RanX was founded on the belief that partnerships are long-term alliances based upon client needs, quality, cost, and above all, trust.

 

We are a renowned team of highly experienced and dedicated scientists coupled with state-of-the-art cGMP facility with R & D capabilities. We thrive to become one of the preeminent providers of product development services for pharmaceutical industry, specializing in drug delivery technologies for pharmaceutical products locally and globally.

​

Our focus on the development process spans from strategy, through implementation, delivering a stable, bio-available, scale-able and commercially viable dosage forms for use in clinical trials and registration.  RanX’s quality consciousness certainly complements our relationship with every quality-conscious customer and manufacturer.

​

Our product development capabilities encompass a full range of solid dosage forms for oral delivery using proprietary technologies. We offer cGMP manufacturing capabilities for clinical supplies of NCEs and blinding of comparators.  Our analytical capabilities range from transfer and qualification of an existing method to complete method development and validation for drug substance, drug product and cleaning verification. Also, RanX offers ICH stability condition storage and analytical testing for drugs.

​

We live up to our customer's trust to provide reliable and timely development. We are well positioned to partner with multinational and small companies alike.  And rest assured that RanX's practices meet cGMP and FDA mandates for pharmaceutical product development to assure quality, safety and efficacy of pharmaceuticals products.