Partnering for Success: Specialised Rescue Studies in Georgia

Discover the benefits of conducting clinical trials in Georgia through this case study of three pharmaceutical companies.

Discover how Biomapas supported three pharmaceutical companies in achieving their recruitment goals and explore the benefits of conducting clinical trials in Georgia.

With over 400 international trials, 66 active institutions, and 128 experienced Principal Investigators, Georgia is an excellent location for clinical research.

The region offers rapid patient enrolment, competitive costs, and streamlined regulatory processes, making it an attractive option for innovative treatments and high-standard medical care.

Choosing the Right QPPV Partner for EU and Global Compliance

Pharmacovigilance outsourcing has become crucial for biotech companies to remain compliant and safeguard patients. When you bring a drug to market in Europe or globally, your Qualified Person for Pharmacovigilance (QPPV) serves as your first line of defense. The right...

How to achieve Multi-Region Pharmacovigilance Compliance: Critical Lessons from CIS and MENA

Navigating local nuances can significantly impact a company’s ability to retain market access. For biotech and pharmaceutical companies, these markets are essential expansion zones with growing demand. But the path to compliance isn’t simply a matter of translating...

The use of AI/Automation in Pharmacovigilance: Ensuring Safety through Robust Processes

Artificial intelligence (AI) and automation are no longer futuristic concepts in pharmacovigilance – they are becoming operational necessities. From accelerating signal detection to improving risk-benefit assessments, tools like Veeva Systems’ AI-enabled safety...

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Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

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Partnering for Success: Specialised Rescue Studies in Georgia

Choosing the Right QPPV Partner for EU and Global Compliance

How to achieve Multi-Region Pharmacovigilance Compliance: Critical Lessons from CIS and MENA

The use of AI/Automation in Pharmacovigilance: Ensuring Safety through Robust Processes

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Big Enough To Cover All Your Needs.Small Enough To Care.

Clinical Research

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Regulatory Affairs

Medical Information

Quality Assurance

Partnering for Success: Specialised Rescue Studies in Georgia

Choosing the Right QPPV Partner for EU and Global Compliance

How to achieve Multi-Region Pharmacovigilance Compliance: Critical Lessons from CIS and MENA

The use of AI/Automation in Pharmacovigilance: Ensuring Safety through Robust Processes

Big Enough To Cover All Your Needs. Small Enough To Care.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Clinical Trials

PV System & QPPV

Post-Authorization

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Big Enough To Cover All Your Needs.
Small Enough To Care.