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8 February 2013
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The US Food and Drug Administration (FDA) has announced that it is collecting comments from industry in advance of a March 2013 meeting that will decide whether gamma-Hydroxybutyric acid (GHB), an
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Regulatory Update
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12 November 2012
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Together with the World Health Organization (WHO) and the Pan American Health Organization (PAHO), Brazil's National Health Surveillance Agency (Anvisa) recently hosted two international meetings on
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28 August 2012
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An advocacy group wants to know why a South African provincehealth department is continuing to use a male circumcision clamp not approvedby the World Health Organization (WHO).A report in The NewAge
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23 July 2012
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New guidance issued by the World Health Organization (WHO) is intended to aid countries in assessing pre-exposure prophylaxis (PrEP) drugs for use in preventing the transmission of HIV in high-risk
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Regulatory Update
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21 May 2012
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Numerous regulatory agencies met on 18 May in Geneva, Switzerland to discuss whether it is possible to find new ways to allow their drug regulatory bodies to cooperate.The meeting, an international
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15 May 2012
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A new program announced by the US Food and Drug Administration aims to strengthen global regulatory capacity by working with the World Health Organization (WHO) to support new, innovative approaches
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15 May 2012
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A new paper exploring counterfeit and substandard medicines shows the presence of even a minimally-developed regulatory program can have a profound impact on ensuring consumers have access to genuine,
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12 April 2012
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International healthcare bodies are looking to issue guidelines on ‘dual use’ research on potentially hazardous materials and diseases after a researcher sent shockwaves through the medical community
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4 April 2012
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An active pharmaceutical ingredient (API) inspection program involving many of the world’s premiere global regulatory bodies announced recently its intent to standardize the inspection schemes of the
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3 April 2012
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A new United Nations-backed initiative aims to give Africans consistent access to “essential, high quality, safe and affordable medicines” through the establishment of regulatory harmonization and
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