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Monthly Archives: September 2014

New FDA draft guidance risks ‘Confused Consent’

Clinical trials require researchers to ensure that each participant is fully aware of the details of the trial before they take part. The FDA’s recently released draft guidance for Institutional Review Boards (IRBs), clinical investigators and sponsors on Informed Consent … Continue reading

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2014 ARCS scientific congress: New Guidelines for Evidence for Listed Medicine Claims

The TGA has released new Guidelines for Evidence for claims for listed medicines on the Australian Register of Therapeutic Goods (ARTG). Narelle Loewy, our Complementary Medicines expert, has summarised the changes for you in this easy reference synopsis. Click on … Continue reading

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2014 ARCS scientific congress: Naming biosimilar medicines – are we any closer?

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2014 ARCS scientific congress: ethics in HTA and decision-making

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2014 ARCS Scientific Congress: Plenary Session Day One

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commercial eyes recruiting: medical information consultant

Due to ongoing demands in our Medical Services department, we are looking for a Medical Information Consultant who has a Bachelor of Pharmacy or a related discipline, and at least 3 years experience providing drug information to Healthcare professionals and … Continue reading

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7 ways to give your Prescription Medicine Registration submission the best chance of success

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top 5 essentials to a seamless medical information transition

Partnering with a Medical Information services provider is a great way for you to focus your limited resources on key areas of your business. However, it’s important to give due consideration – as early as possible – to how the … Continue reading

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