Pharmacy and Poisons Board https://validator.w3.org/feed/docs/rss2.html Stakeholder Feedback Form Guidelines on submission of documentation for registration of Biotherapeutic products Guideline for submission of variation applications for registered biotherapeutic products Clinical Trials Clinical Trials Checklist and Declarations Clinical Trials Guidelines Guidelines for the conduct of good clinical practice inspections in Kenya Guidelines for the conduct of clinical trials during public health emergencies and pandemics In Kenya Guidelines for the Conduct of Clinical Trials in Kenya Side Panel Header 1 -Main Safety Alerts Building Confidence in African Traditional Medicines Strengthening Regulation of Traditional Medicine for Safer Healthcare SUPPLY AND DELIVERY OF ONE (1) NO. HIGH- PERFORMANCE THIN-LAYER CHROMATOGRAPHY (HPTLC) LABORATORY EQUIPMENT AS PER SPECIFICATIONS SUPPLY AND DELIVERY OF ONE (1) NO. LIQUID CHROMATOGRAPHY WITH TANDEM MASS SPECTROMETRY (LCMSMS) EQUIPMENT AS PER SPECIFICATIONS Blog Guidelines on submission of documentation for registration of Similar Biotherapeutic products SMPC Compendium of Guidelines on Medicines Evaluation and Registration In Kenya Guidelines on Renewal of Marketing Authorization for Medicines and Vaccines Quality Control and Lot Release Regulatory Notice : Interim arrangements for regulatory laboratory testing Guideline On Information Sharing Public Communications Policy Guideline for Lodging Complaints and Appeals at the Pharmacy and Poisons Board HPT Guidelines APPLICANT’S SCREENING CHECKLIST FOR REGISTRATION OF HUMAN VACCINES Guidelines for Good Storage and Distribution Practices for Health Products and Technologies in Kenya Guidelines for Transportation of Pharmaceuticals In Kenya Guidelines for Safe Management of Pharmaceutical Waste Guidelines for Donation of Health Products and Technologies Guidelines for Establishing Manufacturing Facilities for Health Products & Technologies In Kenya Kenya Good Manufacturing Practices Guidelines Legal Provisions, Guidelines, and Procedures Guidelines on Submission of Documentation for Emergency Use Authorization (EUA) Of Health Products And Technologies Guidelines on Submission of Documentation for Compassionate Use Authorization (CUA) of Health Products and Technologies Guideline on Evaluation And Authorisation of Unregistered Health Products and Technologies Guidelines for Suspension, Withdrawal, Withholding and Revocation of Marketing Authorization of Medical Products and Health Technologies in Kenya Guideline for Submission of Variation Applications for Registered Human Vaccines APPLICANT’S SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES (BIOTHERAPEUTIC PRODUCTS) APPLICANT’S SCREENING CHECKLIST FOR REGISTRATION OF HUMAN MEDICINES (CHEMICAL ENTITIES PRODUCTS) The Pharmacy and Poisons (Pharmacovigilance and Post Marketing Surveillance System) Rules, 2022 The Pharmacy and Poisons (Amendment) Rules, 2022 Pharmacy and Poisons (Guidelines for The Conduct of Clinical Trials), 2022 Home Guidelines on Submission of Documentation for Registration of Human Vaccines KENYA VIGILANCE MONITORING AND EVALUATION FRAMEWORK AND KEY PERFORMANCE INDICATORS (2026-2028) IMPLEMENTATION PLAN FOR ACTIVE SURVEILLANCE Pharmacovigilance