I can thoroughly recommend Nextvel. They are a joy to work with, very professional and helpful. They know their stuff and gently but firmly move you through the process. They have helped us get approval for a clinical trial in India at a very difficult time which required hard work, determination, skill and patience. They are extremely professional to deal with and very pleasant. With Nextvel you are in good hands.

Was a delight to work with Nextvel. The team has a problem-solving approach and always goes above and beyond. It never felt like we were chasing regulatory approval alone, it always felt like a team (MTx and Nextvel) working together towards a goal.

I wanted to take a moment to express my sincere gratitude for the outstanding support you have provided. Your team’s professionalism, expertise, and dedication have truly made a difference in our experience, and we are thrilled with the results achieved through your guidance.

Please extend our thanks to everyone involved in the project. We look forward to future collaborations and will happily recommend your services to others.

Nextvel provided our ophthalmic surgical laser firm with local knowledge of prospective partner candidate medical facilities, they guided us through the Indian regulatory, they organized, supervised, QA’d and libraried all trial data collected for each participating patient – from recruitment through post-op follow-up, and then they analyzed and assembled the trial results in a comprehensive report ready for peer review and publication. They are a professional, comprehensive quality control operation in complete command of the subject matter and ready to deploy on your behalf . We would not have been successful without them.

We are very satisfied with our cooperation

This is to certify that we have used the Regulatory Affairs and Clinical Research Services of Nextvel Consulting LLP since 2012.
Nextvel led by Ms. Mala Srivastava, Co-founder & Managing Partner, has supported us in obtaining the necessary Central Drugs Standard Control Organization (CDSCO) Approvals and Licenses for several stem cell-related products.

We have an excellent record of this collaboration, and we look forward to continuing this relationship in the times ahead.

This is to certify that we used the Regulatory Affairs Services of Nextvel Consulting LLP in the year 2020.
Nextvel led by Ms. Mala Srivastava, Co-founder & Managing Partner, supported us in obtaining the necessary Central Drugs Standard Control Organization (CDSCO) Approvals and Licenses for the product CRISPR-based IVD for SARS-COVID -19 Diagnostic Kit, in record time for timely launch of the product

We had an excellent experience working with Nextvel for obtaining approval for this product.

The extraordinary team of #nextvel consultants led by Mala Srivastava MRQA, led the entire process of the regulatory submission.