Jalmex Pharma Consultancy Opening Hours : Monday to Friday - 8 Am to 5 Pm
Jalmex Pharma Consultancy offers expert pharmaceutical advisory services in regulatory compliance, quality assurance, audit support, and inspection readiness. We help businesses build robust systems, reduce risk, and achieve sustainable growth through practical, customized solutions.
End-to-End Pharmacy Establishment Solutions in Uganda
Jalmex Pharma Consultancy Limited provides comprehensive pharmacy setup services for entrepreneurs, healthcare investors, and pharmaceutical companies seeking to establish retail or wholesale pharmacy operations in Uganda. From initial business registration through NDA licensing and operational readiness, we guide you through every step of the pharmacy establishment process—ensuring full compliance with National Drug Authority (NDA) requirements and Ugandan pharmaceutical regulations.
• Company Incorporation: Registration with Uganda Registration Services Bureau (URSB) as a limited company or partnership with pharmaceutical business objectives clearly stated in Memorandum and Articles of Association.
• Pharmacist Director/Partner Integration: Structuring your company to include a registered pharmacist as a director (for companies) or partner (for partnerships) as required by NDA regulations.
• Tax Registration: Obtaining Tax Identification Number (TIN) from Uganda Revenue Authority (URA).
• Trading License: Securing local trading license from municipal authorities. Premises Selection and Suitability Assessment Location and premises suitability are critical factors in NDA's approval process. We assist with:
• Site Selection Guidance: Identifying suitable premises considering NDA's distance requirements from existing pharmacies (like-to-like measurement: retail-to-retail, wholesale-to-wholesale, human-to-human, veterinary-to-veterinary).
• Premises Suitability Assessment: Evaluating proposed locations against NDA's minimum standards for floor area, layout, storage capacity, and operational requirements.
• Location Approval Application: Submitting applications for NDA's approval of proposed pharmacy location—valid for 3 months with one extension possible upon justified request
• Sketch Plan Development: Preparing detailed premises layout plans showing minimum floor areas for retail/wholesale operations, storage areas, dispensing counters, and customer service zones.
• Completion of NDA application forms for Certificate of Suitability.
• Preparation of site master plans and premises sketch plans meeting NDA specifications.
• Compilation of supporting documents including certificate of incorporation, Form 20 (director appointments), TIN certificate, and memorandum/articles of association.
• Online submission through NDA Management Information System (NDAMIS) platform.
• Guidance on premises setup to meet NDA's minimum standards before inspection.
• Review of facilities against Part III (wholesale) or Part IV (retail) requirements of Certificate of Suitability Regulations.
• Signpost installation guidance displaying NDA location approval and intended business type
• Scheduling and coordination of NDA premises inspection.
• Pre-inspection readiness assessment and gap identification.
• Representation during NDA inspector visits.
• Response to any inspection queries or corrective action requests.
• Duly filled NDA license application forms.
• Certified copies of supervising pharmacist's certificate of registration with Pharmaceutical Society of Uganda (PSU).
• Valid PSU annual membership certificate for supervising pharmacist.
• Commitment letters from supervising pharmacist specifying time and duration of physical presence at the premises.
• List of auxiliary pharmacy staff with identification details, qualifications, and registration certificates.
• Commitment letters from auxiliary staff.
• Evidence of prescribed fee payment through NDA's online payment system.
• Assistance identifying and engaging qualified, registered pharmacists resident in Uganda.
• Verification of pharmacist credentials and PSU registration status.
• Guidance on pharmacist employment terms and commitment letter requirements.
• Support for pharmacist director/partner integration into company structure.
• Guidance on recruiting qualified pharmacy auxiliary staff (pharmacy technicians, dispensers).
• Verification of auxiliary staff registration with relevant professional councils.
• Documentation of auxiliary staff qualifications and commitment letters.
• Warehouse Design: Layout optimization for proper stock rotation, temperature control, and segregation of different product categories.
