Ovi Consultancy Services is a trusted Pharmaceutical and Healthcare consultancy specializing in Bioavailability/Bioequivalence (BA/BE) studies, Clinical Trials, Pre-clinical research, Regulatory Compliance, and Data Integrity solutions. With a team of experienced scientists, regulatory experts, and project managers, we provide end-to-end support to pharmaceutical, biotech, medical device, herbal, and nutraceutical companies.

We are committed to Innovation, Compliance, and Quality while helping businesses navigate complex regulatory landscapes and achieve successful product development and approval. Our expertise spans scientific research, regulatory strategy, technology-driven solutions, and operational excellence, ensuring that our clients stay ahead in the competitive healthcare industry.

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Get to know us

Ovi Consultancy Services aims to be a globally trusted partner in pharmaceutical research, regulatory compliance, and healthcare innovation, providing high-quality, technology-driven solutions that ensure efficiency, compliance, and scientific excellence.

Our Vision

Our mission is to deliver comprehensive consultancy services in BA/BE studies, clinical trials, regulatory affairs, and data integrity, empowering pharmaceutical and healthcare companies with cost-effective, compliant, and scientifically sound solutions for successful product development and approvals.

Our Mission

At Ovi Consultancy Services, we take pride in our Highly Skilled and Experienced Team of Professionals dedicated to delivering Scientifically Sound, Regulatory-Compliant, and Technology-Driven Solutions for the Pharmaceutical and Healthcare Industries. Our team comprises Clinical Research Experts, Quality Assurance Specialists, Regulatory Professionals, Scientists, Medical Writers, Biostatisticians, and IT Specialists, each bringing Deep Expertise in their respective fields. With a strong foundation in Bioavailability/Bioequivalence (BA/BE) Studies, Clinical Trials, Regulatory Compliance, and Data Integrity, our Experts ensure Seamless Project Execution while maintaining Global Quality and Ethical Standards. Their collective experience spans Drug Development, Study Design, Pharmacokinetics, Regulatory Submissions, Data Management, and System Validation, making Ovi Consultancy Services a Trusted Partner for Pharmaceutical and Healthcare Organizations.

Our Team

Leading our team is Mr. Ninad Potdar, Founder of Ovi Consultancy Services, who brings Over 20 Years of Experience in Clinical Research and has been a Consultant in the Field for More Than Five Years. His expertise covers BA/BE Studies, Clinical Trial Management, Regulatory Affairs, Pharmacokinetics, and Project Execution, making him a Trusted Advisor for Pharmaceutical and Biotech Companies. Under his leadership, Ovi Consultancy Services has successfully guided multiple organizations in Setting Up CRO Facilities, Securing Regulatory Approvals, and Ensuring High-Quality Research Outcomes. With a strong focus on Innovation, Compliance, and Scientific Excellence, Ninad continues to drive the company’s vision of being a Global Leader in Pharmaceutical Research Consultancy.

Mecure Industries PLC, Lagos, Nigeria

Ovi Consultancy Services successfully guided Mecure Industries PLC in establishing a state-of-the-art Contract Research Organization (CRO) and launching Bioequivalence (BE) studies in Lagos, Nigeria. Our expertise covered facility setup, regulatory compliance, quality system implementation, staff training, and study execution support, ensuring global research standards.

With our support, Mecure Industries PLC secured all necessary approvals and has now started conducting BA/BE studies at its newly established facility. This achievement marks a major milestone in advancing Clinical Research capabilities in Nigeria and positioning Mecure as a poineer and a key player in the industry.

Success Story