Categories for Regulatory

Blog

Product Registration: Pro Tips for Program Managers
New contraceptive products have the potential to help women and girls plan the families and lives they desire. Among the 214 million women in developing countries with an unmet need for family planning, many cite method-related reasons for not using ... Read full article
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Overcoming Regulatory Barriers to Increase Female Condom Access
Three guest bloggers have contributed to this posting -- PATH staff members Kimberly Whipkey, Policy and Advocacy Officer, and Maggie Kilbourne-Brook, Senior Program Officer, along with Sara Semelka, Program Manager, AIDS Foundation of Chicago/Na... Read full article
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FDA Proposes Female Condom Rule Change
The U.S. Food and Drug Administration has released a proposed order to recl... Read full article
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Levoplant Receives WHO Prequalification
On June 30, 2017, the World Health Organization (WHO) prequalified Sino-implant (II), a long-acting 2-rod reversible contraceptive implant marketed globally under the name of Levoplant. This milestone is the culmination of more than a decade of comm... Read full article
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FDA to host Small Business Regulatory Conference
The U.S. Food and Drug Administration (FDA) is sponsoring a free, 2-day regulatory conference  for... Read full article
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Organisation Africaine de la Propriete Intellectuelle (OAPI)
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African Regional Intellectual Property Organization (ARIPO)
ARIPO provides an organizational structure for English-speaking African countries to pool resources, exchange information and harmonize laws and activities relating to industrial property matters. Member nations include Botswana, The Gambia, Ghana,... Read full article
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Eurasian Patent Organization (EAPO)
To perform administrative tasks relating to functioning of the Eurasian patent system and grant of Eurasian patents, the Eurasian Patent Convention (EAPC) established the Eurasian Patent Organization  (EAPO) to act as its executive body.... Read full article
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FDA Center for Drug Evaluation and Research Small Business and Industry Assistance
The U.S. Food and Drug Administration's Center for Drug Evaluation and Research (CDER) is charged with ensuring that safe and effective drugs are available to improve the health of people in the United States. CDER regulates over-the-counter and p... Read full article