(CRO) Contract Research Organization in Delhi NCR, India - Frontro Pharma

Welcome to FrontroPharma, a contract research organization in Delhi, India is your gateway to innovative solutions in clinical & contract research organization (CRO) services. Explore our diverse expertise across the pharmaceutical spectrum:

Product Development

Harness scientific prowess with our CRO team excelling in Nano formulations and liposomes. We optimize drug delivery systems, ensuring precision in complex generics, AYUSH products, nutraceuticals, and cosmetics. Our rigorous scientific approach transforms your concepts into cutting-edge formulations, ensuring efficacy and excellence in every product we develop.

Preclinical Study

Trust us for thorough preclinical safety and efficacy evaluation studies. Our in vivo model assessments cover a spectrum of conditions, including

Detailed histopathological and immunohistochemical assessments are integral components of our evaluations.

Analytical Technique

Rely on our one-stop solution for all analytical techniques related to product development and evaluation. We offer comprehensive services, including.

Regulatory and Scientific Writing

Navigate the complex world of regulatory requirements with ease. Our experts specialize in preparing and reviewing regulatory documentation. Whether it’s narratives, systemic reviews, meta-analyses, grant writing, or project consultations, we have the skills to articulate your scientific endeavors effectively.

At FrontroPharma, we blend scientific prowess with a commitment to excellence, ensuring your journey from concept to market is seamless and successful—partner with us for a transformative CRO experience.

Regulatory Filing

We’re your expert guide for regulatory filing, helping you navigate these twists and turns with clarity and confidence.

We understand the global regulatory landscape – each country’s different rules and requirements. We also know the ins and outs of different drug types, from rare diseases to everyday medications. This deep knowledge lets us create a clear path for your drug, ensuring all the paperwork is in order and every step meets the standards.

Think of us as your friendly neighbors who are regulatory geniuses. We’ll handle the heavy lifting

Planning your approval journey: We'll map out the best route, considering all the twists and turns of regulations.
Managing your clinical trials: We'll ensure your studies are done right, following all the rules and collecting the correct data.
Putting together your application: We'll gather all the necessary information and package it up perfectly for the authorities.
Submitting your application and dealing with any questions: We'll be your voice, ensuring your drug gets the attention it deserves.
Helping you after approval: We'll stick with you to handle any changes or updates that might come up.

With Frontro Pharma, you don’t have to wander the regulatory maze alone. We’ll be right there with you every step of the way until your drug reaches its destination – the market.

Ready to ditch the confusion and embrace clarity? Contact Frontro Pharma today. We’ll help you turn that regulatory maze into a smooth highway to success.