WHO-GMP & ISO 9001:2015 Certified Contract Manufacturing

WHO-GMP Third Party Pharmaceutical Manufacturing in India

Accelerate your brand with Riomedica Healthcare Pvt. Ltd. We offer comprehensive third-party contract manufacturing across India for Tablets, Capsules, Injectables, Oral Liquids, and Derma products. Backed by India's top manufacturing plants, DCGI approvals, and rigorous batch quality assurance.

Production at India's Top WHO-GMP Plants
700+ DCGI Approved Formulations
High Quality ALU-ALU & Blister Packing
100% Certificate of Analysis (COA)
Rapid Turnaround: 25-35 Days Dispatch
Complete Foil Artwork & Packaging Design
Manufactured at India's Top Certified Plants:
Akums Drugs Windlas Biotech Biodeal Pharma Medicef Pharma Mascot Health Series

Request Contract Quotation

Share your formulation requirement. Our technical team responds within 4 business hours.

700+
DCGI Approved Formulations
25-35
Days Delivery Timeline
100%
Batch Quality Lab Tested
6+
WHO-GMP Plants Partnered
Manufacturing Capabilities

Comprehensive Contract Manufacturing Across All Dosage Forms

State-of-the-art automated machinery, strict climate controls, and high-speed packaging lines for pharmaceutical leaders across India.

Tablets Section

High-speed rotary compression machines producing uncoated, film-coated, enteric-coated, sustained release, bilayered, and effervescent formulations.

ALU-ALU Blister Beta-Lactam Non-Beta

Capsules Section

Automatic capsule filling lines handling size 00 to 4 hard gelatin capsules and modern soft gelatin encapsulation for vitamins, oils, and minerals.

Hard Gelatin Softgel Pellet Filling

Injectables (Dry & Liquid)

Class 100 laminar airflow cleanrooms for sterile liquid ampoules, vials, lyophilized powders, cephalosporins, and carbapenem dry injections.

Dry Powder Vials Liquid Ampoules Sterile WFI

Oral Liquids & Syrups

Automated bottle washing, volumetric liquid filling, measuring cap sealing, and tamper-evident labeling for cough syrups, multivitamins, and pediatric suspensions.

Amber PET Suspensions Pediatric Drops

Derma Ointments & Creams

Vacuum planetary mixers and automated tube filling for antifungal creams, corticosteroid ointments, medicated soaps, lotions, and sunscreens.

Lami Tubes Aluminium Tubes Topical Gels

Nutraceuticals & Sachets

FSSAI approved modern powder blending, stick pack and three-side seal sachet packaging for energy drinks, pre-probiotics, collagen, and protein powders.

Sachets HDPE Jars Energy Drinks
Streamlined Execution

5-Step Seamless Third Party Manufacturing Workflow

From formulation finalization to finished dispatch, our regulatory and operations team ensures complete transparency.

1

Formulation Selection

Select your composition from our 700+ DCGI approved list or provide your custom formula.

2

Contract Quotation

Transparent cost breakdown covering raw materials, excipients, foil printing, cartons, and conversion.

3

Artwork Approval

In-house design team produces 3D box mockups and ALU foil artwork complying with Schedule M regulations.

4

Batch Production

Manufacturing in certified WHO-GMP plants with strict in-process quality controls and stability testing.

5

Dispatch with COA

Delivery via insured road transport with signed Certificate of Analysis and laboratory assay reports.

Have an Immediate Manufacturing Requirement?

Connect with our Contract Manufacturing Director for fast pricing and slot reservation.

Frequently Asked Questions

Answers to Contract Manufacturing Queries

Clear answers regarding MOQs, timelines, regulatory approvals, and packaging.

What are the standard Minimum Order Quantities (MOQs)?
Our standard minimum order quantities are designed for feasibility: Tablets (50,000 to 1,00,000 tablets), Capsules (30,000 to 50,000 capsules), Liquid Injections (2,500 to 5,000 vials/ampoules), Oral Liquids (2,000 to 5,000 bottles), and Derma Ointments (3,000 to 5,000 tubes). Customized batch sizes can be evaluated based on the active ingredient value.
What is the delivery turnaround time for new contract orders?
For new brand launches, manufacturing takes approximately 30 to 40 days to account for packaging artwork approval, foil cylinder engraving, and batch analysis. For repeat batches, delivery is streamlined to 20 to 25 days from invoice confirmation.
Which documents are required from my side?
You will need to provide: 1) Wholesale Drug License copy (Form 20B/21B), 2) GST Registration Certificate, 3) Company PAN Card, 4) Trademark registration certificate or TM application copy for your brand name, and 5) Standard non-encumbrance undertaking.
Do you assist with brand artwork and foil design?
Yes. We provide end-to-end design assistance. Our regulatory team ensures that all carton and blister foil artworks feature correct statutory warnings, composition labeling, storage conditions, barcoding, and manufacturer details as per Indian CDSCO guidelines.
Is every batch tested before dispatch?
Absolutely. Every single manufacturing batch undergoes stringent physicochemical, microbiological, and assay testing. Finished consignments are released strictly with an authorized Certificate of Analysis (COA) confirming 100% pharmacopoeial compliance.