Regulatory Beyond Borders Expectations Excellence Standards

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

Company News

RegBridge Becomes ISO 9001:2015 Certified

We are proud to announce that RegBridge has achieved ISO 9001:2015 certification in the field of Regulatory Affairs services through an audit conducted by UKAS-accredited certification body, Intertek.

ISO 9001 standard is an internationally recognized standard, ensuring that our Quality Management System (QMS) meets the highest global benchmarks for quality management and customer satisfaction. It reflects our commitment to delivering excellence and adhering to best practices worldwide by continuous improvement in business operations.

This milestone is a result of our robust internal processes, commitment to innovation, and unwavering focus on quality. It empowers us to refine our operations and maintain the highest standards across processes and teamwork.

We believe that achieving ISO 9001:2015 certification strengthens RegBridge's market position as a dynamic and fast-growing service provider. This accomplishment underscores our unwavering commitment to our core values: Guaranteeing Compliance, Ensuring Quality, Respecting Timelines, Delivering Client Satisfaction, Fostering Integrity, and Empowering Accountability, which guide every aspect of our operations and services.

Establishing Our European Presence: RegBridge in Estonia

RegBridge is pleased to announce the establishment of its new office in Tallinn, Estonia – marking a significant step in the company's strategic growth and commitment to strengthening its presence across Europe.

This expansion reinforces RegBridge's mission to drive regulatory excellence and streamline market access for life-saving medicines within the EU. Estonia's advanced digital infrastructure, transparent regulatory environment, and growing pharmaceutical ecosystem make it an ideal hub for delivering high-quality regulatory affairs, pharmacovigilance, and compliance solutions.

“Establishing a presence in Tallinn is a strategic milestone and reflects our dedication to serving clients across Europe with even greater accessibility and efficiency.” said Nargiz Asgarova, Founder and CEO of RegBridge. “We are eager to cultivate new partnerships within the Baltic region and remain committed to delivering the high-touch, expert-driven solutions to our clients worldwide to help them navigate complex regulatory landscapes.”

Global Reach Expands: RegBridge Launches Regulatory and Pharmacovigilance Services in Türkiye

RegBridge is pleased to announce the strategic expansion of its regulatory and pharmacovigilance service offerings to Türkiye. This launch marks a significant milestone in the company's global commitment to supporting pharmaceutical and biotech clients in high-growth, strategically vital markets.

Türkiye is recognized as a regional powerhouse with a dynamic regulatory landscape and a rapidly developing pharmaceutical sector. By extending its services to this market, RegBridge aims to provide crucial local expertise, enabling clients to navigate the country's compliance requirements and bring essential products to market efficiently and in full regulatory alignment.

“Our vision is to become the preferred global partner by setting gold standards in regulatory affairs, pharmacovigilance, and customer service,” said Nargiz Asgarova, CEO of RegBridge. “With a dedicated team of experts, we aim to bring that excellence to every region we serve – now including Türkiye.”

RegBridge Expands Global Footprint: Now Serving the UK and EU

RegBridge is pleased to announce the strategic expansion of its regulatory and pharmacovigilance services into the United Kingdom and the European Union.

Originally established as a regional consultancy specialized in the CIS and EAEU, with further development in Türkiye, RegBridge has evolved into a global partner operating across borders. This milestone reinforces our mission to connect pharmaceutical companies with both emerging and established markets, ensuring safe, compliant, and timely patient access worldwide.

As an ISO-certified organization, this growth reflects our commitment to quality, compliance, and integrity. We extend our gratitude to our dedicated team and partners for their role in our continuous advancement and for upholding the highest standards of excellence in every territory we serve.

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.

We are committed to staying at the forefront of the regulatory and pharmacovigilance field, continuously implementing the latest industry advancements to deliver the highest standard of service. RegBridge specializes in offering comprehensive regulatory and pharmacovigilance services to pharmaceutical companies operating in the CIS, EAEU, Turkey, UK and EU regions. Our goal is to be the trusted partner in your journey towards regulatory success. With over a decade of experience, 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 and pharmacovigilance 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.

Operating under a one-window governance model, RegBridge ensures streamlined project management while retaining the flexibility to customize services, meeting each client's unique needs. We are a client-focused company, guided by our core values of quality, compliance, and timely delivery with a 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.

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 medicine, while prioritizing patient safety and supporting their safe and effective use throughout the product lifecycle.

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

Türkiye

European Union

United Kingdom

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.

Zehmet olmasa bu bolmeni doldurun