Nawah Scientific

Nawah Scientific is a premier Contract Research Organization (CRO) and ISO 17025 accredited SME operating across the MENA region and the 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 for clients in 30+ countries.

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

TECHNICAL EXPERTISE (OFFERED SERVICES):

1. Pharma CRMs & Chemistry (Hit-to-Lead):

• Certified Reference Materials: Custom synthesis and certification of pharmaceutical impurities and standards to ensure regulatory compliance.

• Structural Characterization: Full elucidation using high-end NMR, XRD, and Mass Spectrometry.

2. In Vitro & In Vivo Pre-clinical Validation:

• High-Throughput Screening: Cytotoxicity (MTT/SRB), Antiviral (BSL-2/3), and Antibacterial profiling (MIC/Biofilm).

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

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

3. Advanced Nano-Formulation:

• Nanotechnology: Design and characterization of Liposomes, PLGA/PLA nanoparticles, and Solid Lipid Nanoparticles (SLNs) for targeted drug delivery.

WHY PARTNER WITH NAWAH?

• Dual Reach (EU & MENA): With offices in Poland and Egypt, we provide a gateway to diverse biological samples and regional markets while maintaining strict European quality standards.

• Regulatory Ready: All workflows are governed by ISO 17025 and GLP-aligned protocols.

• Speed: Our centralized Cloud Lab model accelerates TRL advancement by reducing validation timelines by up to 40%.

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

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

• Standardization & Quality Control

• Nano-medicine & Formulation Development