EARAPA Regulatory Spotlight 4
1. What is the average medicine registration timeline in PPB, Kenya? 2. What do you advise applicants to shorten the medicine registration timeline in the kenyan system?
News
Source imageDr. Tibin Ngeiywa Anne
Regulatory Officer, Department of Product Evaluation and Registration Pharmacy and Poisons Board(PPB), Kenya has a short interview with EARAPA youtube.
Stay Tunned, it will be released soon
#SUBSCRIBE to EARAPA Official Youtube Channel
https://lnkd.in/ezdXfKQr
You can also drop a #comment for any question/s to be asked for any agency of any countries in East Africa.
We will make it as next episode of regulatory spotlights
Originally published on earapa.net
Edition 2, 27 to 29 October 2026, online
Meet regulators, manufacturers and distributors across Africa
Free for regulatory and pharma professionals.
More from EARAPA
All news- News
We are thrilled to announce our partnership with the Global Pharmaceutical Regulatory Affairs Summit
- News
National Agency for Drug Administration and control (NAFDAC) declared to be the first African Agency to achieve and sustain WHO maturity level 3 in medicine and Vaccine regulation in Africa
- News
Ghana: Food and Drugs Authority recalled over 700,000 bottles of carvedilol tablets
Next post
AMRH Steering Committee Approves Five Additional Human Medicinal Products for Continental Listing