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.
At Jalmex Pharma Consultancy (“we,” “us,” “our”), we are committed to protecting your privacy and ensuring the security of your personal information. This Privacy Statement explains how we collect, use, disclose, and safeguard your data when you visit our website or engage with our services.
• Email: pharma@jalmexpharma.com
• Address: Mukono
• Phone: +256 750 829255
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Jalmex Pharma Consultancy
Email: info@jalmexpharma.com
Address: Mukono
Phone: +256 750 829255
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.