Our Location
Debo Industrial Compound, Oshodi Apapa Expressway, Oshodi, 102215, Lagos, Nigeria
Comprehensive Clinical Research. Regional Expertise.
Accelerating drug development through expert-led clinical trials, cutting-edge laboratory infrastructure, and regulatory compliance — right here in Nigeria.
Comprehensive Clinical Research. Regional Expertise.
Accelerating drug development through expert-led clinical trials, cutting-edge laboratory infrastructure, and regulatory compliance — right here in Nigeria.
Who We Are
Regulatory Affairs
- Ethics committee submissions
- Bioequivalence (BA/BE) study approvals
- Local regulatory support for new therapies
- Note: Ethics approvals are already in place. NAFDAC registration is in progress.
Bioanalytical & Laboratory Services
- Sample reception and management
- LC-MS/MS-based drug concentration and stability testing
- Method development and validation for generics and novel molecules
- Note: We accept all valid samples and provide complete analytical support.
Data Services
- Electronic Data Capture (EDC) systems
- Biostatistics and data interpretation
- Clinical Study Report (CSR) generation
- Medical and regulatory writing
Post-Marketing & Pharmacovigilance
- Real-world data collection
- AE/SAE monitoring
- Compliance reporting and signal detection
Facilities
Location
Debo Industrial Compound, Oshodi Apapa Expressway, Oshodi, 102215, Lagos, Nigeria
Technology Highlights
- Dedicated laboratories for microbiology, analytical chemistry, and pharmacokinetics
- Advanced LC-MS/MS, HPLC, ELISA, and cold-chain equipment
- Electronic Data Capture systems and secure, audit-ready storage
- Full medical facility to manage trial-related contingencies onsite
Scalability & Throughput
Our lab supports same-day sample processing and concurrent project execution. High-throughput instrumentation allows us to handle large trial volumes while maintaining precision and regulatory compliance.
Commitment to Ethics & Patient Safety
Patient safety is the cornerstone of every study at BioQuest. All clinical research is conducted under strict ethical protocols, with transparency, informed consent, and data confidentiality at the core.
We provide a full spectrum of services — from study planning and bioanalysis to regulatory guidance — backed by our advanced facilities in Lagos and a team of skilled scientists, analysts, and compliance professionals.
Mission
To support local and global pharmaceutical innovation through precise, ethical, and efficient research solutions.
Vision
To be West Africa’s most trusted and technologically advanced CRO, bridging global standards with regional insight.
Core Values
- Precision
- Integrity
- Speed
- Innovation
- Collaboration
Leadership
Dr. Obiefuna Ajie brings a clinical perspective with MBBS in Medicine & Surgery from the University of Nigeria and an M.Sc. in Pharmacology (University of Lagos). As an accomplished Researcher at the University of Lagos, he offers valuable insights in medicine and pharmacology, strengthening Bioquest's medical research initiatives.
Dr Mr. Benedict Agbo is a seasoned professional with extensive academic and cross-disciplinary expertise. He holds a B.Sc. in Biochemistry, a Master’s degree in Pharmaceutical Chemistry, and an additional Master’s in International Law and Diplomacy. He also earned a PhD in Biochemistry with a specialization in Molecular Biology. Mr. Agbo provides strategic oversight grounded in both scientific rigor and regulatory insight.
Mr. Uday Balasaheb Sawant brings a comprehensive background in clinical operations and quality assurance, holding a B.Sc. in Zoology and a Post Graduate Diploma in Clinical Studies, Data Management, and Medical Writing. Formerly a Manager of Quality Assurance at AnaZeal Analyticals & Research and a Senior Officer at TEVA Pharmaceuticals, he offers extensive experience in managing complex BA/BE studies and ensuring regulatory compliance with bodies like the USFDA, UKMHRA, Chile OEDC and WHO. His deep expertise in clinical trial coordination and audit management strengthens organizational efforts in maintaining high-quality research standards and operational excellence.
Mr. Balaji Nagaraj brings extensive technical expertise as a Bioanalytical Scientist with over 10 years of experience in method development, validation, and sample analysis. Holding a Master of Pharmacy from J.K.K. Muniraja College of Pharmacy, he has built a robust career across several research institutions, including roles as a Research associate at Axis Clinicals and Aizant Drug Research. He is very proficient in LC-MS/MS and regulatory compliance (FDA, EMA, & ICH).
Our Services
Clinical Trial Management
- Study planning and protocol development
- Site selection, investigator engagement
- Monitoring, documentation, and study closeout
Regulatory Affairs
- Ethics committee submissions
- Bioequivalence (BA/BE) study approvals
- Local regulatory support for new therapies
- Note: Ethics approvals are already in place. NAFDAC registration is in progress.
Bioanalytical & Laboratory Services
- Sample reception and management
- LC-MS/MS-based drug concentration and stability testing
- Method development and validation for generics and novel molecules
- Note: We accept all valid samples and provide complete analytical support.
Data Services
- Electronic Data Capture (EDC) systems
- Biostatistics and data interpretation
- Clinical Study Report (CSR) generation
- Medical and regulatory writing
Post-Marketing & Pharmacovigilance
- Real-world data collection
- AE/SAE monitoring
- Compliance reporting and signal detection
Facilities
Location
Debo Industrial Compound, Oshodi - Oworonshoki Expressway, Papa Ajao, Lagos 102215, Lagos, Nigeria
Technology Highlights
- Dedicated laboratories for microbiology, analytical chemistry, and pharmacokinetics
- Advanced LC-MS/MS, HPLC, ELISA, and cold-chain equipment
- Electronic Data Capture systems and secure, audit-ready storage
- Full medical facility to manage trial-related contingencies onsite
Scalability & Throughput
Our lab supports same-day sample processing and concurrent project execution. High-throughput instrumentation allows us to handle large trial volumes while maintaining precision and regulatory compliance.
Commitment to Ethics & Patient Safety
Patient safety is the cornerstone of every study at BioQuest. All clinical research is conducted under strict ethical protocols, with transparency, informed consent, and data confidentiality at the core.
Our commitment ensures confidence for trial participants, investigators, sponsors, and regulators alike.
Contact
Contact Us
We’re ready to support your clinical research. Reach out to explore how BioQuest can become your research partner.