Ensure safety and compliance with adverse event monitoring

With our adverse event (AE) monitoring services, you can detect, assess, and prevent adverse events or reactions in your pharmaceutical trials. With a global presence and 24/7 support, we extend our AE monitoring expertise in more than 150 languages. Pursue your medical research, assured of your adherence to regulatory standards. Book a free consultation today and elevate your work to its highest quality.

We’ve worked with

Ipsos, Kantar, Netflix, TikTok, and Microsoft logo
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Why our adverse event monitoring service stands out?

The world of medical products and pharmaceuticals is rife with potential risks. Even with rigorous testing, unforeseen adverse events can occur. It’s not just about detecting these events but understanding, managing, and preventing them that makes the difference. We offer AE monitoring across the globe, offering 24/7 support in over 150 languages.

Responsive detection and alerting

We detect adverse events as they happen, allowing for immediate action. We alert you in time to send reports within regulatory requirement times.

Regulatory compliance assurance

With ever-evolving regulations in the healthcare sector, staying compliant is a challenge. We train our team to align with global regulatory standards, ensuring you’re up-to-date and always on top of your trial requirements. We are also BHBIA certified in AE Reporting for Market research.

Custom solutions for diverse needs

No matter your medical industry niche, we tailor our services to your unique needs and challenges. We can handle and scale your team to your evolving project requirements.

Why choose Global Lingo for your AE monitoring needs?

Comprehensive coverage

From drugs and biologics to medical devices and cosmetics, our monitoring covers a wide range of products, ensuring comprehensive safety surveillance.

Data security and confidentiality

As an ISO 27001-certified entity, we guarantee your data’s utmost security and confidentiality, ensuring patient privacy and regulatory compliance.

Swift response mechanism

Time is critical when it comes to adverse events. Our rapid response infrastructure ensures timely interventions, minimising risks and potential damages.

Cost-effective solutions

Ensuring safety doesn’t have to be a financial burden. Our competitive pricing ensures you get top-tier monitoring services without straining your budget.

Dedicated ongoing support

Our commitment doesn’t end with monitoring. We offer dedicated support and additional services, guiding you through the complexities of adverse event management and regulatory compliance.

Our client onboarding process

How do our adverse event monitoring services work?

Step 1

Start with an initial consultation

We begin with a comprehensive consultation where we understand your products, target demographics, and specific monitoring needs. We’ll then connect you with dedicated project and account managers for a streamlined experience.

Step 2

Get matched with your perfect team

We’ll partner you with your optimal adverse event team, setting up custom monitoring procedures and protocols. Rest assured that your medical trial will have comprehensive coverage and detection.

Step 3

Continuous analysis and support

Our experts continuously analyse your data, providing regular insights and recommendations for informed decision-making. You’ll have the tools you need to hit all your reporting deadlines.

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Guaranteed confidentiality and security for any sized project

We can provide a secure, impartial and confidential service. We are ISO 9001 (quality management) and ISO 27001 (information security) certified, underpinning our goal to strive for the highest quality of work produced.

Don’t just hear it from us.
Listen to what our clients have to say…

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Adverse event monitoring FAQs

Our ISO 9001 certification underlines our commitment to quality. We employ advanced tools and expert analysts to ensure accurate and timely detection of adverse events.

Patient confidentiality is our top priority. Being ISO 27001-certified, we adhere to stringent data protection standards, ensuring all patient data remains secure and confidential.

Absolutely. We understand that every product and target demographic has its unique challenges. We tailor our monitoring protocols accordingly to ensure comprehensive coverage.

We stay ahead of global regulatory changes and update our protocols accordingly. With us, you can be confident of always staying compliant, irrespective of regulatory shifts.