Innovating Healthcare,
Delivering Global Excellence.
Manufacturing high-quality pharmaceutical formulations with advanced research, global compliance, and an unwavering commitment to improving lives worldwide.
Explore Formulations by Dosage Form
Comprehensive WHO-GMP certified formulation catalog categorized by specialized dosage delivery systems.
4
WHO-GMP Plants
200+
Global Partners
150+
CTD Dossiers Ready
25+
Years of Scientific Leadership
Exporting Healthcare Solutions Across 50+ Nations
Fully registered with global health ministries, delivering EU-GMP & WHO-GMP compliant formulations with ready CTD/eCTD dossiers and temperature-controlled logistics.
Latin America (LATAM)
Key Destinations: Brazil, Colombia, Peru, Chile, Guatemala
Sub-Saharan Africa
Key Destinations: Nigeria, Kenya, Ghana, Tanzania, Uganda
Middle East & GCC
Key Destinations: UAE, Saudi Arabia, Oman, Jordan, Iraq
Southeast Asia & CIS
Key Destinations: Vietnam, Philippines, Kazakhstan, Uzbekistan
FLEMMING PHARMA
Global Product DirectoryOfficial Product Catalog & Therapeutic Dossier Index
Access detailed specifications, therapeutic categories, WHO-GMP formulation matrix, packaging configurations, and export dossier availability for over 350+ products.
Download Flemming Pharma 2026 Product Directory
Get instant access to our complete portfolio specifications, regulatory dossier list, dosage strengths, and turnkey manufacturing capabilities.
350+ Active Formulations
Solid Orals, Injectables, Cephalosporins, Eye/Ear Drops & Syrups.
Global Regulatory Matrix
Complete list of ready CTD/eCTD dossiers for 50+ export countries.
Turnkey Packaging Options
Alu-Alu, Blister, Strip, Vials, Ampoules & Bottled Suspensions.
WHO-GMP Facility Specs
Technical capabilities for Contract & 3rd Party Manufacturing.
High-Precision Therapeutic Formulations
Engineered with scientific rigor across critical healthcare categories.
Solid Oral Formulations
Film-coated tablets, sustained release capsules, and effervescent dosage forms manufactured in Cleanroom Class 100,000.
Sterile Injectables
Aseptic liquid injections, lyophilized vials, and BFS ampoules manufactured under strict ISO Class 5 sterile environments.
Cephalosporins & Anti-Infectives
Dedicated block facility ensuring zero cross-contamination for oral and injectable cephalosporins.
Cardiovascular Care
Advanced antihypertensives, statins, and antiplatelet formulations designed for long-term therapeutic adherence.
Diabetology & Metabolic
Extended release Metformin, Gliptins, and dual-action combination tablets for glycemic control.
Gastroenterology & Liquid Orals
Proton pump inhibitors, oral syrups, dry suspensions, and antacid oral emulsions.
Built on Scientific Rigor & Global Quality
WHO-GMP Facilities
State-of-the-art automated manufacturing plants adhering to international WHO-GMP and PIC/S compliance guidelines.
Advanced R & D Labs
Equipped with HPLC, Gas Chromatography, Mass Spectrometry, and reverse engineering capabilities for complex NDDS.
Dossier Support
Ready CTD and eCTD dossiers with stability data according to ICH guidelines for rapid regulatory approvals.
Global Export Reach
Active distribution and tender partnerships across Latin America, Africa, the Middle East, and Asia.
Turnkey Manufacturing
End-to-end contract manufacturing services, private labeling, and tech transfer support.
Total Quality Assurance
Zero-defect batch release protocol with 100% automated vision inspection systems.
Precision Manufacturing at Scale
Our automated manufacturing plants utilize continuous inline process monitoring, sterile isolation barrier systems, and automated vision inspection lines.
Tour Facilities5 Billion+
Annual Tablet Capacity
200 Million
Liquid Ampoules & Vials
ISO Class 5
Sterile Cleanroom Standard
100% SCADA
Automated Process Control
Certified to the Highest Global Standards
WHO-GMP
World Health Organization
ISO 9001:2015
Quality Management
ISO 14001
Environmental Safety
EU-GMP Ready
European Compliance
5-Step Quality Assurance Workflow
Inline automated testing, cleanroom isolation, and serialization at every manufacturing milestone.
Raw Material QC
NIR SpectroscopyFluid Bed Processing
High-Shear MixerRotary Tableting
Automated WeightAseptic Sterile Filling
ISO Class 5 IsolatorSerialization & QA
2D DataMatrix ReleaseRaw Material QC & Identity Verification
Every incoming API and excipient undergoes 100% identity testing using non-destructive Near-Infrared (NIR) spectroscopy inside ISO Class 7 cleanroom sampling booths.
Ready to Expand Your Pharmaceutical Supply Chain?
Connect with our international export team for contract manufacturing, dossier licensing, and distribution opportunities.