proud track record of accelerated start-up timelines, over-achievement of recruitment targets, early completions and cost competitive budgetary adherence demonstrates that we are extremely focused at running efficient and effective clinical trials.
Shared goals
You need a CRO partner who is as invested in the success of each bespoke clinical trial as you are. We collaborate closely, constantly making sure that we are aligned with your study expectations and key study milestones. Essentially, we become an extended arm to your team with the same shared goals.
Pharmaceutical companies
Delivery-focused bespoke solutions for all phases of drug development.
Biotechnology enterprises
Dedicated service and expertise that delivers high-quality, cost-effective results.
Medical Device companies
Smart solutions built on a combination of regulatory expertise and deep understanding of project specificities.
News
CTIS: First Optimapharm Experiences, an Interview with Sara Weytjens
CTIS – First Optimapharm Experiences, an Interview with Sara Weytjens In recent years, CTIS has become a major topic of discussion in the field of EU clinical research. The implementation of this system has completely transformed traditional practices and had…
Read More Optimapharm announces Jelena Pavlović as Senior Director, Trial Support
Optimapharm announces Jelena Pavlović as Senior Director, Trial Support Optimapharm, a leading, mid-sized, full-service CRO across Europe and North America, is excited to announce the appointment of Jelena Pavlović as Senior Director, Trial Support, effective August 2023 "It is such…
Read More Optimapharm announces Sara Weytjens as Vice President, Regulatory and Site Activation
Optimapharm announces Sara Weytjens as Vice President, Regulatory and Site Activation Optimapharm, a leading, mid-sized, full-service CRO across Europe and North America, is excited to announce the appointment of Sara Weytjens as Vice President, Regulatory and Site Activation, effective April…
Read More Optimapharm confirms Mirna Šenjug Novak as Group CFO
Optimapharm confirms Mirna Šenjug Novak as Group CFO Optimapharm, a leading, mid-sized, full-service CRO (Contract Research Organization) across Europe and North America, is excited to announce the promotion of Mirna Šenjug Novak as Group Chief Financial Officer (CFO), effective February…
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