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WHO-cGMP
Compliant Facility
ISO 9001:2015
Certified QMS
Schedule M
Revised Compliance
DCGI Licensed
100+ Drug Approvals
IP / BP / USP
Pharmacopoeia Tested
Analytical Excellence & GLP Compliance

Precision Quality Control Testing Laboratory

Our state-of-the-art analytical testing laboratory operates under Good Laboratory Practices (cGLP), equipped with cutting-edge instrumentation ensuring every batch conforms strictly to IP, BP, and USP standards.

Assay Potency & Impurity Profiling

HPLC (Shimadzu Prominence)

Chromatographic purity > 99.8%
Residual Solvents Quantification

Gas Chromatography (GC)

USP <467> Class 1, 2, 3 compliant
Photometric Assay & Identification

UV-Vis Spectrophotometer

Double beam spectral accuracy ±0.1nm
In-Vitro Release Kinetics

Dissolution Tester (Apparatus II)

8-vessel automated multi-stage profile
ICH Accelerated & Real-Time

Walk-In Stability Chambers

Zone IVb (40°C / 75% RH & 30°C / 75% RH)
Bioburden, Sterility & Endotoxin

Class 10,000 Microbiology Lab

LAL kinetic chromogenic assay
02 · Manufacturing Infrastructure

25,000 Sq. Ft. Automated
Formulation Campus.

Our Ranpur facility operates Class 100,000 cleanrooms with PLC-controlled manufacturing lines and continuous environmental monitoring — compliant to WHO-cGMP standards.

Schedule a Plant Visit
ERVA Automated Formulation Campus
25K
Sq. Ft. cGMP Campus
100%
Monitored Air Handling
Plant Status
WHO-cGMP Validated
Ranpur, Dist. Rajkot · Gujarat
01

Granulation & Drying

GPCG fluid bed processor with APC sensor for LOD & end-point detection. Granule target D90 < 350μm.

02

High-Speed Compression

Rotary tablet press — 36 station, 120,000 tabs/hr output. Automated post-compression weight sorting.

03

Film & Enteric Coating

Perforated pan with Opadry II. Auto-spray rate, drum rpm, exhaust temp via PLC control.

04

Blister & Strip Packing

Alu-Alu cold-form and Alu-PVC blistering with online vision inspection at 120 cycles/min.

COMMERCIAL CONTRACT FORMULATION RFP

Scale Your Pharmaceutical Pipeline with
ERVA Healthcare.

Whether you are a domestic brand owner seeking third-party cGMP tableting, an institutional hospital buyer, or an overseas importer requiring export dossiers — our regulatory and technical teams deliver with speed and precision.

Dedicated formulation project manager assigned for every client
Complete Certificate of Analysis (COA) & stability documentation
Regulatory support for state FDA, DCGI & overseas MOH registrations
Flexible batch MOQs with pilot production trial batches available
< 4 Hours
RFP Response SLA
Direct technical evaluation
Flexible MOQ
Pilot to Bulk Scaling
Optimized commercial runs
CTD / ACTD
Regulatory Dossiers
Ready for MOH registrations
100% Quality
Pre-Release Testing
In-house HPLC & analytical lab