• Storage Conditions: Implementation of temperature monitoring systems, cold chain facilities where required, and protection from light, moisture, and contamination.
• Distribution Controls: Development of procedures for order processing, picking, packing, dispatch, and transportation.
• Documentation Systems: Batch tracking, expiry management, recall procedures, and distribution records.
• Personnel Training: GDP training for warehouse and distribution staff.
• Engagement of qualified veterinary professionals (Veterinary Surgeons) as supervising personnel.
• Segregation of human and veterinary medicine sections where both are offered.
• Compliance with veterinary-specific storage and handling requirements
• Coordination with relevant veterinary regulatory bodies
• Assessment of location eligibility for dual operations
• Separate supervision arrangements with dedicated pharmacists for each section.
• Physical segregation of retail and wholesale operations within the same premises
• Compliance with minimum requirements for both outlet types
• Documentation demonstrating institutional embedding and patient-serving purpose
• Compliance with institutional pharmacy-specific requirements
• Integration with facility licensing and healthcare service approvals
1. Initial Consultation: Understanding your business objectives, investment capacity, and target market.
2. Business Structure Advisory: Recommending optimal legal structure (company vs. partnership).
3. Pharmacist Engagement: Identifying and engaging a qualified supervising pharmacist.
4. Premises Search: Assisting with identification of suitable locations meeting NDA distance requirements. Phase 2: Business Registration (Weeks 2-4)
5. Company Incorporation: URSB registration with pharmaceutical objectives.
6. Tax Registration: URA TIN acquisition.
7. Trading License: Municipal trading license procurement.
8. Bank Account Setup: Corporate banking arrangements Phase 3: Premises Approval (Weeks 4-8)
9. Location Approval Application: Submission to NDA for proposed location approval.
10. Site Plan Development: Preparation of detailed premises layout.
11. Location Approval: NDA review and approval (valid for 3 months)
12. Signpost Installation: Display of NDA approval notice at premises Phase 4: Certificate of Suitability (Weeks 8-12)
13. Premises Setup: Organizing premises according to NDA minimum standards.
14. Suitability Application: NDAMIS submission with all required documents.
15. Pre-Inspection Readiness: Final preparations and gap closure.
16. NDA Inspection: Coordination of premises inspection.
17. Certificate Issuance: Receipt of Certificate of Suitability of Premises. Phase 5: Operating License (Weeks 12-16)
18. License Application: NDAMIS submission with complete documentation.
19. Fee Payment: Online payment of prescribed license fees.
20. License Inspection: NDA inspector allocation and visit.
21. License Issuance: Receipt of pharmacy operating license and premise number.
22. Operational Launch: Pharmacy commences operations.
Total Timeline: Approximately 3-4 months from initiation to operational license, depending on premises readiness and NDA processing times.
• Kampala Central Division: UGX 1,060,000
• Kampala Other Divisions: UGX 645,000
• Outside Kampala (Municipal): UGX 276,000
• Outside Kampala (Rural): UGX 276,000
• Kampala Central Division: UGX 660,000
• Kampala Other Divisions: UGX 420,000
• Outside Kampala (Municipal/Rural): UGX 156,000
• Preparation and submission of annual Return of Details of Pharmacy Business forms to NDA by January 31st each year.
• Updates on any alterations to pharmacy particulars within 21 days of changes.
• Renewal applications submitted at least 3 months before license expiry (licenses valid for 3 calendar years).
• Coordination of renewal inspections and documentation updates.
• Change of Supervising Pharmacist: Documentation updates and NDA notifications.
• Change of Ownership: Sale agreements, board resolutions, and new license applications.
• Relocation: Prior written approval applications and distance compliance verification.
• Upgrade from Retail to Wholesale: License conversion applications meeting wholesale requirements.
• Implementation of NDA procedures for destruction of expired drugs.
• Certificate of destruction documentation for license renewals.
• Ongoing advisory on evolving NDA guidelines and pharmaceutical regulations.
