31 YEARS
Since 1994
At a Glance

Manufacturing

Decades of manufacturing excellence backed by modern infrastructure and a commitment to continuous improvement.

5 Manufacturing Units
40+ APIs in Portfolio
100+ R&D Scientists
30+ Years of Excellence
Presence

Our Manufacturing Footprint

Strategically located across Telangana and Andhra Pradesh, enabling us to serve the world with quality, reliability and agility.

Vasudha Pharma manufacturing footprint across Telangana and Andhra Pradesh — Unit I to Unit V, SRCCPL and R&D Centre
World-Class Infrastructure

Manufacturing Facilities

Vasudha Pharma Chem operates an integrated network of 6 state-of-the-art production sites across Telangana and Andhra Pradesh. Spanning over 58 acres across multiple cGMP production sites, our facilities are regularly inspected and certified by top international regulatory authorities including USFDA, EDQM, PMDA (Japan), WHO-GMP, and ANVISA (Brazil).

Showing 6 of 6 Units

UNIT-1, Hyderabad

Jeedimetla
USFDA Inspected WHO-GMP KFDA / COFEPRIS
Unit-1, Jeedimetla, Hyderabad
4.0Acres Area
USFDAInspected
WHO-GMPCertified
ISO14001 / 45001

Our foundation facility specializing in active pharmaceutical ingredients and high-purity piperidine derivatives. Engineered with advanced process automation and strict cGMP protocols.

UNIT-2, Visakhapatnam

Parawada
USFDA Inspected PMDA Japan EDQM / WHO-GMP
Unit-2, Parawada, Visakhapatnam
10.6Acres Area
USFDAInspected
PMDAJapan Certified
EDQMCEP Approved

Major manufacturing hub coupled with modern pilot plants and DSIR-recognized R&D laboratories. Facilitates smooth technology transfer from milligrams to multi-ton commercial synthesis.

UNIT-3, Visakhapatnam

Parawada
USFDA Inspected (2025) PMDA Japan ANVISA / EU-WC
Unit-3, JNPC Parawada, Visakhapatnam
9.0Acres Area
USFDAInspected (2025)
EU-WCWritten Confirmation
ANVISABrazil Approved

Situated in the Jawaharlal Nehru Pharma City SEZ, this facility serves regulated Western and Asian markets with high-throughput API production and robust process safety systems.

UNIT-4, Visakhapatnam

Parawada
WHO-GMP Certified ISO 9001:2015 State DCA Licensed
Unit-4, Visakhapatnam
3.3Acres Area
WHO-GMPCertified
DCAState Licensed
Pellets& MUPS Hub

Our dedicated formulation pelletization facility engineered for sustained-release, enteric-coated, and taste-masked drug delivery systems. Equipped with state-of-the-art fluid bed processors.

UNIT-5, Visakhapatnam

Atchutapuram
USFDA / PMDA GMP EDQM CEP Approved APSEZ Mega Campus
Unit-5, Atchutapuram, Visakhapatnam
26.0Acres Area
USFDA& PMDA Audited
EDQMCEP Certified
ZLDZero Discharge

Our flagship commercial synthesis complex spread over 26 acres. Designed with integrated Zero Liquid Discharge (ZLD) environmental infrastructure, DCS process automation, and strict international cGMP compliance.

SHRI RAM CHLOROCHEM

Sangareddy
TSPCB Compliant Chlorination Centre Key Intermediates
Shri Ram Chlorochem Private Limited
5.2Acres Area
EstablishedSince 2002
IntermediatesSpecialty Hub
TSPCBConsent Compliant

Strategic group facility focused on hazardous chemical syntheses, specialty chlorination reactions, and bulk intermediate production feeding the global API value chain.

Quality & Regulatory Compliance

World-Class Quality Control & Global Assurance

Our quality control laboratories operate around the clock supporting in-process chemical controls, raw material release, finished API batch release, and comprehensive stability testing. Designed in strict compliance with current Good Manufacturing Practices (cGMP), USFDA 21 CFR Part 211, and ICH guidelines, our analytical infrastructure guarantees the therapeutic efficacy, purity, and safety of every batch delivered globally.

Global Regulatory Approvals & Certifications

Audited and accredited by the world's most stringent health authorities
10 Global Accreditations • 100% Audit Compliant
USFDA
USFDA
United States
Multiple inspections across Units 1, 2, 3, 5 and Shri Ram Chlorochem for commercial API export.
EDQM
EDQM
European Union
Certificates of Suitability (CEP) including Olmesartan Medoxomil, and EU-Written Confirmations.
PMDA
PMDA
Japan
Foreign Manufacturer Accreditation and GMP certification of intermediates and commercial APIs.
WHO-GMP
WHO-GMP
Geneva / Global
World Health Organization Good Manufacturing Practices pre-qualification across active sites.
MFDS Korea
MFDS (KFDA)
South Korea
Approved Korean Drug Master Files (KDMF) and periodic cGMP compliance audits.
COFEPRIS
COFEPRIS
Mexico
Approved for supply of essential cardiovascular and antihistamine bulk drugs to Mexico.
ANVISA
ANVISA
Brazil
Brazilian National Health Surveillance Agency cGMP certification with regular renewals.
CDSCO
CDSCO
India
National licensing authority with Written Confirmations for EU exports under Falsified Medicines Directive.
ISO Standards
ISO Standards
Quality & EHS
Triple certified: ISO 9001:2015 (Quality), ISO 14001:2015 (Environment) & ISO 45001:2018 (Safety).
EcoVadis
EcoVadis
Sustainability
Recognized for excellence in environmental stewardship, ethical business practices, and labor rights.

Partner with a trusted API manufacturer

Whether you need high-quality APIs, intermediates or custom manufacturing support, our team is ready to collaborate.

Contact Our Team