Want to gain expert guidance right from the beginning with early discovery to post-approval life-cycle management? Look no further...

We mitigate risks in the initial stages and ensure that your product is safe to use globally after the safety evaluation...

PPS offers complete medical device & its packaging material evaluation in compliance with ISO and ASTM, which includes biocompatibility and chemical characterization [Extractables & Leachables (E&L) analysis] in collaboration with our partner’s state-of-the-art laboratories

PPS brings you a team consisting of European Registered Toxicologist (ERT) / Diplomate of American Board of Toxicology (DABT) to assess various necessary aspects required to ensure a thorough toxicology risk assessment

Need help to implement a systematic quality assurance diligently and vigilantly that ensures no roadblocks in the product development process? Plexus has got you covered.

Be it expert reviews on available toxicopathology data or assistance in regulatory query replies, we provide end-to-end Histopathology support.

We personalise the regulatory service and support process for product approvals ensuring that your product obtains approval for regulation on the first attempt.

We set up or upgrade a laboratory animal breeding facility, ensuring that all the major and minor requirements are taken care of.

We know what it takes to build an optimal GLP test facility and to have certification. We assist you in the entire process right from planning and setting up GLP systems at test facilities including QMS to training the staff. We also assist in drafting application for GLP certification and submission of ATR for observations.