Ensuring compliance and effective communication in pharma services.

We deliver local and regional regulatory affairs and pharmacovigilance support, accompanied by medical and technical writings, professional translations and eCTD dossier preparation services.

Our services

Committed to your product wellness journey: a legacy of care and expertise.

Regulatory affairs

You are starting your first new product or manage multiple product portfolio using RIMS and AMS? EVIGROW offers extensive knowledge of local regulatory requirements and experience with electronic management systems. Our regulatory experts will support you during all the product journey on one local market or on all markets we cover. Starting from regulatory intelligence, technical writings, and ending with timely submissions and approvals.

Pharmacovigilance

EVIGROW established a compliant pharmacovigilance system based on policies and standard procedures, easy integrates with Clients’ pharmacovigilance systems. EU QPPV office will assure overview and take care about your PV system and assure of timely reaction and management of safety issues. ISO 27001 certification on Information security and GDPR implementation assures, proper management of safety information, including personal data.

Medical & technical writings

Partner with EVIGROW for complete CTD dossier writing services. Our integrated approach bridges medical insights and technical expertise, delivering consistent, robust modules across all dossier. Simplify the regulatory process, reduce time to submission, and ensure every document reflects your commitment to quality and compliance.

Why EVIGROW?

We’ve built strong industry connections and a reputation for success, ensuring smooth and timely submissions & approvals.

Our intelligent solutions seamlessly integrate with Clients' systems, streamlining processes and enhancing efficiency. 

Streamlined regulatory solutions.

From documentation to project coordination, ensuring your products meet all standards efficiently.

Safe & compliant pharmacovigilance.

Stay ahead of safety requirements with our comprehensive pharmacovigilance support.

Precision in translation services.

Accurate, industry-specific translations for regulatory, pharmacovigilance, and clinical trials. Our professional team ensures that your documentation is clear, compliant, and reliable.

Your partner in medical & technical writings.

We offer expert knowledge enhanced by innovative solutions that increases efficiency while maintaining the exceptional service your business deserves.

Our achievements

Our journey of success.‍

Our journey in pharmacovigilance and regulatory affairs has been driven by an unwavering commitment to safety and compliance. From our humble beginnings, we recognized the critical need for robust regulatory solutions in the ever-evolving landscape of healthcare.

Successfully partnerships, including major pharmaceutical corporations.

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Products SKUs covered by EVIGROW services.

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Number of received regulatory approvals.

Years of experience.

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Latest insights from our community.

Questions and answers

Questions we think you might like answers to.

How information security is managed at EVIGROW?

EVIGROW have implemented multiple information safety measures, company information security system is ISO 27001 certified by TÜV Thüringen (Germany) for regulatory affairs, pharmacovigilance, medical writings and translation services, and complies with GDPR requirements.

What is qualification of EVIGROW personnel?

In the begining of 2025 in EVIGROW approx. 40 experts and specialists were working in regulatory affairs, pharmacovigilance, medical writings and translation fields. Majority of personnel has university degree in pharmacy or in medicine.  In addition EVIGROW has internal trainings system, in order to maintain state of the art personnel knowledge of legal, regulatory and pharmacovigilance requirements.

We have signed our first in-licensing contract, how EVIGROW can help us?

EVIGROW will identify gaps and will develop action plan for reaching marketing authorisations in target markets within shortest deadlines. This includes dossier audit/gap analysis, writing and development of missing modules and documents, eCTD compilation, submission arrangements and active support until obtaining of marketing authorisation. Providing, support with establishing pharmacovigilance system with EU QPPV office and/or local pharmacovigilance setup. After Marketing Authorisation is obtained we will continue to support through all the product lifecycle.

We are looking for the partner which can maintain our product portfolio in CEE countries, would EVIGROW support us?

EVIGROW offers regulatory affairs and pharmacovigilance services across the region, including the Baltics (Estonia, Latvia, Lithuania), Bulgaria, Czech Republic, Hungary, Poland, Romania, Slovakia, Slovenia.  Depending on Clients‘ expectations EVIGROW will seamlessly integrated with Clients‘ project management approaches and electronic regulatory and pharmacovigilance management systems.  EVIGROW has developed internal trainings library and, if needed, is able within shortest deadlines involve additional personnel into new projects.

Didn't find the answer to your question? You can always check our list of important information here or submit your question to our customer service team: info@evigrow.com

Let’s work togerther.