INTERNATIONAL WEBINAR ON PHARMACEUTICALS AND CLINICAL RESEARCH

November 18, 2022 | | USA

INTERNATIONAL WEBINAR
Scientex conferences are dedicated to assisting professionals in reaching their full potential by providing unique opportunities for them to explore scientific study fields to uncover and share potential breakthroughs.
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Spotlight

The FMD is due to be implemented from 09 February 2019, but in order to successfully implement the changes, companies need to be aware of the requirements and start testing their effectiveness. The new safety features will allow wholesale distributors and pharmacists to verify that the medicine is authentic, identify individual packs, and verify that the packaging has not been interfered with. Once manufacturers have met the specified requirements, they need to ensure that they are durable enough to withstand the demands of the supply chain.

OTHER LIVE WEBINARS

Strategies to Prevent and Reduce Medication Errors During Transitions of Care

September 29, 2022 | 6:00PM EST

Transitions of care (TOC) is defined as the movement from one setting of care to another. It is estimated that 60% of all medication errors occur during TOC.
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3 Keys to Creating Connected Digital Labs that Scale

October 04, 2022 |

Are data silos, reduced scientific agility and hindered collaboration keeping companies from accelerating development and delivery of new therapeutics?
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Clinical Pharmacy and Pharmacology

October 17, 2022 | 9:30AM GMT

Longdom webinars have taken a major role in this pandemic time in organizing webinars that are open for everyone, who are wishing to continue their medical/professional education without traveling.
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Regulatory & Industry Perspectives Webinar

October 18, 2022 | 5:00

The pressure points of the COVID-19 pandemic have been an unprecedented challenge for the pharmaceutical industry and generated a global spotlight on supply resiliency for drug shortage prevention.
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Spotlight

The FMD is due to be implemented from 09 February 2019, but in order to successfully implement the changes, companies need to be aware of the requirements and start testing their effectiveness. The new safety features will allow wholesale distributors and pharmacists to verify that the medicine is authentic, identify individual packs, and verify that the packaging has not been interfered with. Once manufacturers have met the specified requirements, they need to ensure that they are durable enough to withstand the demands of the supply chain.

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