127/5 Mukono street, Mukono District
info@jalmexpharma.com
Jalmex Pharma Consultancy Opening Hours : Monday to Friday - 8 Am to 5 Pm
Help Line
+256 750 829255127/5 Mukono street, Mukono Districtinfo@jalmexpharma.comJalmex Pharma Consultancy Opening Hours : Monday to Friday - 8 Am to 5 Pm
Help Line
+256 750 829255
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.
Jalmex Pharma Consultancy provides expert support to pharmaceutical businesses seeking to strengthen compliance, quality, and operational performance. With deep industry knowledge and a practical, solution-focused approach, we help clients navigate regulatory requirements, improve systems, and build sustainable growth. Jalmex Pharma Consultancy specializes in delivering tailored pharmaceutical advisory services that support companies across the product lifecycle. Our expertise covers regulatory compliance, quality management systems, inspection readiness, audit support, and continuous quality improvement. We work closely with clients to identify gaps, reduce risk, and implement effective solutions that align with industry standards and business objectives. Whether supporting new businesses or established organizations, we provide reliable guidance that helps ensure quality, compliance, and efficiency.
- Regulatory compliance advisory.
- Quality management system development and improvement.
- Inspection readiness and audit preparation.
- Gap analysis and corrective action planning.
- Supplier and internal audit support.
- Training, coaching, and capacity building.
- Risk management and quality improvement solutions.
At Jalmex Pharma Consultancy, we combine technical expertise with a hands-on understanding of real operational challenges. Our approach is practical, collaborative, and focused on delivering measurable value to clients. We are committed to helping pharmaceutical organizations maintain high standards, meet regulatory expectations, and operate with confidence in a competitive market.
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.