About Us

Pharma Simplified Innovation & Compliance.

Prism Consultancy was established with a comprehensive product portfolio, certified contract manufacturing services, internationally recognized BE/BA study partners, expertise in international regulatory affairs documentation and site variations, and product out-licensing capabilities.

Our core objective is to facilitate the manufacturing of complex products supported by approved and acclaimed BE/BA studies, while also preparing CTD, ANDA, or other country-specific regulatory submissions for seamless approval.

We are committed to delivering exceptional value to our clients by continuously improving our operations, maintaining transparency, and actively engaging with all stakeholders.
By fostering partnerships with companies, providers, managed care organizations, Ministries of Health (MOHs), and non-governmental organizations worldwide, we ensure a collaborative approach to achieving shared success.

Fueling Pharma Partnerships & Solutions

The pharmaceutical industry is undergoing significant shifts due to blockbuster patent expirations, fewer drugs in development, increasing generics, and mounting regulatory pressures—challenging long-standing industry fundamentals.

For generic companies, this presents a vital opportunity to align their marketing strategies and capitalize on both existing and emerging product lines. At Prism Consultancy, we are ready to meet your needs with prompt and tailored solutions.

Our long-term strategy focuses on fostering collaborations with pharmaceutical companies, biotechnology firms, and universities.
We specialize in in-licensing and out-licensing products, developing comprehensive product dossiers, and managing contract manufacturing through India.
By providing end-to-end services, Prism Consultancy ensures value-driven support for all our clients’ requirements.
Scroll to Top