Clinical Study Management
We manage all phase of clinicals trials including Investigator Led Trials. Our Engagements commence with support for sites selection and conclude with the final CSR. We have robust SOPs and systems to ensure protocol adherence, regulatory and GCP Compliance.
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Regulatory Affairs
We provide comprehensive support for Regulatory Affairs including mapping out Regulatory pathways in different geographies and hands-on support for Regulatory Submissions until the final outcome of Applications.
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Technical Writing
We specialize in technical writing services focused on clinical, quality, and regulatory documentation crucial for the healthcare and pharmaceutical industries.
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Quality Assurance
Nextvel specializes in providing a comprehensive suite of Quality Assurance (QA) Audit services aimed at ensuring compliance with regulatory standards and optimizing operational efficiency spanning across diverse products and therapeutics.
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Training
We promote excellence in clinical research through comprehensive training and capacity building programs. Training includes basic and advanced training in Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Good Clinical Laboratory Practice (GCLP), Regulations to enhance knowledge and skills needed for high-quality, compliant clinical research.
read moreI 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.