Who We Are
Ra Docs Management Services is a Pharmaceutical consulting firm founded in 2017, to provide One stop solutions from SME to large Pharmaceutical manufactures in the field of Technical & Plant Documentation, Certification, Plant designing, GMP compliance, validation. One of the fastest growing Pharma Turnkey Project Consultant based in Ahmedabad, India. We had clear target to attend pharmaceutical manufactures quality & GMP compliance requests and to solve in a quick and economical way.
Over the years we have continuously innovated ourselves, Our qualified team is highly regarded for its creativity, professionalism, and ability to undertake engineering projects from the point of inception to design and through to completion.
Over the years we have continuously innovated ourselves, Our qualified team is highly regarded for its creativity, professionalism, and ability to undertake engineering projects from the point of inception to design and through to completion.
We offers various services from scratch up to start-up, erection & commissioning of new pharmaceutical plant. We are hands-on problemsolvers who realize the fact that each project brings its own set of challenges. After assessing a client’s needs, we assign a project-specific team with expertise needed to provide the best solution and follow it through to a successful conclusion.
Our goal is to provide Economic & State of art pharmaceutical unit with compliance of international standard to our clients. Our team provide technical guidance and project direction working closely with each client to ensure that the client’s needs are fulfilled.
Our goal is to provide Economic & State of art pharmaceutical unit with compliance of international standard to our clients. Our team provide technical guidance and project direction working closely with each client to ensure that the client’s needs are fulfilled.
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."
- Darshit Joshi
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."
- Darshit Joshi
Our Mission
“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.”
Our advice and efforts comes from our work experience, we first listen to you, recognize your needs and then present Quality work, Unmatched client service; Innovative solutions.
Our in house CAD, Engineering Support, Design Installation; Consulting at every step till projects completion will help you to get you the results you want at the budgets and timelines that you may have. We are glad to serve as a Pharmaceutical engineering consulting.
We offers various services from scratch up to start-up, erection & commissioning of new pharmaceutical plant. We are hands-on problemsolvers who realize the fact that each project brings its own set of challenges. After assessing a client’s needs, we assign a project-specific team with expertise needed to provide the best solution and follow it through to a successful conclusion.
So if you are a new manufacturing pharmaceutical unit or want to expand an established business, contact us and find a refreshing approach to your needs.
We offers various services from scratch up to start-up, erection & commissioning of new pharmaceutical plant. We are hands-on problemsolvers who realize the fact that each project brings its own set of challenges. After assessing a client’s needs, we assign a project-specific team with expertise needed to provide the best solution and follow it through to a successful conclusion.
So if you are a new manufacturing pharmaceutical unit or want to expand an established business, contact us and find a refreshing approach to your needs.
Our Expertise
Core regulatory services
Pharmaceutical industries are in a highly regulated environment and require effective document management; technical process.
Documentation is an integral part of good manufacturing practices. It defines a system of information and control so that risks so inherent in misinterpretation and/or error in oral communication are minimized.
It consequently strengthens the quality, and its consistency, of all goods and services, as those responsible for the specific operations have clear, unambiguous instructions to follow including active drug substances, is legally mandatory.
We provide a full range of Food and Pharmaceutical Regulatory Affairs consulting services to the Pharmaceutical, Biotechnology and Healthcare Industries. Our expertise covers all stages of the product lifecycle and each service is delivered by a specialist in their field with the relevant knowledge and experience.
Documentation is an integral part of good manufacturing practices. It defines a system of information and control so that risks so inherent in misinterpretation and/or error in oral communication are minimized.
It consequently strengthens the quality, and its consistency, of all goods and services, as those responsible for the specific operations have clear, unambiguous instructions to follow including active drug substances, is legally mandatory.
We provide a full range of Food and Pharmaceutical Regulatory Affairs consulting services to the Pharmaceutical, Biotechnology and Healthcare Industries. Our expertise covers all stages of the product lifecycle and each service is delivered by a specialist in their field with the relevant knowledge and experience.
