About Us

Company Profile

Simplify your drug development and regulatory approval process with us!

Plexus supports their clients with wide knowledge in providing consulting services in the field of the nonclinical program for NCE development, including dose-response assessment, pharmacokinetics, regulatory toxicology, mechanistic toxicology, descriptive toxicology, in silico computational toxicology (QSAR) & GLP to the industries like pharmaceuticals, biotechnology (biosimilar & vaccine), herbal, cosmetic and medical device companies. Additionally, to support the conduct of various Non-Clinical studies in rodents and non-rodents, we have collaborations with wide number of CROs / academia which helps the client to ease the process of product development.

PPS experts including European Registered Toxicologists (ERT), offer solutions to complex drug development, toxicological and regulatory issues related to Pre-Clinical development through their technical and regulatory knowledge gained with decades of research experience in various industries & CROs. Because of the experience, knowledge and dedication of PPS, most renowned research partners and business owners trust Plexus Pre-Clinical Services as a preferred research partner for their drug discovery and development services. PPS guides you through every process step, from creating a development strategy to your product being approved and regulated.

We respect your commitment to your product and how vital its success is to both you and the target patient populations. That is why PPS has dedicated itself to offering a level of customer service that is unmatched. We offer complete dedication to your product in every thoughtful exchange and guarantee prompt completion.

Vision :

To be known as a world-class leader in developing strategies that ensure smooth regulatory approvals of quality products.

Mission :

Our mission is to close the knowledge gap between regulatory bodies and industry by providing the best acceptable strategies, experience and understanding of regulatory requirements in pharmaceutical, biotechnology, herbal, and medical device manufacturing sectors, both new and seasoned alike. 

Core Values :

We help businesses by optimising costs and catalyse the development of therapeutic & diagnostic products and medical devices by ensuring a plain sailing regulatory process. 

→ Compliance

Consistent with promoting, preserving, and protecting public health, we guarantee that all of our client's procedures are carried out in compliance with the regulations of the authorities under which we operate.

→ Dynamic

We keep abreast with the changes and developments in the regulatory requirements to be confident about giving the best products to society.

→ Integrity

Respect for others' privacy, consulting experts when needed, and staying out of situations where our interests could be compromised are all ways we uphold our integrity.

→ Innovation

We believe in turning challenges into opportunities, ideas into creative solutions and developing a creative mindset by inspiring innovative action.

→ Transparency

Our culture of working with the customers and each other is based on communication, openness, and collaboration. We encourage and value open and honest communication.