Ph.D. in Pharmaceutical Sciences
B.A. in Biology and Chemistry
Loice Kikwai, Ph.D, DBA LCK Pharmaceutical Consulting is has extensive experience in the field of pharmaceutical medicines regulation and standardization.
We provide consulting services on global pharmaceutical best practices for Medicines Regulatory Agencies (MRAs), pharmaceutical companies and contract research organizations (CROs) to ensure development, manufacturing, and registration of safe, effective, and high-quality medicines.
We offer advisory and training services related to
compendial methodology, compendial procedures, general chapters and guidelines for testing of medicines, particularly in the area of generics products.
Performs consultations, training, audits, and projects for National Regulatory Authorities and Pharmaceutical organizations in various countries including Ghana, Saudi Arabia, Bahrain, Kuwait, Rwanda, Angola, Eritrea, South Africa, UAE, ASEAN region countries, India, Jordan, Egypt, Oman, Ethiopia, Turkey, and Botswana.
Serves as an invited and returning speaker at various global conferences to promote and strengthen regulations for the safety, efficacy, and quality of generic pharmaceutical drug products.
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