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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
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.

05 · Leadership

Leadership Grounded in
Pharmaceutical Rigor.

Our directors bring combined decades of pharmaceutical manufacturing, regulatory affairs, and commercial distribution expertise across Indian and global markets.

JT

Mr. Jagdish Tarapada

Director
+91 92276 08505
info@ervahealthcare.in
NN

Mr. Naresh Nathani

Director
+91 98244 25281
info@ervahealthcare.in
SP

Mr. Shubham Patel

Partner
+91 99980 84825
info@ervahealthcare.in

"Our commitment to quality is not just regulatory compliance — it is an uncompromising promise to every patient who depends on our medicines."

— ERVA Healthcare Leadership Board
G
Google Business
Verified Reviews
4.8 / 5

"Excellent pharmaceutical manufacturer. Professional team, timely delivery, and outstanding product documentation. Highly recommended for B2B partnerships."

04 · GLOBAL PHARMACEUTICAL SUPPLY CHAIN

Supplying Healthcare Across Continents & Borders.

From our strategic formulation campus in Ranpur (near Kandla and Mundra ports), ERVA Healthcare exports finished oral solid dosages, micro-pellets, and external preparations to institutional buyers and health ministries worldwide.

International Trade Corridor Ranpur · Gujarat

Export Packaging & Registration Support

We provide complete regulatory support including Certificate of Pharmaceutical Product (COPP), stability data for Zone IVa / IVb climatic conditions, and multilingual packaging.

ERVA Global Export Corridors
● EXPORT CORRIDOR ACTIVE Port Mundra / Nhava Sheva
Accreditations & Registrations:
WHO-cGMP Compliant ISO 9001:2015 Certified Schedule M Revised DCGI Commercial License IP / BP / USP Testing CTD / ACTD Ready
Request International Product List
8+ Nations

Africa & Sub-Saharan

Supplying essential medicines to MOH tenders across 8+ African nations including Kenya, Ethiopia, Uganda, and Tanzania with full CTD dossiers.

MOH Compliant

GCC & Middle East Region

WHO-GMP and SFDA-aligned technical documentation for regulatory-compliant supply to UAE, Saudi Arabia, Oman, and Qatar health networks.

5+ Countries

South & Southeast Asia

Distribution through established authorized pharmaceutical import partners in Myanmar, Nepal, Sri Lanka, and Philippines.

200+ Partners

Domestic Branded Generics

Serving 200+ pharmaceutical marketing enterprises across Gujarat, Maharashtra, Rajasthan, and Uttar Pradesh with dedicated batch tracking.

18+
Countries Reached
100%
CTD Dossiers Ready
Zone IVb
Stability Validated
120M+
Annual Units Output
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