Streamline Your
Regulatory Process
with Our
Medical Device Experts


Expertise and Experience

At RABT, our Regulatory Consulting services boast extensive experience and knowledge, allowing us to expertly navigate the complex regulatory compliance landscapes. We take pride in developing customized Regulatory Strategies tailored to each client's specific needs, helping them achieve their business goals while adhering to FDA, EMA, and other regulatory guidelines.


Customized Solutions

We understand that every client's product is unique, requiring a personalized approach to regulatory strategy. By conducting in-depth analyses of our clients' products and business objectives, we offer highly customized Regulatory Consulting Services that optimize the entire regulatory process.


Time and Cost Savings

At RABT, we recognize the critical importance of regulatory affairs requirements and strive to simplify the process for faster product approvals. By proactively addressing potential obstacles, we enable our clients to save valuable time and money, allowing them to focus on developing innovative medical products and improving patient outcomes.

Industry-leading Experts


Welcome to the RABT Global

What We Do

RABT Global serves as a trusted partner for life sciences companies, providing a comprehensive range of Regulatory Consulting services designed to ensure regulatory compliance with global regulations, expedite approvals, and maximize market opportunities.


Our unique and efficient Regulatory Consulting services structure enables us to deliver quick and tailored solutions to clients of all sizes. We fully understand that each client has distinct goals, which is why we offer solutions based on their readiness and immediate as well as long-term objectives.

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Call to Our Experts



Reasons to Choose RABT Global as Your Lifesciences Regulatory Partner

  • Regulatory Expertise

    Regulatory Expertise

  • Tailored Solutions

    Tailored Solutions

  • Comprehensive Services

    Comprehensive Services

  • High-Quality Services

    High-Quality Services


With our unmatched expertise and meticulous approach, we empower life sciences organizations to confidently navigate regulations, gain efficient approvals, and seize market opportunities

End-to-end Registration services

As the Life Sciences market is projected to reach $4.2B by 2024, the need for compliant products with global accessibility and regional regulatory compliance is critical for pharma, biotech, medical devices, and healthcare organizations. RABT offers end-to-end regulatory services to address these demands.

Medical Communications

At RABT, we combine therapeutic expertise with innovative approaches to establish meaningful connections with data, engaging patients, caregivers, and physicians through exceptional medical communication services and a comprehensive regulatory strategy.

Other Regulatory Services

Our regulatory consulting services extend to the global life sciences industry. We focus on reducing costs and time to market through flexible, information-based services. Our regulatory consultants offer expertise for product lifecycle management and submission strategies.

Legal Representation

Supporting global pharmaceutical companies, CROs, CDMOs, and other service providers, RABT's regulatory team, with extensive industry experience, offers nimble and cost-effective services, setting us apart from traditional law firms.

US Agent Services

US Agent

For foreign manufacturers of devices to be imported into the US, having a US agent to communicate with the FDA is crucial. Our team assists with registration, documentation, and ongoing compliance support.


Our regulatory affairs team ensures the safety and efficacy of pharmaceutical products by managing post-approval CMC and the life cycle. We adeptly handle regulatory submissions and stay updated with all requirements. Contact us for comprehensive support.

Product-Specific Guidance on Generic Drug Development


The pharmaceutical industry must adhere to EMA guidelines on HBEL to prevent toxicological risks. Establishing a substance-specific safe dose known as PDE requires rigorous pharmacological and toxicological data evaluation. RABT's expert toxicologists can assist with cleaning validation and regulatory compliance.

Translation Services

Language Scientific provides accurate medical translation services, backed by a Quality Control system ensuring education, training, and experience matching the subject matter. Our services are trusted by pharmaceutical companies, CROs, biotech companies, and healthcare managers.

Contact us today to discuss how our tailored regulatory solutions can streamline your compliance process.

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