ISO 17025 CRO (MENA & EU): Cloud based lab, Pharma Validation, CRMs & Pre-clinical Studies

WHO WE ARE: Nawah Scientific is a premier Contract Research Organization (CRO) and ISO 17025 accredited SME operating across the MENA & EU. As a Horizon Europe Associated Country partner, we bring full funding eligibility and a unique "Cloud Lab" infrastructure that processes over 1 million samples annually.

OUR VALUE PROPOSITION: We offer Health Consortiums a "One-Stop-Shop" for Analytical Validation, bridging the gap between drug discovery and clinical trials.

TECHNICAL EXPERTISE (OFFERED SERVICES):

1. In Vivo Pre-clinical Validation (Animal Models):

• Pharmacokinetics (PK/PD): Bioanalysis via LC-MS/MS for plasma/tissue distribution (Oral, IV, IP) in rodent models.

• Disease Models: Validated models for Oncology, Metabolic Syndrome, and Inflammation.

• Safety Studies: Acute/Chronic toxicity testing and Histopathology.

2. In Vitro (Cell-Based) & Molecular Bioassays:

• Cell-Based: High-throughput screening for Cytotoxicity (MTT/SRB), Cellular Uptake, Permeability (Caco-2), and Flow Cytometry.

• Molecular: Quantitative Gene Expression (qPCR), Protein Analysis (Western Blot), and ELISA markers.

• Microbiology: Antiviral (BSL-2/3) and Antibacterial profiling (MIC, Biofilm).

3. Pharma CRMs & Hit-to-Lead Chemistry:

• Certified Reference Materials: Custom synthesis and certification of pharmaceutical impurities and standards.

• Characterization: Full structural elucidation using NMR, XRD, and Mass Spectrometry.

4. Advanced Nano-Formulation:

• Nanotechnology: Design and characterization of Liposomes, PLGA nanoparticles, and Solid Lipid Nanoparticles (SLNs).

WHY PARTNER WITH NAWAH?

• Dual Reach (MENA & EU): Direct access to diverse biological samples and regional markets via our Egypt and Poland offices.

• Regulatory Ready: ISO 17025 accreditation ensures data acceptance for regulatory filings.

• Speed: Centralized Cloud Lab model accelerates TRL advancement.

LOOKING FOR: We are seeking to lead Work Packages in:

• Pre-clinical Validation (In Vitro/In Vivo)

• Standardization & Quality Control

• Bioassay Development & Screening