Webinar Archives

How to Avoid Delays in Your Early Phase Oncology Trial?

by Kamile Gruduls | Jun 10, 2022 | Clinical Research

Many things can go array in your early phase oncology trials, from protocol development, taking care of a safety profile, getting the ethics committee / regulatory authority’s approval, managing vendors, and much more. They all cost precious time and increase the...

Pharmacovigilance Opportunities in the MENA Region

by Kamile Gruduls | Jun 1, 2022 | Pharmacovigilance

Pharmacovigilance is getting more and more attention in MENA countries thanks to new regulations and steps in the right direction. The MENA region itself holds great promise for the pharmaceutical industry, being potentially hugely profitable. Together these 22...

How does the conflict between UA & RU impact the pharma industry?

by Kamile Gruduls | Mar 25, 2022 | Clinical Research, Medical Information, Pharmacovigilance, Regulatory Affairs

Like the rest of the world, the pharmaceutical and biotech industries are beginning to worry about their ability to continue operations. And with good reason. Russia’s invasion of Ukraine affects millions of people, not just in this Eastern European nation but...

Webinar: Regulatory Strategy in the EAEU and Rest of CIS Countries

by Kamile Gruduls | Mar 23, 2021 | Regulatory Affairs

Regulatory strategy in EAEU and CIS regions differ from other regions as market access to these countries can be a real challenge due to various local regulations. However, it is only a matter of experience and adequate know-how. This webinar focuses on choosing your...

Webinar: Effective IMPD Writing. The Quality Part

by Kamile Gruduls | Mar 20, 2021 | Regulatory Affairs

Effective IMPD writing, including the quality part is a vital document that contains information about an investigational medicinal product and it is an essential part of the Clinical Trial Application (CTA), which is required by competent authorities in EU. The...

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How to Avoid Delays in Your Early Phase Oncology Trial?

Pharmacovigilance Opportunities in the MENA Region

How does the conflict between UA & RU impact the pharma industry?

Webinar: Regulatory Strategy in the EAEU and Rest of CIS Countries

Webinar: Effective IMPD Writing. The Quality Part

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How to Avoid Delays in Your Early Phase Oncology Trial?

Pharmacovigilance Opportunities in the MENA Region

How does the conflict between UA & RU impact the pharma industry?

Webinar: Regulatory Strategy in the EAEU and Rest of CIS Countries

Webinar: Effective IMPD Writing. The Quality Part

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