Contract Manufacturing
WHO-GMP Certified Formulations & Custom Manufacturing Solutions
Flemming Pharma provides WHO-GMP quality for all formulation requirements. As a reliable and trusted partner of healthcare industries worldwide, we manufacture products on a contract basis at our state-of-the-art facilities for leading pharmaceutical companies across domestic and export markets. Backed by a team of highly qualified and experienced technical professionals, we customize the full range of pharma formulations as per customer specifications.
Salient Features & Capabilities:
Supported Dosage Capabilities:
3rd Party Manufacturing Workflow
3rd Party Manufacturing
Turnkey Private Labeling & Third-Party Pharmaceutical Production
Flemming Pharma offers WHO-GMP compliant pharmaceutical medicines through Third Party Manufacturing in India for international clients and domestic brand partners. Our large-scale production capacity and qualified technical staff are a perfect combination for sufficing all your third-party manufacturing requirements under private labeling. We maintain stringent quality standards at all stages of production, starting from raw material procurement, process optimization, formulation, testing, and final export packaging.
With our commitment towards working collaboratively with customers, we provide Quality Branded medicines and Generics worldwide. It has been one of our most valuable and esteemed services to clients around the globe.
Institutional Tenders
Government Supply Contracts & Fast-Track Emergency Tenders
As per the World Health Organization (WHO), efficient medicine supply systems are a necessity for a strong healthcare system in any country. Sustainable financing, adequate human resources, comprehensive information systems, and seamless coordination between healthcare partners and institutions are key components to ensure uninterrupted availability of essential medicines.
Flemming Pharma collaborates with government health ministries, public health bodies, and community hospital networks to supply essential medicines, improving regional healthcare indices. Apart from long-term supply tenders, we also cater to urgent demand for emergency tenders where we fast-track the dispatch process to meet critical deadlines.
Tender Execution Highlights
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WHO Essential Medicines List (EML)Formulations adhering strictly to WHO guidelines.
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Cold Chain & Temperature LogisticsMonitored 2-8°C cold chain shipping for biologicals.
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Full Regulatory Certificate PackageCOPP, GMP certificate, COA, and FSC documentation.
Generic Medicines
Comprehensive Portfolio of High-Quality Bioequivalent Generics
Flemming Pharma is a leading Generic Pharmaceutical company, manufacturing bioequivalent generic medicines and building a formidable presence across emerging and regulated markets globally. Our generic formulations cover every major therapeutic category and an extensive range of dosage forms. With our deep customer relationships, quality medicines, and consistently delivered promise, we are a globally trusted brand for generic healthcare.
Major Therapeutic Classes Covered
Comprehensive Dosage Forms
OTC Products
Dedicated Consumer Healthcare & Over-The-Counter Division
Flemming Pharma has extended its formulation capabilities into Over-The-Counter (OTC) medicines and established a dedicated independent unit to manage consumer healthcare formulations. Following major success in pain management products, the company has rapidly expanded into other fast-growing OTC categories including cough syrups, nutritional health products, gastro digestive preparations, protein supplements, clinical skincare, and personal care formulations.
Our target distribution channels span Retail Pharmacies, Health and Cosmetic Chains, Drugstores, and Lifestyle Wellness Spas across international markets.
Global Retail Distribution
Our OTC products are packaged in consumer-friendly, vibrant, compliant packaging designed for retail shelves and international pharmacy networks.
- Custom private label design & packaging
- Multi-language labeling (English, French, Spanish, Arabic)
- Barcode & GS1 serialization compliant
- Fast turnaround and flexible order quantities
Drug Regulatory Affairs (DRA) Scope
Registration Services
- • DMF (CTD & eCTD format) Preparation, Review & Submission
- • Comprehensive Dossier Writing & Technical Review
- • Country-Specific Dossier Registration Filings
Post-Approval Changes
- • Product Re-Registration & Maintenance
- • Site License Renewals as per Scheduled Timelines
- • Post-Approval Product Lifecycle Management
Pre-Registration Services
- • Drug Product DMF Development & Compilation
- • Technical Document Creation & Content Management
- • Bioequivalence Study Protocols & Analytical Validation
Regulatory Service
Global Regulatory Strategy, CTD/eCTD Dossiers & Marketing Approvals
Entry into international pharmaceutical markets requires thorough understanding of complex regulatory requirements. At Flemming Pharma, our Drug Regulatory Affairs (DRA) specialists assist clients in planning and managing their pharmaceutical product development programs and regulatory filings. We ease the process of obtaining swift marketing approvals by defining country-specific regulatory strategies from the nascent stage of product development and eliminating potential roadblocks en-route to a successful product launch.
Quality Control & Quality Assurance (QC / QA)
State-of-the-Art Analytical Laboratories & Stringent Quality Management Systems
Flemming Pharma maintains strict quality standards to meet global regulatory expectations. Implementation of our Quality Policy is driven through an integrated Quality Management System (QMS) based on firm adherence to current Good Manufacturing Practices (GMP & cGMP) in conformance with national and international regulatory standards such as WHO, FDA, and ISO 9001.
Quality Assurance (QA)
Comprehensive environmental monitoring, equipment calibration, and process validation programs from raw material procurement to finished batch release. SOP guidelines govern every manufacturing and analytical procedure.
Quality Control (QC) Labs
Separate specialized testing areas for Raw Materials, Instrumental Analysis, Microbiology, Sterility, and Packaging. Equipped with HPLC, GLC, UV-Vis Spectrophotometers, FTIR, and Dissolution testers per GLP standards.
Lab Instrumentation
- High Performance Liquid Chromatography (HPLC)
- Gas-Liquid Chromatography (GLC)
- UV-Visible Spectrophotometers
- Fourier Transform Infrared Spectroscopy (FTIR)
- Atomic Absorption Spectrophotometers
- Automated Dissolution & Disintegration Testers
- Sterile Class 100 Laminar Air Flow Clean Booths