Regulatory Framework of Drugs in MENA: Insights

In this webinar, our experts discuss regulatory affairs of medicinal products. Two aspects that have recently gained increasing importance among the various stakeholders, namely the eCTD implementation across the region and the serialization and barcoding requirements for medicinal products.

So, we share our insights on these two aspects and share how you can avoid various issues in drug registration.

Planning your next product registration?

Let’s talk about how we can navigate eCTD and serialization to ensure smooth drug registration processes.

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Regulatory Framework of Drugs in MENA: Insights

Planning your next product registration?

Pharmacovigilance outsourcing for boosting compliance and safety for biotech companies

Breaking the Silos Across Medical Information & Pharmacovigilance – Leveraging Technology for Operational Efficiency

Whitepaper: Computerised System Validation & Pharmacovigilance

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

Clinical Research

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Quality Assurance

Regulatory Framework of Drugs in MENA: Insights

Planning your next product registration?

Pharmacovigilance outsourcing for boosting compliance and safety for biotech companies

Breaking the Silos Across Medical Information & Pharmacovigilance – Leveraging Technology for Operational Efficiency

Whitepaper: Computerised System Validation & Pharmacovigilance

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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