Turnkey Private Label Softgel Manufacturing in Pakistan
From proprietary formula R&D and pharmaceutical cGMP encapsulation to customized packaging, stability testing, and DRAP compliance — build a high-margin, scalable supplement brand with Elate Pharma.
Certified Quality Standards
QC Status
Approved
Batch #EP0526
PassPrivate Label Ready
Bulk Supply Capacity
QC Process
Karachi, Pakistan
Softgel Product Line
Manufacturing Facility
Complete End-to-End Private Label Solutions
We manage the complex pharmaceutical chemistry, encapsulation engineering, and secondary packaging under one roof so you can focus entirely on retail detailing, marketing, and brand growth.
Custom Formulation & R&D
Our formulation pharmacists engineer bespoke active ingredient blends including oily solutions, suspensions, emulsions, and fat-soluble nutrient matrices using USP/BP-grade actives.
Gelatin Shell Engineering
Certified Halal bovine gelatin shells available in custom transparent, opaque, or pearlescent colors with oval, oblong, round, and enteric-coated acid-resistant dies.
cGMP Precision Encapsulation
State-of-the-art automated rotary die encapsulation lines located in Class D/C HVAC cleanrooms ensure uniform micro-dosing with less than 1.5% fill variation.
In-House Laboratory & QC
Every production batch undergoes comprehensive HPLC assay verification, microbial limit testing, heavy metal screening, and dissolution testing before COA release.
Turnkey Packaging & Labeling
Complete secondary packaging solutions including pharmaceutical HDPE amber bottles, heat-induction tamper seals, blister packs, and premium unit cartons with spot UV and embossing.
Regulatory & DRAP Guidance
Comprehensive regulatory documentation support for DRAP Form-7 product enlistment, stability study dossiers, and statutory label compliance.
High-Growth Private Label Formulation Pathways
Leverage market-tested active ingredient matrices across beauty, longevity, brain health, and specialized wellness categories.
Beauty & Nutricosmetics
High-demand glow and anti-aging formulations built for modern skincare and wellness consumers.
Key Formulations:
- •Reduced L-Glutathione (500mg)
- •Marine Collagen Peptides Complex
- •Cold-Pressed Evening Primrose Oil (1000mg)
- •Biotin + Zinc High-Potency Matrix
Cardiovascular & Daily Vitality
Therapeutic lipid and co-factor formulations supporting heart health, energy, and cellular function.
Key Formulations:
- •Triple-Strength Omega-3 (18/12 & 36/24)
- •Coenzyme Q10 (100mg) with Vitamin E
- •Vitamin D3 (5000 IU) + K2 (MK-7)
- •Bioavailable Magnesium Complex
Cognitive & Vision Support
Targeted carotenoid and herbal extracts designed for digital eye fatigue and mental clarity.
Key Formulations:
- •Eye Defense Lutein (20mg) + Zeaxanthin
- •Standardized Ginkgo Biloba (120mg)
- •High-DHA Phospholipid Complex
- •Astaxanthin Antioxidant Shield
Men’s & Women’s Targeted Health
Clinically backed botanical blends addressing hormone balance, prostate comfort, and vitality.
Key Formulations:
- •Saw Palmetto Prostate Complex
- •Prenatal L-Methylfolate + B12
- •Organic Moringa Oleifera (500mg)
- •Zinc Picolinate Cellular Support
The 6-Step Private Label Manufacturing Roadmap
A transparent, structured development pipeline engineered for predictable timelines, zero production surprises, and on-time market launch.
Formulation Consultation
Define your target health indication, active ingredient strengths, dosage forms, bottle counts, and market price targets.
R&D Pilot Batch & Lab Testing
Our laboratory produces test samples to verify active solubility, gelatin ribbon viscosity, and dissolution rates.
Packaging & Label Artwork Approval
Review bottle specifications, induction seal types, and audit label copy against DRAP statutory requirements.
cGMP Mass Encapsulation
Full-scale encapsulation in cleanrooms followed by multi-stage dehumidification drying tunnels.
QC Testing & Batch COA Release
Stringent analytical assay, microbial limits, and heavy metal testing with signed Certificate of Analysis.
Finishing & Commercial Dispatch
High-speed automated bottling, induction sealing, labeling, and carton packing ready for retail distribution.
Packaging Options Engineered for Pharmacy Shelves & D2C Unboxing
We offer comprehensive secondary packaging so your finished product is 100% shelf-ready upon arrival.
HDPE Amber Bottles
Pharmaceutical 60cc to 250cc bottles with child-resistant caps (CRC) and airtight heat-induction foil wads.
Alu-Alu & PVC Blisters
10-count and 15-count push-through blister packs offering maximum individual unit barrier protection against humidity.
Premium Retail Unit Cartons
Custom SBS paperboard cartons with metallic foil stamping, soft-touch matte lamination, and spot UV varnishes.
Frequently Asked Questions (FAQ)
Clear, direct answers regarding private label softgel contract manufacturing in Pakistan.
Q.What is the minimum order quantity (MOQ) for private label softgel manufacturing?
Our private label softgel packaging runs typically start at 2,000 to 3,000 finished bottled units for standard formulations, or 100,000 loose softgels for custom bulk production. We offer pilot run flexibility to help emerging brands establish their market footprint responsibly.
Q.Can we provide our own custom formula, or does Elate Pharma develop it?
Both! If you have an established formulation, our technical team will review it for softgel encapsulation feasibility, viscosity, and stability. Alternatively, our R&D pharmacists can custom-formulate a bespoke blend tailored to your target therapeutic claims and marketing goals.
Q.What regulatory support do you provide for DRAP enlistment in Pakistan?
As a licensed, DRAP-enlisted pharmaceutical manufacturing facility (Form-6), we provide complete technical dossiers including Finished Product Specifications (FPS), Certificate of Analysis (COA), Master Formula Records (MFR), and stability study summaries required for your Form-7 product enlistment.
Q.How long does the private label development and production cycle take?
A standard initial private label run typically takes 6 to 8 weeks from final formulation and artwork sign-off to finished product dispatch. Reorders on approved formulas move through a streamlined 3 to 4 week production schedule.
Q.Who owns the product formula and intellectual property?
You maintain 100% ownership of your proprietary brand name, trademarks, packaging designs, and commercial marketing rights. We operate under strict non-disclosure agreements (NDAs) to protect your brand assets.
Ready to Build Your Private Label Supplement Line?
Schedule a direct technical consultation with our formulation pharmacists and manufacturing specialists.
Private label + bulk supply path
Formula, label, packaging, MOQ, and dispatch guidance in one inquiry flow.