B2B Manufacturing Partner

Your Trusted Contract Manufacturing Partner

GMP-certified · Custom formulations · Scalable capacity

Discuss Requirements
WHO-GMP
ISO 9001:2015
DCGI Approved
FSSAI Certified
GLP Compliant
cGMP Standard
Our Expertise

Comprehensive Manufacturing Capabilities

We offer end-to-end contract manufacturing solutions across a wide range of therapeutic segments and dosage forms.

Tablet & Capsule Mfg

High-speed rotary presses and fully automated capsule filling lines.

Liquid Formulations

Sterile automated filling and sealing for syrups, suspensions, and drops.

Injectable Manufacturing

Class 100 aseptic filling zones for liquid and dry powder injectables.

Topicals

Advanced homogenizers for creams, ointments, and gels.

Custom Packaging

Alu-Alu, blister, strip packaging, and automated cartoners.

API Sourcing

Reliable global procurement of high-quality active pharmaceutical ingredients.

3

Manufacturing Plants

500M+

Tablets / Year

50+

Production Lines

100%

In-house QC

How We Work

Seamless Process Timeline

From initial concept to final dispatch, our structured methodology ensures transparency, quality, and on-time delivery.

1

Requirement Discussion

1–3 days

Detailed discussion on active ingredients, formulation type, batch size, and packaging needs.

2

Formulation Study

2–4 weeks

Our R&D team conducts feasibility studies and formulation development.

3

Regulatory Support

As needed

Assistance with required documentation and DCGI approvals.

4

Trial Batch & Approval

1–2 weeks

Manufacturing of a trial batch for stability testing and client approval.

5

Commercial Production

Timeline varies

Full-scale manufacturing in our WHO-GMP certified facilities.

6

QC Release & Dispatch

3–5 days

Rigorous quality control testing before final dispatch to your warehouse.

Request a Quote

Discuss your manufacturing requirements with our experts.