Careful selection
Role-appropriate qualifications and experience, verified before assignment.
About Bpharma
One accountable partner across the trial and product lifecycle
Bpharma supports sponsors, pharmaceutical and biotech companies, global CROs and research institutions through four specialised divisions. Each division works with its own specialists and points of contact, under one set of quality and ethical standards.
SMO · About us
A strategic partner at the research site
Clinical trials succeed when research sites are well supported — with capable people, dependable coordination and an unwavering commitment to participant safety and data quality.
Who we are
Bpharma SMO supports Principal Investigators, sponsors and CRO partners with flexible, professionally managed site-level solutions. As part of Bpharma, alongside our CRO, Regulatory Affairs and pharmacovigilance teams, we combine clinical research experience, qualified personnel and structured oversight to help sites work efficiently — and responsibly.
SMO · Our people
Qualified people, continuously developed
GCP training, kept current
Documented Good Clinical Practice training for every team member.
Protocol-specific preparation
Study training completed before any study task begins.
Supervision & development
Ongoing guidance, feedback and opportunities to grow.
SMO · Who we support
Value for every partner in the study
Investigators & sites
- Extra capacity without compromising quality
- Trained staff ready for protocol tasks
- More time for medical judgement and participant care
Sponsors
- Dependable site operations and data quality
- Documentation that supports inspection readiness
- Local insight across our region
CROs
- Flexible resource for start-up and peak workload
- Aligned communication with monitoring teams
- Consistent standards across sites
CRO · About Bpharma
Born in the region. Built for collaboration.
An independent research partner that brings regional familiarity to international standards.
A regional Clinical Research Organisation (CRO) with a scientific mindset and a collaborative way of working.
Bpharma CRO brings together clinical operations, medical and scientific expertise, legal and data protection support, and local research-site insight — helping sponsors and CRO partners navigate the realities of clinical research in our region.
Bpharma CRO understands the region from within: its healthcare systems, investigator communities, regulatory context and everyday operational realities.
We support sponsors, biotech companies, academic institutions and global CROs with responsive, professionally coordinated clinical research services. Our approach is grounded in ethical responsibility, quality and the belief that open dialogue leads to better study decisions.
Research integrityRegional perspectiveCollaborative delivery
Medical understanding + practical execution
CRO + SMO / Complementary strengths
Closer to sites. Closer to study reality.
The Bpharma SMO structure provides valuable local understanding that informs CRO planning.
Realistic feasibility
Site familiarity can help reveal operational limits, investigator availability and realistic recruitment considerations.
Practical study coordination
Study planning benefits from seeing the realities of the research site.
Site experience supporting CRO decisions
CRO and SMO service responsibilities remain distinct.
Regulatory Affairs · About us
Regulatory expertise connected to the full research journey
A dedicated regulatory practice within Bpharma’s four-division structure.
Regulatory Affairs at Bpharma supports life-science companies in understanding and navigating the documentation, licensing and post-approval obligations of medicinal products.
Our approach combines scientific insight, experienced regulatory professionals and access to in-house legal expertise — including specialist knowledge of the General Data Protection Regulation (GDPR) and Türkiye’s data protection law (KVKK).
Scientific thinking
Evidence-led assessment.
Legal perspective
Data protection and compliance insight.
Project-specific support · Transparent communication · Thoughtful regulatory strategy