Regulatory Beyond Borders Expectations Excellence Standards

RegBridge is one-window outsourcing regulatory service provider for BioPharma and MedTech companies,
focusing on customer needs and access of patients to essential medicines.

WHO WE ARE

We are committed to staying at the forefront of our field, implementing the latest industry advancements to provide you with the best service possible.

RegBridge specializes in offering comprehensive regulatory and pharmacovigilance services to pharmaceutical companies operating in the CIS region, including also Mongolia, Moldova and Russia. Our goal is to be the trusted partner in your journey towards regulatory success. With over a decade of experience and expertise, our highly qualified team is dedicated to assisting you in achieving your business objectives.

With a comprehensive suite of services tailored to the unique regulatory landscape of each country, we empower companies to navigate complex processes with confidence and efficiency, enabling them to successfully launch their products in the region. When necessary, we collaborate closely with marketing and supply chain departments .

We operate on a one-window governance model, ensuring efficient project management while retaining the flexibility to customize services, meeting our clients' unique needs. Our company is client-oriented, placing a strong emphasis on quality, compliance, and delivering on time with high sense of accountability and integrity.

Values

We ensure the highest standards in every aspect of our services.

Guaranteeing Compliance

Regulatory compliance is not just a goal, it's our promise. With a comprehensive understanding of the ever-evolving landscape of pharmaceutical regulations, we provide expert guidance and solutions to navigate complex compliance requirements seamlessly. Trust us to keep your operations in full adherence, mitigating risks and ensuring a smooth regulatory journey.

Ensuring Quality

Our commitment to quality is the bedrock of our operations. Every task, from consultation to delivery, is infused with an unwavering dedication to maintaining the highest standards. This commitment ensures that your pharmaceutical endeavors meet and exceed regulatory requirements, providing a foundation of trust for all stakeholders involved.

Respecting Timelines

In the fast-paced world of pharmaceuticals, time is of the essence. Our agile approach and finely-tuned processes are designed to deliver results promptly. From consultation to project completion, we understand the urgency and ensure that tasks are completed efficiently, allowing you to stay ahead in a competitive market.

Client Satisfaction

Ensuring client Satisfaction is one of the main values of our company. We prioritize meeting and exceeding our clients' expectations, gaining their trust and loyalty.

Fostering Integrity

Integrity is a cornerstone value of our company. We believe in conducting business with honesty, transparency and a strong sense of ethics. It guides every decision we make, ensuring that we always act in the best interests of our clients and partners.

Empowering Accountability

By upholding the principles of accountability, we ensure that every interaction, project, and endeavor results in improved outcomes and strengthened partnerships. We understand that accountability isn't just a word—it's a promise we live by, delivering exceptional results and building lasting trust with those we serve.

Mission and Vision

Facilitating regulatory compliance and market access for pharmaceutical companies across the world.

OUR MISSION

Is to provide expert guidance and tailored solutions in regulatory and pharmacovigilance services that streamline the approval process and facilitate market access, ensuring rapid, consistent and sustained access of patients to essential medicines.

OUR VISION

Is to be the preferred partner globally, through excellence in regulatory, pharmacovigilance and customer service. With a dedicated team of experts we aspire to set gold standards for the industry.

Our Services

REGULATORY AFFAIRS

Regulatory services across the region covering the full scope of services from dossier development to full lifecycle management. Read more

PHARMACOVIGILANCE

Comprehensive local and regional pharmacovigilance services, including QPPV and LPPV support, with dedicated safety management throughout the pre- and post-authorization stages of the product lifecycle. Read more

Service Area

Azerbaijan

Belarus

Georgia

Kazakhstan

Kyrgyzstan

Moldova

Mongolia

Russia

Tajikistan

Turkmenistan

Ukraine

Uzbekistan

Blogs

Are You Ready for EAEU? Countdown to the Deadline – December 31, 2025 Current Status and Next Steps Checklist. As the deadline of December 31, 2025 approaches for bringing all medicinal products into compliance with Eurasian Economic Union (EAEU) requirements, otherwise called as upgrade procedure, it’s crucial to assess the current status and outline the next steps.

Join Our Team

Join our dynamic team and be a part of
revolutionizing pharmaceutical regulatory services across the world.

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