Where we are
Our main offices are located in Cyprus (EU), we also have ClinBAY teams located in Europe, South America, and Indian Ocean.
We have customers located worlwide across the healthcare industry.
Our Customers
Our customers are located worldwide across the healthcare industry:
- Major Pharmaceutical - Strategic Partner to 2 Major Pharma’s
- Biopharmaceutical - Several Partners worldwide
- Cosmetic - One of largest in the industry
- Biotechnology - Partners EU based
- Non-Profit Organizations - Contribute to the development of life changing drugs
Pharmaceutical Companies
We support several of the largest pharma companies worldwide from Phase I to Phase IV in various disease areas.
Our services include:
- Analysis and reporting
- Functional sourcing
- Design innovative clinical trials
Why choose us:
- Outstanding ratings
- Competitive rates
- Quality and timeliness
- Small CRO - individual personal relationships and flexibility
We have Master Service Agreements (MSAs) in place to build long term business partnerships.
Smaller Biotech companies partner with us to provide them with a statistical unit/group.
Our support starts at first-in-human to final drug approval.
Our services include:
- Statistical consulting
- Design of studies
- Regulatory approval support
We have several successful partnerships, join us to be the next success story.
We are a statistical partner for one of the largest cosmetic companies.
Our services include:
- Study design
- Analysis and reporting
We provide statistical consulting to private equity and non profit organizations during compound asssessment and clinical development.
Our Partners
To provide quality services to our customers, we remain focused on our core business. We are a true statistical CRO led by statisticians. Over the years, we have built a network of reliable CRO partners that provide high quality services in their specialty areas. These include:
Data Management
Our DM partner offers eClinical Trial services guaranteeing the highest quality of clinical trials data and outputs resulting from a streamlined process from protocol to clinical study report.
Our PM expert ensures Quality, IT, Planning, Record retention and Compliance throughtout the trial period.
Our pharmacokinetic and modeling experts can handle non-compartmental analyses as well as PK/PD modeling projects..
We work with a network or scientific writers who can assist in regulatory documents, and scientific communications.
For regulatory interactions and submissions, our network of regulatory scientists is available in the US and in Europe.
Quality really matters!
Our Green Policy
ClinBAY strives to continually make a difference by contributing to the development of life change drugs, AND is also committed to the protection of the environment and responsible use of natural resources by following a Green Policy. As proactive keepers of the public health and the environment, the ClinBAY team embraces pollution prevention and sustainable development while continually seeking to reduce resource consumption.
We will be pleased to hear about your trial project and provide you with a tailored-made, cost effective biometrics solution.
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