We specialize in preclinical safety testing, toxicologic pathology, histopathology evaluations, clinical pathology, and regulatory consulting services.
Yes, we operate in compliance with international regulatory guidelines such as ICH, OECD, FDA, EMA, EU, JMAFF, CIB, and OPPTS.
We follow strict data privacy protocols and confidentiality agreements. All client data is securely stored and never shared without explicit permission.
Simply contact us through our Support page or email us at contact@vedhbioscience.com. We’ll guide you through the onboarding and project initiation process.
Yes, we tailor our studies to meet specific client needs, including custom protocols, endpoints, and reporting formats.
Report delivery times vary by study type, but we maintain a quick turnaround time without compromising quality. Timelines are discussed at the start of each project.
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