Manufacturing

Quality Manufacturing for Indian Healthcare

Synchrony Pharmaceutical operates a WHO-GMP certified manufacturing facility in Wazirpur, Delhi, equipped with modern pharmaceutical technology and quality control systems. Every medicine is manufactured following strict quality protocols and Indian pharmaceutical regulations.

Facility Location:

Block-BB Plot 280, Wazirpur, North West Delhi - 110052

Modern Pharmaceutical Manufacturing Facility

Manufacturing Process

Our production is defined by a meticulous, five-step process that guarantees quality from start to finish.

1.

Raw Material Testing

Pharmaceutical-grade ingredients tested in our QC lab before approval.

2.

Production as per approved procedures with in-process quality checks.

3.

Quality Control

Comprehensive testing including chemical analysis and stability studies.

4.

Packaging

Tamper-proof packaging with accurate labeling as per Indian regulations.

5.

Final Release

Quality Assurance approval before distribution to Indian markets.

Quality Control Laboratory

Our facility is equipped with modern analytical instruments including HPLC, UV-Visible Spectrophotometer, Dissolution apparatus, and microbiology testing equipment. Every batch undergoes complete testing before release to ensure it meets all required specifications for safety and efficacy.

Production Capabilities

We are equipped to manufacture a wide variety of dosage forms to meet diverse therapeutic needs.

Dosage Forms Manufactured:

Tablets (Coated, Uncoated, Enteric Coated)
Capsules (Hard Gelatin, Soft Gelatin)
Syrups and Suspensions
Sachets and Granules

Regulatory Compliance

We operate in full compliance with all national and international pharmaceutical guidelines.

Drugs and Cosmetics Act, 1940 - Full compliance with Indian pharmaceutical law
DCGI Regulations - Approved by Drug Controller General of India
Schedule M Compliance - GMP as per Indian regulations
WHO-GMP Standards - International manufacturing quality

WHO-GMP Certified Manufacturing