Are you looking to initiate new drug development efforts, accelerate time-to-market, prepare for a pre-approval inspection, audit and enhance your quality systems, onboard new manufacturing sites or partners, or optimize pharmacovigilance? For a single consulting partner to help you ensure safe and reliable access to your much-needed products, choose Validant.
Validant’s partners average over 30 years of experience in the pharmaceutical industry and have held leadership positions at the top pharma companies in the world. They’ve also led hundreds of engagements as consultants to both rapidly growing and large, multi-national pharmaceutical clients.
In addition, the leaders of our partner company, DataRevive, are former regulators from the FDA’s CDER and are expert in optimizing regulatory pathways for pharmaceutical development.
No matter your regulatory, compliance, or quality need, our team has solved challenges like yours before and has the perspective, tools, and hard-won experience to help you progress your products.
Working with Validant, you have access to all the GxP expertise needed to compliantly progress your pharmaceuticals from the preclinical phase to commercialization and distribution. We can be your one partner to turn to for:
Tell us what you’re looking to achieve.We’ll put our experience to work on your specific problem.
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