One-Stop Pharma Compliance Experts
Ra Docs Management Services, founded in 2017, is a leading Pharmaceutical consulting firm based in Ahmedabad, India. Specializing in Technical & Plant Documentation, Certification, Plant Designing, GMP Compliance, and Validation, we provide end-to-end solutions for pharmaceutical manufacturers. Our expert team is dedicated to delivering innovative, economical, and compliant turnkey project solutions, ensuring that each client’s unique needs are met with professionalism and precision.
Shaping Radocs’
Foundational Pillars
Our Mission
To empower pharmaceutical manufacturers by delivering innovative, end-to-end solutions that bring ideas to market. We’re dedicated to ensuring your success through quality, efficiency, and unwavering support.
Our Vision
To be the trusted leader in pharmaceutical engineering, setting the benchmark for excellence and innovation, while driving the right guidelines in every project we undertake.
Our Expertise
Harnessing deep industry knowledge, we specialize in regulatory services, CAD design, and comprehensive project management. From inception to completion, our tailored approach ensures that your projects are completed on time and within budget.
Our Values
We are committed to integrity, collaboration, and a passion for excellence. All projects reflect our dedication to client’s satisfaction and the belief that every challenge is an opportunity to grow.
Complete Pharmaceutical Consulting Solutions
“We are here to work with our clients to construct, develop their manufacturing facility to global standard by providing end to end solutions of their project needs as for our Pharmaceutical engineering consultants worldwide.”
Clinical Research
Documentation
It is essential evidence for quality assurance as well as for meeting all MHRA requirements.
Drug Master File
Explains the chemistry, manufacturing, & control of an active pharmaceutical ingredient.
CTD Dossiers
It is a set of comprehensive specifications for the registration of pharmaceutical medicines.
Turnkey Pharma Project
Civil design, electrical engineering, third party inspection, and more for your pharmaceutical projects.
Director's Message
“We can assist with project management and registration of such products and have valuable experience in this area.
We can work with you to guide you through the necessary requirements under the Directive that you will have to comply with. We can either prepare for you or help you to preparea submission for a traditional herbal medicinal product, including vital presubmission discussions with the Health Authorities.”
Presenting our
Prestigious Clientele
Our team practices active listening to deliver quality work that precisely meets your needs. We collaborate with clients to construct and develop manufacturing facilities to global standards, and our solutions adhere to all requirements from scratch to launch in the pharmaceutical regulation industry.