• Training on new compliance requirements and best practices
✓ Business structure advisory and company incorporation support.
✓ URA TIN registration and trading license coordination.
✓ Premises suitability assessment and location approval applications.
✓ Site master plan and sketch plan development.
✓ Complete Certificate of Suitability application management.
✓ NDA inspection preparation and coordination.
✓ Operating license application and documentation.
✓ Pharmacist recruitment and engagement support.
✓ Auxiliary staff documentation and compliance.
✓ NDAMIS platform registration and online submission.
✓ Fee payment guidance and processing support.
✓ License collection and handover.
✓ Post-license compliance advisory and annual returns support.
• Assessment of your business objectives and investment capacity.
• Overview of regulatory requirements and timeline expectations.
• Preliminary premises suitability guidance.
• Fee structure explanation (regulatory fees + professional fees)
• Customized pharmacy setup roadmap.
Jalmex Pharma Consultancy Limited.
Your Trusted Partner in Pharmacy Establishment Kampala, Uganda
Gain practical experience in pharmaceutical product formulation in Uganda, from pre-formulation and prototype design to scale-up, bioequivalence studies, regulatory approval, and commercialization.
We bridge APIs with excipients to develop stable, effective dosage forms like tablets, capsules, creams, and lotions—optimized for patient needs and market success.
Simplify drug registration in Uganda with our dossier preparation in CTD format for submission to the National Drug Authority (NDA).
We ensure smooth approval and ongoing retention on the national drug register, helping your products launch faster.A registered pharmacist in Uganda and an experienced Industrial Pharmacist with over 7 years of expertise in pharmaceutical manufacturing. She graduated with a Bachelor's Degree in Pharmacy from Istanbul University, bringing strong technical knowledge to Jalmex Pharma Consultancy Limited.
Core Competencies
Dr. Amuge specializes in:
GMP compliance (Good Manufacturing Practice)
Quality Assurance (QA) & Quality Management Systems (QMS)
Production operations in pharmaceutical manufacturing
Regulatory support* for pharmaceutical manufacturers
Operational efficiency and product quality improvement Professional Impact She helps pharmaceutical manufacturers in Uganda and East Africa *enhance operational efficiency, elevate product quality, and maintain compliance with industry standards* including NDA, WHO, and international pharmaceutical requirements.
Anthony Aheebwa is a pharmacist and pharmaceutical quality professional based in Uganda, specializing in industrial pharmacy practice, regulatory affairs, and pharmaceutical quality systems. With extensive experience in Good Manufacturing Practice (GMP) implementation, he leads quality assurance and regulatory compliance initiatives across Uganda’s pharmaceutical sector.
Anthony’s expertise includes GMP-compliant quality systems, batch release oversight, document control, CAPA (corrective and preventive actions) management, risk assessment, self-inspections, and regulatory submissions.
He has supported multiple product pre-market authorizations and registrations with the National Drug Authority (NDA) and has played a pivotal role in strengthening operational and quality systems within pharmaceutical manufacturing environments. Trusted for delivering compliance-driven solutions, Anthony helps manufacturers meet regulatory requirements, improve product quality, and maintain continuous GMP compliance.
Muhamudu Lugolobi is an experienced pharmaceutical chemist with over 10 years in pharmaceutical manufacturing, specializing in technology transfer, process scale-up, and production operations. He leads the transition of products from research and development into commercial manufacturing, ensuring efficient production, consistent product quality, and full regulatory compliance. Core expertise: Technology transfer and process scale-up for commercial pharmaceutical production GMP-compliant manufacturing and quality assurance Troubleshooting and optimizing large-scale production operations Ensuring lab formulations are manufacturable at scale without compromising safety or performance Regulatory compliance and documentation for manufacturing readiness Muhamudu delivers practical manufacturing solutions that reduce time-to-market, improve yield, and maintain regulatory standards. Ideal for pharmaceutical companies seeking a seasoned professional to manage commercialization, scale-up projects, and operational excellence.